Skip to main content

ORIGINAL RESEARCH article

Front. Aging Neurosci., 20 September 2022
Sec. Parkinson’s Disease and Aging-related Movement Disorders
Volume 14 - 2022 | https://doi.org/10.3389/fnagi.2022.931048

Extended effects of a wearable sensory prosthesis on gait, balance function and falls after 26 weeks of use in persons with peripheral neuropathy and high fall risk—The walk2Wellness trial

  • 1RxFunction Inc., Eden Prairie, MN, United States
  • 2Department of Rehabilitation Medicine, Medical School, University of Minnesota, Minneapolis, MN, United States
  • 3Recanati School for Community Health Professions, Faculty of Health Sciences, Ben Gurion University of the Negev, Beersheba, Israel
  • 4M Health Fairview, Minneapolis, MN, United States
  • 5Baylor College of Medicine, Houston, TX, United States
  • 6Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Roslindale, MA, United States
  • 7Division of Gerontology, Beth Israel Deaconess Medical Center, Boston, MA, United States
  • 8Harvard Medical School, Boston, MA, United States
  • 9Minneapolis Department of Veterans Affairs Health Care System, Minneapolis, MN, United States
  • 10College of Saint Mary, Omaha, NE, United States

Background: We recently reported that individuals with impaired plantar sensation and high fall risk due to sensory peripheral neuropathy (PN) improved gait and balance function following 10 weeks of use of Walkasins®, a wearable lower limb sensory prosthesis that provides directional specific mechanical tactile stimuli related to plantar pressure measurements during standing and walking (RxFunction Inc., Eden Prairie, MN, United States). Here, we report 26-week outcomes and compare pre- and in-study fall rates. We expected improvements in outcomes and reduced fall rates reported after 10 weeks of use to be sustained.

Materials and methods: Participants had clinically diagnosed PN with impaired plantar sensation, high fall risk (Functional Gait Assessment, FGA score < 23) and ability to sense tactile stimuli above the ankle at the location of the device. Additional outcomes included 10 m Gait Speed, Timed Up and Go (TUG), Four-Stage Balance Test, and self-reported outcomes, including Activities-Specific Balance Confidence scale and Vestibular Disorders Activities of Daily Living Scale. Participants tracked falls using a calendar.

Results: We assessed falls and self-reported outcomes from 44 individuals after 26 weeks of device use; 30 of them conducted in-person testing of clinical outcomes. Overall, improvements in clinical outcomes seen at 10 weeks of use remained sustained at 26 weeks with statistically significant increases compared to baseline seen in FGA scores (from 15.0 to 19.2), self-selected gait speed (from 0.89 to 0.97 m/s), and 4-Stage Balance Test (from 25.6 to 28.4 s), indicating a decrease in fall risk. Non-significant improvements were observed in TUG and fast gait speed. Overall, 39 falls were reported; 31 of them did not require medical treatment and four caused severe injury. Participants who reported falls over 6 months prior to the study had a 43% decrease in fall rate during the study as compared to self-report 6-month pre-study (11.8 vs. 6.7 falls/1000 patient days, respectively, p < 0.004), similar to the 46% decrease reported after 10 weeks of use.

Conclusion: A wearable sensory prosthesis can improve outcomes of gait and balance function and substantially decreases incidence of falls during long-term use. The sustained long-term benefits in clinical outcomes reported here lessen the likelihood that improvements are placebo effects.

Clinical trial registration: ClinicalTrials.gov, identifier #NCT03538756.

Introduction

Persistent problems with gait and balance function may lead to falls, fractures, and other serious injuries in older adults (Bergen et al., 2016; Ganz and Latham, 2020; Moreland et al., 2020). In fact, clinical observations on the problem of falls and fall prevention go back to at least 1948 when Sheldon (1948) presented data in The Lancet on “Liability to Falls” in older adults, concluding that falling was “a clinical problem which has never received the attention it deserves.” Today, we appreciate that causes of falls are complex and require a multifactorial clinical approach to arrive at a correct diagnosis and to provide specific and relevant therapeutic interventions (Cohen et al., 2015).

To address the problem of falls in older adults, various clinical practice guidelines for falls prevention and management have been developed (Montero-Odasso et al., 2021). The Centers for Disease Control and Prevention (CDC), for example, has established “STEADI” (STEADI, 2021), an evidence-based initiative to address fall prevention based on a curation of decades of research activities (Stevens and Phelan, 2013). At this time, advice provided through the STEADI initiative includes “Talk to your doctor”; “Do Strength and Balance Exercises”; “Have Your Eyes Checked”; and “Make Your Home Safer” (CDC, 2021). At a minimum, health care providers should screen their patients for fall risk, including older adults and individuals with neurodegenerative diseases that affect balance function. Simple interventions that should be considered to help reduce the risk for falls include medication management and vitamin D supplements to improve bone, muscle, and nerve health (Bergen et al., 2016). Further treatment of gait and balance issues may involve use of canes, walkers, and rehabilitation interventions with balance exercises (Richardson et al., 2001; Halvarsson et al., 2013; Melzer and Oddsson, 2013; Ganz and Latham, 2020), including Tai-Chi (Li and Manor, 2010; Manor et al., 2014; Quigley et al., 2014). Any functional benefits related to fall rates and gait function after long-term use of bilateral ankle foot orthoses appear limited (Wang et al., 2019).

In addition to other age-related risk factors, sensory peripheral neuropathy (PN), leading to impaired plantar sensation, is an independent risk factor for falls (Richardson and Hurvitz, 1995; Koski et al., 1998; Reeves et al., 2021), irrespective of whether the underlying cause is due to diabetes (Mustapa et al., 2016; Vinik et al., 2017), chemotherapy (Winters-Stone et al., 2017), or an unknown factor (Riskowski et al., 2012). The prevalence of PN in the United States population for those over age 40 is nearly 15% (Gregg et al., 2004) and 28.4% in persons with diabetes (Hicks et al., 2021). The incidence of injuries due to falls is 15 times higher in patients with diabetic PN than in healthy individuals (Cavanagh et al., 1992). Furthermore, polyneuropathy contributes independently to functional impairments, including difficulty walking and a tendency to fall (Hoffman et al., 2015), and those individuals more often incur fall-related injuries (Hanewinckel et al., 2017). A prospective study of older individuals with PN found that 65% fell during a one-year period and 30% reported an injury from a fall (DeMott et al., 2007).

Mechanoreceptors play an important role in proprioception (Fallon et al., 2005; Vaughan, 2021) and loss of sensory information from the lower limbs, including plantar mechanoreceptors alters balance performance (Meyer et al., 2004a,b). Furthermore, this sensory impairment affects the automaticity of walking, thereby increasing the need for cognitive attention to gait and mobility activities (Paul et al., 2005; Clark et al., 2014; Clark, 2015). Furthermore, several studies have reported problems with gait and balance function and the increased risk of falls in patients with PN (Menz et al., 2004; DeMott et al., 2007; Dixon et al., 2017; Lipsitz et al., 2018).

Additionally, low gait speed is a risk factor for falls (Studenski et al., 2003; Montero-Odasso et al., 2005), is an indicator of frailty (Kim et al., 2019), and is even a predictor of hospitalization and disability (Cesari et al., 2005; Dumurgier et al., 2009) as well as survival (Studenski et al., 2011). In fact, interventions designed to improve gait speed may actually increase survival (Hardy et al., 2007). Older adults with sensory impairment related to PN show a decline in gait speed that is four times higher than in healthy aging (Buracchio et al., 2010; Lipsitz et al., 2018).

Although strength and balance training in patients with PN may help reduce fall risk falls (Ites et al., 2011; Tofthagen et al., 2012; Streckmann et al., 2014; Morrison et al., 2018), strength training in patients with PN appears to have less impact on balance (Streckmann et al., 2014). Its effects are mainly compensatory and do not address impaired somatosensation, the root cause of balance problems related to PN. Furthermore, balance training activities must be specific (Oddsson et al., 2007) and must be conducted with sufficient intensity and frequency (Lipsitz et al., 2019) to be helpful, or benefits will be limited or absent (Kruse et al., 2010; Lipsitz et al., 2018, 2019). Clear guidelines regarding frequency of balance exercises are currently lacking although three sessions a week may be a minimum necessary to see an improvement (Kruse et al., 2010). Thus, although “Falls can be prevented” (CDC, 2021), they continue to be a large problem in older adults, indicating a continued need for novel solutions.

We recently reported from our multi-site clinical trial (walk2Wellness, NCT #03538756) that individuals with PN and a high risk of falls improved their Functional Gait Assessment (FGA) scores, (Wrisley et al., 2004), Gait Speed, and Timed Up and Go times following 10 weeks of home-based use of a wearable sensory prosthesis intended to substitute nerve function related to impaired plantar sensation (Figure 1, Walkasins by RxFunction Inc., Eden Prairie, MN, United States), (Oddsson et al., 2020). Previously, we found similar meaningful improvements in FGA scores and gait speed in participants with PN in a randomized crossover trial conducted in-clinic (Koehler-McNicholas et al., 2019), findings that were recently referred to as “presumably emulating” signals by fast-adapting cutaneous afferents (Vaughan, 2021). We also reported a decrease in the number of fall risk factors as well as fall rate from baseline to 10 weeks for individuals who reported falls in the 6 months preceding study participation (Oddsson et al., 2020).

FIGURE 1
www.frontiersin.org

Figure 1. (Left) The two components of the Walkasins prosthetic device, the pressure sensitive flexible foot pad that is placed in the shoe and connects to the leg unit that contains a rechargeable battery, a microprocessor, supporting electronics, and four mechanical tactile stimulators. The embedded software algorithm evaluates pressure data and activates the mechanical tactile stimulators at relevant times during standing and walking to signal balance-related information to the afferent nervous system. (Right) A Walkasins user wearing the device in the process of turning it on. The Walkasins system is worn bilaterally (unilateral components depicted).

Here we report extended long-term use data from the walk2Wellness trial for 44 participants after 26 weeks of Walkasins use. Furthermore, we analyzed falls during the 26 weeks of device use and compared to patient self-reports of falls from the 6 months preceding participation in the study. We expected improvements in clinical outcomes and lower fall rate seen after 10 weeks (Oddsson et al., 2020) to be sustained at 26 weeks.

Materials and methods

Detailed descriptions of materials and methods have been reported previously (Oddsson et al., 2020), and are summarized below. The measures we use have been validated (Oddsson et al., 2020) and our primary outcome measure, the FGA, is recommended for assessment of walking balance in adults with neurologic conditions by current physical therapy Clinical Practice Guidelines (Moore et al., 2018). The walk2Wellness study is registered at ClinicalTrials.gov (#NCT03538756). Figure 1 shows a picture of the Walkasins device components with a brief description of its functionality.

Participants

The walk2Wellness clinical trial received approval for human subject research from Advarra IRB (formerly Quorum Review) for four sites and from the IRB Subcommittee, the Subcommittee on Research Safety, and the Research and Development Committee of the Minneapolis VA Health Care System (MVAHCS). Recruitment for the walk2Wellness trial began in October 2018 and ended at the last site in April 2021. Because of COVID-19 disruptions, the study ended earlier than planned at four sites; the fifth site completed the trial but with a reduced enrollment goal. Study site team members posted fliers at community businesses and clinics to advertise the trial; in addition, some of the sites received referrals from physicians who were informed about the study.

To participate in the trial, individuals met the following inclusion criteria: male or female; ages 21–90; a formal diagnosis of sensory PN prior to participating in the study as indicated by their medical record or a letter by a physician; self-reported problems with balance; ability for transfers or ambulation on level surfaces at fixed cadence as assessed by trained study personnel; FGA score < 23, the cut-off score for high fall risk (Wrisley and Kumar, 2010); ability to understand and provide informed consent; foot size to allow the Walkasins device to function properly, and ability to complete all functional outcome measures without the use of an assistive device in order to ensure sufficient motor function. Participants could use an assistive device at their discretion during their daily activities.

Individuals were excluded if they were unable to perceive the tactile stimuli from the Walkasins leg unit (Figure 1) or if they used an ankle-foot orthosis for ambulation that prevented donning the device. In addition, individuals having any of the following conditions were excluded from participation: acute thrombophlebitis; deep vein thrombosis; untreated lymphedema; a lesion of any kind, swelling, infection, inflamed area of skin, or eruptions on the lower leg near placement of the device; foot or ankle fractures; severe peripheral vascular disease; or any musculoskeletal or neurological condition that would prohibit use of the device, as determined by a clinician. Because of a potential to overload the pressure sensors in the foot pad, individuals weighing over 136 kg (300 lbs) were excluded from participation. The criteria to participate in the study were similar to receiving a prescription for the device in a clinic. Potential participants also agreed not to initiate any balance training (e.g., Tai-Chi, etc.) or balance-related therapy during the first 10 weeks of the trial (Oddsson et al., 2020). Furthermore, participants were blinded to their outcomes during the trial and not shared by study personnel.

Study procedures and outcome measures

Before undergoing any study-related procedures, individuals signed the IRB-approved consent form and HIPAA authorization. after enrollment, site staff tested whether participants were able to perceive the tactile stimuli from the Walkasins leg unit. Anyone unable to feel the tactile stimuli was excluded from continued participation in the study. Individuals who were able to feel the tactile stimuli from the Walkasins leg unit bilaterally then completed a medical history form to assess common health issues and systemic diseases. They also provided information on falls they had experienced in the previous 6 and 12 months, including the number of falls and any injuries they sustained as a result. In addition, participants provided a list of their medications (medication name, indication, dose, and frequency), which was updated over the course of the study.

Participants then completed the Activities-Specific Balance Confidence (ABC) Questionnaire (Powell and Myers, 1995) to assess levels of balance self-confidence and the Vestibular Activities of Daily Living Scale (VADL), (Cohen et al., 2000) to evaluate the effects of vertigo and balance disorders on their ability to perform everyday activities independently. At baseline, weeks 10 and 26, site personnel also assessed participants using the Weinstein Enhanced Sensory Test (WEST) monofilament foot test (0.5, 2, 10, 50, and 200 g), as described previously (Oddsson et al., 2020). Staff also performed a vibration sensation test using a Rydel-Seiffer Tuning Fork to document loss of sensation (Kästenbauer et al., 2004; Oddsson et al., 2020). Scoring values ≤4 at the first metatarsal joint is categorized as abnormal (Kästenbauer et al., 2004).

During the baseline visit, participants donned the Walkasins devices and performed a standardized set of standing and walking balance activities focused on orientation and familiarization with the device, referred to as the Walkasins Learning Protocol (Koehler-McNicholas et al., 2019; Oddsson et al., 2020). Trained site personnel then assessed participants on the FGA, 10-Meter Walk Test (Perera et al., 2006), Timed Up and Go (TUG) (Mathias et al., 1986), and 4-Stage Balance Test (CDC, 2021). The clinical outcomes were standardized and performed by study personnel who were trained by one of the investigators (DW). A sponsor representative conducted observation visits periodically during the study to ensure standardization across the sites (LJ).

After finishing the clinical outcome tests, participants completed the following self-reported outcome measures to provide information about their quality of life, pain level, and engagement in social activities: Patient Health Questionnaire (PHQ-9) (Kroenke et al., 2001), PROMIS Pain Interference Short Form 6b (Askew et al., 2016), PROMIS Pain Intensity Form 1a, Ability to Participate Short Form 8a (Hahn et al., 2016b), and Satisfaction with Participation in Social Roles Short Form 8a (Hahn et al., 2014, 2016a). At the conclusion of the baseline visit, site staff members trained the participants on caring for the device.

Participants left the baseline visit with the device and a calendar on which to note any fall events they experienced as well as their use of Walkasins. For consistency across sites, we used the World Health Organization’s definition of a “fall”: “A fall is an event which results in a person coming to rest inadvertently on the ground or floor or other lower level.” When participants reported falls, study staff recorded the following: the fall date; severity (no injury, minor injury, or major injury); the level of treatment the individual sought or received, if any; the cause or causes of the fall (environmental factor, lost balance, lost consciousness, lost strength/felt weak, slipped, tripped, on new medication, other, unknown); and a description of the fall.

Unless prevented from doing so because of COVID-19 site restrictions, participants returned for in-person visits at weeks 2, 6, 10, and 26. These visits followed most of the same procedures as the baseline visit: balance questionnaires, clinical assessments, and self-reported outcome measures. As we have previously reported (Oddsson et al., 2020) we calculated ABC to FGA ratios at each assessment to measure the degree of internal self-perception of balance capability (ABC score) in relation to the externally observed walking balance performance (FGA score). We noted that a ratio of around 3.3 would be “expected” based on the maximum scores of the two scales. This construct aligns with a multifactorial causation model for falls emphasizing the importance of a “Realistic Appraisal of One’s Own Abilities,” (Hadjistavropoulos et al., 2011).

Between the in-person visits at weeks 10 and 26, study sites contacted participants via telephone at weeks 14, 18, and 22 to remind them of study requirements and to collect follow-up information regarding health changes, falls, adverse events, pain scores, device usage, and device functioning, as well as whether they had begun any physical therapy for their balance problems. If participants reported adverse events and/or falls during these contacts, site personnel recorded the details on the appropriate case report forms in REDCap Cloud, the electronic data capture system used in the study1 (Encinitas, CA, United States).

Statistical analysis and availability of data

An analysis of outcomes after 2, 6, and 10 weeks, with 10 weeks being the primary endpoint, was presented earlier (Oddsson et al., 2020). Here we focus on outcomes after extended long-term device use and compare outcomes to baseline for individuals participating in 26 weeks of device use. Graphical data from 2, 6 and 10 weeks are provided below for illustration. We calculated descriptive statistics (mean and standard deviation or median as appropriate) for all variables and tested for normality with the Shapiro-Wilk’s test. We applied the two-proportion Z-test to compare proportion-based measures. We conducted a post hoc analysis to compare participants at baseline who reported falls in the previous 6 months (Pre-Fallers, n = 25) to those who did not (Pre-Non-Fallers, n = 19). Their baseline characteristics were compared using a t-test for independent samples or a Mann-Whitney U test if data was not normally distributed based on a Shapiro-Wilk’s test.

To compare baseline variables to those after 26 weeks of device use, we conducted a t-test for dependent samples or Wilcoxon signed-rank test in case variables were not normally distributed. We applied a Bonferroni’s adjustment of significance levels for correlated measures, ranging from p < 0.0167 (0.05/3 for three comparisons) for a full correction (non-correlated measures, r = 0) and p < 0.05 for perfectly correlated measures (r = 1) (Uitenbroek, 1997). We calculated effect sizes using Cohen’s drm according to recommendations by Lakens (2013) and interpreted them according to Cohen (1988), i.e., 0.2 represents a small effect, 0.5 a medium effect, and 0.8 a large effect size. Ninety-five percent confidence intervals of effect sizes were estimated according to Algina et al. (2005).

We performed statistical analysis with the Analysis-ToolPak module in Microsoft Excel 2016 and the Real Statistics Resource Pack software, release 6.8 (Zaiontz, 2020). Baseline characteristics of participants in the study from the four clinical sites are presented in Table 1. We have pooled the data for the continued analysis presented here. The raw data supporting the conclusions of this article will be made available to qualified researchers without undue reservation.

TABLE 1
www.frontiersin.org

Table 1. Characteristics of the 44 individuals from the four different clinical sites enrolled in the study who reached 26 weeks of participation.

Results

Enrollment and allocation

Our previous report with 45 participants at the 10-week primary endpoint (Oddsson et al., 2020) was published early due to the unknown circumstances at the time related to COVID-19, which had caused recruitment holds and suspension of in-person testing activities at the research sites. Over time, the trial continued with the enrollment of additional participants who are part of the current report as illustrated in the flow chart in Figure 2. Figure 2 shows the flow chart for the study as it was continued from the 10-week primary endpoint assessment that we have previously reported (Oddsson et al., 2020). Text boxes with dashed lines in Figure 2 indicate enrollment numbers for the initial 10-week report.

FIGURE 2
www.frontiersin.org

Figure 2. Flowchart of the walk2Wellness trial. Data for the primary endpoint at 10 weeks, shown to the right for reference, were published earlier (Oddsson et al., 2020). Due to COVID-19 site lockdowns, in-person outcomes could be assessed from 30 of the 44 participants. Self-reported outcomes and fall events were assessed from all 44 participants who reached the 26-week follow-up visit.

Of the 85 individuals who were assessed for eligibility, a total of 69 participants were enrolled in the trial (17 more than in previous report, cf. Figure 2). Sixty participants took part in the 2-week follow up visit, 55 in the 6-week follow-up visit, and 51 in the 10-week follow-up visit (six more than in the previous report). Eleven of the 18 participants who discontinued interventions through the 10-week follow-up visit stopped participation due to circumstances related to COVID-19 (cf. Figure 2). (Note: due to the timing of study initiation at Johns Hopkins and the onset of the pandemic, the three participants enrolled at the site were unable to complete most in-person assessments. When the situation did not improve, the sponsor decided to terminate Johns Hopkins as a research site. None of the participants had completed follow-up datasets through week 10, so their results were not included in this analysis.)

Forty-four of the 51 participants who reached the 10-week follow-up assessment were analyzed after their 26-week assessment. Due to circumstances related to COVID-19, including lockdowns at the research sites, 14 of the 44 participants were unable to participate in the 26-week in-person outcomes testing (FGA, 10MWT, TUG, and 4-Stage Balance Test). All 44 participants, however, were assessed on self-reported outcomes over the phone, and all 44 participants provided reports of falls throughout the 26-week period. Consequently, we report baseline assessment of clinical outcomes for all 44 participants, comparing those who reported falling in the prior 6 months (Pre-Fallers) to those who did not (Pre-Non-Fallers). We also present data over time for the 30 participants who completed the 26-week in-person assessment (weeks 0, 2, 6, 10, and 26, Figure 2), comparing the baseline assessments of those 30 participants to their 26-week assessment.

Seven of the 44 participants discontinued the intervention after the 10-week assessment (cf. Figure 2); one passed away; two had been enrolled in solely the 10-week protocol; three expressed device dissatisfaction, and one experienced an unrelated adverse event.

Baseline characteristics and outcomes

Baseline characteristics for the 44 individuals who were evaluated at 26 weeks are shown in Table 1 and were substantially similar to those reported previously (Oddsson et al., 2020). Participants across all sites were pooled for the continued analysis.

The baseline characteristics of the 44 participants are shown in Table 2. Characteristics are also reported separately for participants who reported falling in the 6 months preceding the study (Pre-F, n = 25) and participants who did not report a fall (Pre-NF, n = 19). Overall, characteristics reported previously for participants entering the trial were maintained (Oddsson et al., 2020) except for some substantiated differences between the Pre-F and Pre-NF participants that were now statistically significant (Table 2). In addition to previous observations, baseline self-selected gait speed and ABC scores were significantly different between the Pre-F and Pre-NF groups, 0.83 vs. 0.97 m/s and 57.8 vs. 69.6%, respectively (Table 2). A higher observed mean value in PHQ-9 score for the Pre-F group was nearly statistically significant (5.7 vs. 3.3, respectively, p = 0.052). Mean values for all PROMIS measures were near 50, and any differences were well within 10 (Table 2) corresponding to one standard deviation for these measures, indicating any observed differences were minor (Askew et al., 2016; Hahn et al., 2016a,b).

TABLE 2
www.frontiersin.org

Table 2. Baseline characteristics for participants reaching the 26-week assessment (n = 44).

Clinical outcomes

Improvements in FGA scores were seen across all individuals, irrespective of their baseline FGA scores and appeared similar after 2-, 6-, 10-, and 26-weeks of device use (Figure 3). This finding is indicated by the regression lines in Figure 3 being shifted above the line of equality. Figure 3 also illustrates similar improvements in FGA scores for the Pre-F group and the Pre-NF group (filled vs. open symbols). Interestingly, the slope of the regression line was <1 at all assessments indicating larger improvements in the lower range of baseline FGA scores mostly representing Pre-F group participants (cf. Table 3 and further below). After 26 weeks of device use, FGA scores increased across all individuals from 15.0 to 19.2 (p < 0.00001, Table 3) indicating a large effect size (Cohen’s drm = 1.38, Table 3). Furthermore, self-selected gait speed increased from 0.89 m/s to 0.97 m/s (p = 0.02), a medium effect size (Cohen’s drm = 0.49); and the 4-Stage Balance Test improved from 25.6 s to 28.4 s (p < 0.01), representing a small effect size (Cohen’s drm = 0.32). An increase seen in fast gait speed (1.30 to 1.37 m/s) did not reach statistical significance (p = 0.07). Changes in Rydel-Seiffer tuning fork testing scores suggested a small decrease in sensitivity at the site of the lateral malleolus (mean 3.8 to 3.2, p = 0.032, Cohen’s drm = 0.32), while a noted decrease at the MTP joint did not reach statistical significance (p = 0.07).

FIGURE 3
www.frontiersin.org

Figure 3. Comparing FGA scores at baseline (horizontal axes) with assessments after 2 (A), 6 (B), 10 (C), and 26 (D) weeks (vertical axes) of device use. Open symbols represent pre-study non-fallers and filled ones are pre-study fallers. Dashed lines show regression line for the whole group. Forty-four participants completed in clinic outcomes testing up to 10 weeks (primary endpoint), and 30 participants completed the 26-week assessment in person. Scores above line of equality indicate improvements and below a decrement in FGA score compared to baseline scores. Notice that regression line slopes are less than 1 indicating slightly larger improvements in FGA score for those with lower baseline scores. Overall, improvements observed after 2 weeks of use appeared sustained throughout the 26 weeks of use.

TABLE 3
www.frontiersin.org

Table 3. Clinical outcomes and Rydel-Seiffer vibration sensation screening for the 30 individuals who were able to complete all in-person assessments at baseline and after 26 weeks as well as the subgroups of Pre-Fallers and Pre-Non-Fallers.

The Pre-F cohort (n = 18) improved their mean FGA score from 13.7 at baseline to 18.1 at 26 weeks (p < 0.0001, Table 3) representing a large effect size (Cohen’s drm = 1.58). Their observed increases in self-selected gait speed from 0.82 to 0.90 m/s and from 1.13 to 1.23 m/s for fast gait speed did not reach statistical significance (p = 0.12 and p = 0.07, respectively). The Pre-F group showed a decrease in vibration sensation at the first MTP joint (mean 2.9 to 1.8, p < 0.005) and at the lateral malleolus that did not reach statistical significance (mean 3.75 to 3.25, p = 0.07).

The Pre-NF group (n = 12) increased their mean FGA score from 17.0 at Baseline to 20.8 at 26 weeks (p < 0.004, Cohen’s drm = 1.23, Table 3). A small increase in self-selected gait speed from 1.00 m/s to 1.08 m/s did not reach statistical significance (p = 0.06). Other clinical outcomes, including Rydel-Seiffer tuning fork sensitivity testing scores, remained unchanged at 26 weeks compared to baseline (Table 3).

The mean values of all in-person outcomes across the 26 weeks of device use for all participants are depicted in Figure 4 and are shown separately for the Pre-F and the Pre-NF groups. In general, the behavior over time of the two subgroups was qualitatively similar, although the Pre-NF group consistently performed better than the Pre-F cohort.

FIGURE 4
www.frontiersin.org

Figure 4. Averages of clinical outcomes across the in-person assessments at baseline (0), 2, 6, 10, and 26 weeks for the 30 participants (blue lines and symbols) who were able to be tested in clinic after 26 weeks of device use for the in-clinic outcomes FGA (A), TUG (B), gait speed (C,D), and the Four-Stage Balance test (E). Gray symbols and lines represent the pre-study non-fallers (n = 12 of 30) and orange lines and symbols represent pre-study fallers (n = 18 of 30). Notice that most improvements appeared to peak after 6–10 weeks of device use, followed by a leveling off until 26 weeks.

Self-reported outcomes, device use and Activities-Specific Balance Confidence to Functional Gait Assessment ratios

Self-reported outcomes for the 44 participants who completed assessments through 26 weeks are shown in Table 4. Across all participants, a slight but statistically significant increase was seen in PROMIS Ability to Participate scores after 26 weeks of device use (49.9 to 52.6, p < 0.05). All baseline values were maintained at 26 weeks for the Pre-F group while we noted an increase in the PROMIS Satisfaction with Social Roles scores (49.9 to 55.5, p < 0.006) for the Pre-NF group.

TABLE 4
www.frontiersin.org

Table 4. Results from self-reported outcomes for the 44 individuals who completed all assessments.

Participants documented their weekly device use in a calendar and were asked to report it back during phone calls at weeks 14, 18, 22, and 26. Their average reported weekly device use was 5.1 ± 0.4 days. Participants reporting that they used the device weekly either “Every Day” or “At least 5 Days” was 71.8 ± 10.5%. An average of 94.8 ± 3.3% of reporting participants stated they used the device “1–2 Days” or more per week.

We also sought to monitor participants’ self-perceived balance confidence (Lajoie and Gallagher, 2004) in relation to their assessed gait function performance over time in the trial by measuring changes in the ABC to FGA ratio, which is shown in Figure 5. Figure 5 illustrates two observations. First, the ABC/FGA ratio for the overly confident individuals gradually decreased from high values at baseline to week 6 when the ratio essentially aligned with the low self-confidence participants, who maintained a consistent ABC/FGA ratio of about 3.5 throughout the 26-week period of the trial (Figure 5, left y-axis). Second, both groups of participants increased their FGA scores in a similar fashion although the overly confident participants showed higher levels of improvement in their FGA scores (Figure 5, right y-axis).

FIGURE 5
www.frontiersin.org

Figure 5. Illustration of changes in ABC/FGA ratio (left axis, solid lines), an indication of self-perceived balance confidence in relation to externally observed gait function performance, for participants with baseline ABC scores >67% (high balance-confidence, orange triangles) and those with ABC scores ≤67% (low balance-confidence, blue circles). The associated changes over time in FGA scores for the same two groups are also shown (right axis, dashed lines). Notice that both groups had similar FGA scores at baseline, which led to a dramatic difference in the ABC/FGA ratio at baseline. Over time, the ratio for the high balance-confidence participants gradually decreased and aligned with the low balance-confidence group at ∼3.5, mainly due to an increased FGA score and a maintained ABC score. The low balance-confidence group maintained an ABC/FGA ratio ∼3.5 throughout the 26 weeks associated with a proportional increase in ABC and FGA scores. Interestingly, the high balance-confidence group showed a higher increase in FGA score than the low balance-confidence group.

Falls data

Falls were reported throughout the 26-week period for all 44 participants and separately for the Pre-F (n = 25) and Pre-NF (n = 19) groups, respectively (Table 5). The 44 participants reported a total of 53 falls over 6 months prior to participating in the trial while 39 falls were documented during the 26 weeks of the trial, corresponding to a pre-study mean fall rate of 6.7 falls/1000 patient days (median = 5.6 falls/1000 patient days) and a post study mean fall rate of 4.8 falls/1000 patient days (median = 0 falls/1000 patient days). Wilcoxon Signed Rank test was used to compare pre- and post-study fall rates since the data was not normally distributed (Shapiro–Wilk W-statistic = 0.82, p < 0.0001). Across all participants, the median of the post-study fall rate was lower than the pre-study fall rate (Table 5, p = 0.044), reflecting a 28% decrease in fall rate. Of the 44 participants, 25 had fallen in the past 6 months (Pre-F); and after 26 weeks, 20 of the 44 participants had reported falling. Overall, 31 of the 39 falls required no treatment while eight falls (∼20%) required treatment with four of those (∼10%) causing severe injury (two fractures) (Table 5).

TABLE 5
www.frontiersin.org

Table 5. Parameters related to falls and fall risk assessed at baseline and at 26 weeks.

The 25 participants in the Pre-F cohort reported 31 falls after 26 weeks compared to 53 falls pre-study corresponding to a pre-study fall rate of 11.8 falls/1000 patient days (median = 11.1), which decreased to 6.7 falls/1000 patient days at 26 weeks (median = 5.0), a 43% decrease in fall rate (p = 0.0043). Of the 25 Pre-F participants, 12 did not fall during the study, a 48% statistically significant decrease in number of fallers (p < 0.0001). Of the 31 falls experienced by the Pre-F cohort, six (∼20%) required treatment (Table 5). Three of the four falls that led to severe injury occurred in the Pre-F group.

Seven of the 19 Pre-NF participants reported falling during the trial (p < 0.0001) leading to an increase in fall rate from zero to 2.3 falls/1000 patient days at 26 weeks that was statistically significant (p = 0.023). A total of eight falls were reported by the seven Pre-NF participants who fell during the study (Table 5). Two of the eight falls in the group required treatment, and one fall led to a severe injury.

Figure 6 illustrates the cumulative sum of falls based on 6-month pre-study fall reports from the participants and the falls recorded by the Pre-F cohort during the trial. The 53 pre-study falls were randomly distributed across the 6-month pre-study period for illustration purposes since the exact time of their occurrence prior to the trial were not known (see Figure 6). Note that 53 falls over a period of 6 months corresponds to 53/180∼0.29 falls/day, which becomes the slope of the blue regression line in Figure 6, irrespective of the random distribution of the pre-study falls. The in-study falls are presented on the day they occurred according to participant reports (see Figure 6). The in-study decrease of falls quantified in Table 5 can be visually observed over time in Figure 6 as a lower slope for the best fit regression line (blue-dotted line pre-study vs. orange-dotted line in-study). It should be noted that the lower slope appears to begin after about 20 days of device use.

FIGURE 6
www.frontiersin.org

Figure 6. Accumulated number of falls reported 6 months pre-study (blue trace and blue dotted linear regression line) and falls documented in-study (orange trace and orange dotted regression line). The 53 falls reported for the prior 6 months would correspond to 0.29 falls/day (53/180∼0.29), which represents the slope of the regression line (blue trace). For illustration purposes, the 53 pre-study falls were randomly distributed across the 6 months since their exact time occurrence was unknown. In-study falls are shown as they occurred and were reported by participants throughout the 26 weeks. Notice how the rate of in-study falls appear to begin deviating from pre-study fall rate (slope of dotted blue line) after approximately 20 days of device use.

Discussion

Key findings

Walkasins is a device that provides mechanical tactile stimuli related to foot pressure for individuals with PN and gait and balance problems. Overall, our findings from analyzing outcomes after 26 weeks of wearing Walkasins show that improvements in outcomes seen after 10 weeks of use are sustained longer term (Oddsson et al., 2020). The FGA score was improved from 15.0 at baseline to 19.2 after 26 weeks of device use across all participants, a large effect size (Cohen’s drm = 1.38) and an increase that is beyond the MCID for community-dwelling older adults (Beninato et al., 2014). Interestingly, these improvements were seen for individuals across the full range of baseline FGA scores, from the lowest of 7 to the highest of 22 (Figure 3) with a tendency to be higher for individuals in the lower FGA range. Furthermore, similar improvements were seen for the Pre-F and Pre-NF cohorts. Moreover, the 46% decrease in fall rate, compared to pre-study falls we reported after 10 weeks of use, was sustained at 43% after 26 weeks, an important observation further discussed below. Weekly device use continued to be high and similar to after 10 weeks [5.1 vs. 5.3 days/week, respectively (Oddsson et al., 2020)].

All clinical outcomes improved compared to baseline, but changes in TUG and 4-Stage Balance did not reach statistical significance, likely because the study was underpowered for these measures (Table 3). Previous work has found that older individuals with diabetic PN walk slower than their healthy cohort (Menz et al., 2004), and older adults with peripheral sensory impairment show a 0.046 m/s/year. decline in gait speed (Lipsitz et al., 2018). This decrease is more than 3.5 times higher than declines reported in healthy aging (Buracchio et al., 2010). With this in mind, it is encouraging to report a statistically significant 0.08 m/s increase in gait speed gait speed across all participants in this trial, which is beyond a small meaningful change (0.05 m/s) and close to the range for a substantial meaningful change (0.10 m/s) (Perera et al., 2006).

Participants had a decrease in sensitivity to vibration, an overall small decrease at the lateral malleolus and a larger change at the MTP joint in the Pre-Faller group. Such changes did not occur at the 10-week assessment (Oddsson et al., 2020). This decrease in tuning fork vibration perception may indicate a progression of some participants’ PN and increased sensory loss. In spite of such changes, none of the participants stated that they were unable to perceive the stimuli provided by the device, suggesting they were still benefiting from its use as confirmed by improved clinical outcomes.

Balance exercise interventions and their limitations

We can compare our findings to interventions using different forms of physical exercise in patients with PN since we see similar improvements in outcomes from simply wearing the device in the current trial. Several review studies conclude that balance training is “the most effective exercise intervention” (Ites et al., 2011; Tofthagen et al., 2012; Streckmann et al., 2014; Morrison et al., 2018), while strength training in patients with PN appears to have less impact on balance (Streckmann et al., 2014), likely due to lack of specificity related to balance (Oddsson et al., 2007). Although such interventions may improve balance outcomes, effects are essentially compensatory since they do not address the root cause of the balance problem in these patients, namely their impaire plantar sensation due to PN. Furthermore, any exercise activity would need to be maintained on a regular basis long-term or benefits would gradually be lost (Melzer and Oddsson, 2013; van Waart et al., 2015), sometimes referred to as the “use it or lose it” principle (Hart, 2021). This phenomenon is problematic because individuals sometimes become sedentary due to health problems unrelated to their balance disorders. Likewise, long-term compliance with exercise interventions is a challenge, due to motivation or lack of safety resources, and has been reported to be low with over half of participants not being compliant (Sluijs et al., 1993; Alexandre et al., 2002), likely causing diminished benefits of the exercise intervention.

The improvements in clinical outcomes we report here, were gained from a single, brief training visit on the use of the sensory prosthesis and then simply by wearing it during regular daily activities. By comparison, obtaining the benefits of an exercise intervention requires the presence and engagement by the individual, at multiple therapy visits. In fact, during the first 10 weeks of use, we prohibited participants from joining in any physical therapy or balance-related exercise activities to help isolate the effect of the device (Oddsson et al., 2020). Knowing, however, that such interventions may help improve gait and balance function (Tofthagen et al., 2012), we felt it would potentially be unsafe and even unethical to prevent participation in those activities beyond the primary endpoint at 10 weeks. Therefore, to control for any potential effects of balance exercise interventions, we asked participants during follow-up phone calls at 14, 18, and 22 weeks whether they had begun any physical therapy for their balance problems. Not surprisingly, only one of the participants answered “yes” to this question, emphasizing the above-mentioned challenge with exercise engagement and compliance, and further suggesting that long-term use of the device was the main cause of improvement in clinical outcomes.

Exercise dosing vs. daily exposure from sensory prosthesis use

These improvements in clinical outcomes are not surprising, because the mechanisms for improved gait and balance function from exercise interventions are different than the mechanisms for using a sensory prosthesis to replace an important component of somatosensory balance input, in this case from plantar mechanoreceptors (Meyer et al., 2004; Fallon et al., 2005; Strzalkowski et al., 2018). Traditional balance training activities stimulate existing sensorimotor integration by challenging function with a series of successively more difficult motor tasks. This kind of treatment gradually improves performance based on important and well-known principles of training (Oddsson et al., 2007). Such improvement may be attributable to training of specific splinter skills, and some improvement may be due to compensation for balance issues from impaired plantar sensation or address other balance related impairments. Users of a sensory prosthesis, however, receive new functional sensory stimuli on a nearly continuous basis that are highly specific to standing and walking and replace their impaired sense; and these new stimuli provide sensory information that the central nervous system expects to receive from the lower extremities during such activities (Guertin, 2012, Clark, 2015).

To analyze this contrast further, a research trial of traditional balance training interventions typically provides one-hour balance stimulation sessions about 2–3 times per week for 3–6 months e.g., (Shumway-Cook et al., 1997; Wolf et al., 2001, 2003; Li et al., 2005; Li and Manor, 2010; Melzer and Oddsson, 2013; Manor et al., 2014). Assuming 100% compliance, this example would add up to an overall exercise dose of no more than 72 h of focused therapeutic balance stimulation over 6 months. In a typical therapy practice, the dose would more likely be in the range of 8–40 h, for several reasons (HS Cohen, EdD, OTR, and personal communication). Patients sometimes miss visits due to schedule conflicts. Patients may shorten the total length of treatment either because they feel they have reached their maximum level of improvement, because they dislike the hassle of taking the time for the therapy visit, or because they cannot get transportation. In addition, some insurance programs may refuse to pay for more than a limited number of therapy visits. In the case of exposure to balance stimuli from a sensory prosthesis, however, participants used the device on average 36.1 hours/week with more than 80% using the device over 21 hours/week (Oddsson et al., 2020). Over 26 weeks this use would amount to a range from around 500 to almost 1000 h of specific gait and balance stimulation, essentially an order of magnitude higher than a regular balance training intervention. Furthermore, the device is intended to be used on a continuous basis, which furthers compliance.

Participants may not be physically active and receiving sensory stimuli the entire abovementioned time. However, they will regularly experience hundreds of specific balance stimuli/hour that are intimately integrated into their regular standing and walking activities and that are likely to cause related changes in balance behavior. Over time, this feedback may lead to a reweighting of sensory information that is relevant for balance function (Sienko et al., 2018), as has previously been suggested in older adults performing in-home balance training using vibrotactile sensory stimulation related to trunk tilt (Noohi et al., 2017, Bao et al., 2018) further supported by recently reported changes in brain connectivity (Bao et al., 2022).

Interestingly, early observations from a pilot study of five participants in the cohort studied here, who completed 26 weeks of device use, show neuroplastic changes in brain network connectivity related to postural control and balance that were associated with improved changes in FGA scores (Hsu et al., 2021). This finding indicates a direct effect of the sensory prosthesis initiating plastic changes related to sensorimotor interaction and postural control. Related observations on sensorimotor neuroplastic effects associated with peripheral afferent activity have previously been made following a novel amputation strategy, agonist-antagonist myoneural interface, intended to maintain neuromuscular communication of the lost limb (Srinivasan et al., 2020). This surgical technique intends to promote proprioceptive feedback and cause central sensorimotor plastic changes that may facilitate control of a prosthetic limb (Srinivasan et al., 2020). In a similar fashion, the current non-invasive sensory prosthesis is externally providing new tactile afference, essentially through the same dermatomes that signaled plantar pressure information from mechanoreceptors that have become functionally deafferented due to PN (Fallon et al., 2005; Koehler-McNicholas et al., 2019; Vaughan, 2021).

Activities-Specific Balance Confidence to Functional Gait Assessment ratios, self-reported outcomes and device use

On the ABC, 67% is the cut-off for high-fall risk (Lajoie and Gallagher, 2004). We previously reported that participants with baseline ABC scores below 67% improved their ABC scores after 10 weeks of device use, whereas those with ABC scores above 67% did not, although both subgroups improved their FGA scores (Oddsson et al., 2020). Since these two categories of participants had similar baseline FGA scores, the discrepancy in ABC scores led to seemingly high baseline ABC to FGA ratios in participants with high ABC scores (Oddsson et al., 2020; Figure 5). We posited that the high ratio individuals were either too confident or simply unaware of their abilities or impairments, a construct that aligns with a proposed multifactorial causation model for falls emphasizing the importance of a “Realistic Appraisal of One’s Own Abilities,” (Hadjistavropoulos et al., 2011). This ratio indicates the degree of internal self-perception of balance capability (ABC score) in relation to the externally observed performance (FGA score). A ratio of around 3.3 would be “expected” based on the maximum scores of the two scales (Powell and Myers, 1995; Wrisley and Kumar, 2010). We further noted that after 6 weeks of device use, the overly confident participants appeared to “normalize” their self-perception indicating a more sensible perception of their abilities and align with those holding more expected ABC scores. This change was mainly due to an improvement in their FGA score and a maintained or slightly decreased ABC score.

We show here that this observation is preserved after 26 weeks of device use (Figure 5). This change in self confidence is important because it is a fall risk factor. As the data suggest, this ratio is a modifiable risk factor. Therefore, the ratio can and should be measured during studies of balance interventions.

Furthermore, the current data (Figure 5) shows that the high-confidence individuals appear to improve their FGA scores more than the low confidence individuals. Since the baseline FGA scores were similar for these two cohorts, it could be argued that the higher balance-confidence individuals may have “naturally” challenged themselves more in their daily activities, triggering a larger increase in FGA score. Correspondingly, the low balance-confidence individuals may have “explored” their improved functional capabilities less than the high confidence group leading to a less beneficial long-term effect. We postulate that individuals with low balance confidence would potentially benefit further from a guided interaction through physical and occupational therapy or other means, whereas the high confidence individuals may be better at “self-coaching” their renewed capabilities. Consequently, to provide an individually optimized rehabilitation strategy for falls prevention and self-efficacy, clinicians should monitor outcomes that measure both balance outcomes and balance confidence, similar to the ratio we have used to allow this construct to be investigated further (Hadjistavropoulos et al., 2011; Soh et al., 2021).

Additional observations related to self-report measures were in line with our previous reporting (Oddsson et al., 2020), overall showing marginal changes and likely being less clinically meaningful since they were near the average for the United States population (Hahn et al., 2014, 2016a,b; Askew et al., 2016). The continued high level of device use, on average more than five days a week and over 70% of participants using it every day or at least 5 days/week, suggests that users find the device helpful.

Falls data

One of the most important findings from this trial is the 43% decrease in fall rate for participants with a fall history following 26 weeks of device use. We reported an encouraging 46% decrease already after 10 weeks of use (Oddsson et al., 2020), while appreciating that 10 weeks would not be long enough for a relevant comparison to 6 months of pre-study data. Consequently, the similar statistically significant decrease after 26 weeks provides a stronger argument for a meaningful decrease in falls. In fact, even including the pre-study non-fallers in the analysis showed a statistically significant decrease in fall rate over 26 weeks of device use (Table 5). Note, however, that fall rate was not a primary outcome in this trial. In fact, we gathered pre-study falls data primarily as a means of describing our study population, and we monitored falls during the trial as a subset of adverse events. Thus, we enrolled participants at high fall risk based on their FGA scores, irrespective of whether or not they had fallen in the past. This procedure allowed us to conduct a post hoc analysis and investigate any trend in the data indicating an actual decrease in falls. A comparison with historical self-report data on prior falls is far from ideal as compared to a parallel arm trial with a control group, but other investigators have found that asking individuals to recall past falls commonly leads to an underreporting of actual falls; even recalling the past 3 months led to 25% underreporting of falls (Hannan et al., 2010), and 26% did not recall falls over the prior 6 months (Cummings et al., 1988). Under such circumstances, the 43% decrease in falls reported here probably underestimates the real effect.

The data on injuries reported from falls are probably clinically significant. Previous studies have reported that 65% of older individuals with PN fell over a year with 30% reporting an injury from a fall (DeMott et al., 2007). In a study of individuals with chemotherapy-induced PN, over 40% experienced falls, and more than 40% of falls resulted in an injury, two-thirds of which were fractures (Komatsu et al., 2019). In this study, 57% of participants reported falling in the 6 months prior to the study while 45% fell during 6 months of the trial. Eight of the 39 falls during the trial (20.5%) led to injuries where treatment was sought, half of those considered serious. Consequently, both fall rate and injury rate are lower than previous reports of similar populations (DeMott et al., 2007; Komatsu et al., 2019).

Study limitations

This study had several limitations, as we have previously outlined (Oddsson et al., 2020). It was an unblinded, single arm trial. Our decision to conduct a single arm trial was based on several factors, including previous results from an in-clinic randomized control cross-over trial showing improved FGA scores when using the device turned on compared to off (Koehler-McNicholas et al., 2019). In addition, data from the first-in-human, long-term use study showed remarkable improvements in clinical outcomes in a patient with PN using the device for a year following over 5 months of balance physical therapy with limited improvement (Wrisley et al., 2021). This individual continues to use the device daily, now for more than 4 years. Also, blinding participants in a study using this kind of intervention is challenging and may not really be viable unless some form of deception is used since a requirement to use the device is perceiving the tactile stimuli (Oddsson et al., 2020). Consequently, the most feasible placebo treatment for a control group would likely be wearing a device that is non-functional.

An important strength of the trial includes our real-life inclusion/exclusion criteria that were essentially the same as the requirements for receiving a prescription for the device outside of a research trial. These requirements are aligned with the intentions of a pragmatic clinical trial to advance applicability of study findings (Patsopoulos, 2011; Gill et al., 2021). Only 7% of participants (6 of 85) were excluded due to medical circumstances (Figure 2). We wanted the participants to realistically reflect patients who are seen in the clinic, and we did not try to screen for only those individuals who may be the best responders. In fact, our participants reported an average of 8.3 chronic conditions, had multiple fall-risk factors, and polypharmacy (mean of 8 subscription medications).

Furthermore, the long-term benefits we report here combined with the participants not receiving any useful feedback about their outcomes or systematic encouragement during their assessments and knowing that only one individual decided to participate in a balance therapy intervention, decreases the chance these effects are placebo (Finniss et al., 2010; Enck et al., 2013; Coste and Montel, 2017). A review of placebo effects in 47 randomized control trials found large effects in subjective outcomes and small effects in clinical outcomes, which is the opposite of what we report here, further suggesting effects are due to device use. Additional strengths include our use of recommended standardized objective clinical outcome measures (Moore et al., 2018) and the involvement of multiple clinical sites from different regions using different evaluators.

Conclusion

Patients with peripheral neuropathy who have gait and balance problems with a high risk of falls including a history of falls improve their walking balance and decrease their fall rates from long-term use of a wearable non-invasive sensory prosthesis.

Data availability statement

The original contributions presented in this study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving human participants were reviewed and approved by Advarra IRB (formerly Quorum Review IRB), serving as the Institutional Review Board (IRB) of record for three of the participating sites under the study protocol. The three sites include Baylor College of Medicine, Houston, TX; Hebrew SeniorLife, a Harvard Medical School Affiliate, Boston, MA; and M Health Fairview, Minneapolis, MN. The IRB Subcommittee, the Subcommittee on Research Safety, and the Research and Development Committee of the Minneapolis VA Health Care System (MVAHCS) also approved the trial. The study is registered on ClinicalTrials.gov (#NCT03538756). All necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived. The patients/participants provided their written informed consent to participate in this study.

Author contributions

LO was involved in conception, study design, data analysis, database development, and wrote the first draft of the manuscript. TB, II, and PM performed data acquisition. HC was involved in design and data analysis. LJ was involved in training and monitoring, data analysis, and drafted early sections. DK was involved in design and data acquisition. LL and BM were involved in study design. YR developed the REDCap Cloud database, training, monitoring, data analysis and drafted the early sections. DW was involved in conception, design, and outcomes standardization training. SK-M was part of conception, design, data acquisition, and analysis. All authors contributed to data interpretation, critical review and manuscript revisions, read, and approved version to be submitted.

Acknowledgments

We thank Lori Danzl, Alexandria Lloyd, and Christine Olney (Minneapolis Department of Veterans Affairs Health Care System, Minneapolis, MN, United States), Jackie Geiser, Tien Dat Nguyen, and Delorianne Sander (M Health Fairview, Minneapolis, MN, United States), Nathan Silver (Baylor College of Medicine, Houston, TX, United States), and Wanting Yu (Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Roslindale, MA, United States) for providing study coordination, participant recruitment and data gathering activities. We also thank Amy Gravely, MA, for input on statistical analysis and Annette Xenopoulos-Oddsson (University of Minnesota, Minneapolis, MN, United States), Lee Newcomer, and Steven Stern for reviewing drafts of the manuscript. The manuscript was published as a MedRxiv preprint.

Conflict of interest

LO is an inventor of the technology, Co-Founder of RxFunction Inc., a shareholder in the company, serves on its Board of Directors, and is an employee of the company. LJ and YR are employees and shareholders of RxFunction Inc.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Footnotes

  1. ^ https://www.redcapcloud.com/

References

Alexandre, N. M., Nordin, M., Hiebert, R., and Campello, M. (2002). Predictors of compliance with short-term treatment among patients with back pain. Rev. Panam. Salud. Publica. 12, 86–94. doi: 10.1590/S1020-49892002000800003

PubMed Abstract | CrossRef Full Text | Google Scholar

Algina, J., Keselman, H. J., and Penfield, R. D. (2005). Effect sizes and their intervals: The two-level repeated measures case. Educ. Psychol. Meas. 65, 241–258. doi: 10.1177/0013164404268675

CrossRef Full Text | Google Scholar

Askew, R. L., Cook, K. F., Revicki, D. A., Cella, D., and Amtmann, D. (2016). Evidence from diverse clinical populations supported clinical validity of PROMIS pain interference and pain behavior. J. Clin. Epidemiol. 73, 103–111. doi: 10.1016/j.jclinepi.2015.08.035

PubMed Abstract | CrossRef Full Text | Google Scholar

Bao, T., Carender, W. J., Kinnaird, C., Barone, V. J., Peethambaran, G., Whitney, S. L., et al. (2018). Effects of long-term balance training with vibrotactile sensory augmentation among community-dwelling healthy older adults: A randomized preliminary study. J. Neuroeng. Rehabil. 15:5. doi: 10.1186/s12984-017-0339-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Bao, T., Noohi, F., Kinnaird, C., Carender, W. J., Barone, V. J., Peethambaran, G., et al. (2022). Retention effects of long-term balance training with vibrotactile sensory augmentation in healthy older adults. Sensors (Basel) 22:3014. doi: 10.3390/s22083014

PubMed Abstract | CrossRef Full Text | Google Scholar

Beninato, M., Fernandes, A., and Plummer, L. S. (2014). Minimal clinically important difference of the functional gait assessment in older adults. Phys. Ther. 94, 1594–1603. doi: 10.2522/ptj.20130596

PubMed Abstract | CrossRef Full Text | Google Scholar

Bergen, G., Stevens, M. R., and Burns, E. R. (2016). Falls and fall injuries among adults aged = 65 years–United States, 2014. MMWR Morb. Mortal Wkly. Rep. 65, 993–998. doi: 10.15585/mmwr.mm6537a2

PubMed Abstract | CrossRef Full Text | Google Scholar

Buracchio, T., Dodge, H. H., Howieson, D., Wasserman, D., and Kaye, J. (2010). The trajectory of gait speed preceding mild cognitive impairment. Arch. Neurol. 67, 980–986. doi: 10.1001/archneurol.2010.159

PubMed Abstract | CrossRef Full Text | Google Scholar

Cavanagh, P. R., Derr, J. A., Ulbrecht, J. S., Maser, R. E., and Orchard, T. J. (1992). Problems with gait and posture in neuropathic patients with insulin-dependent diabetes mellitus. Diabet. Med. 9, 469–474. doi: 10.1111/j.1464-5491.1992.tb01819.x

PubMed Abstract | CrossRef Full Text | Google Scholar

CDC (2017). STEADI–older adult fall prevention. Available online at: https://www.cdc.gov/steadi/materials.html (accessed May 5, 2018)

Google Scholar

CDC (2021). Older adult fall prevention. Available online at: https://www.cdc.gov/falls/facts.html (accessed November 1, 2021)

Google Scholar

Cesari, M., Kritchevsky, S. B., Penninx, B. W., Nicklas, B. J., Simonsick, E. M., Newman, A. B., et al. (2005). Prognostic value of usual gait speed in well-functioning older people–results from the health, aging and body composition study. J. Am. Geriatr. Soc. 53, 1675–1680. doi: 10.1111/j.1532-5415.2005.53501.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Clark, D. J. (2015). Automaticity of walking: Functional significance, mechanisms, measurement and rehabilitation strategies. Front. Hum. Neurosci. 9:246. doi: 10.3389/fnhum.2015.00246

PubMed Abstract | CrossRef Full Text | Google Scholar

Clark, D. J., Christou, E. A., Ring, S. A., Williamson, J. B., and Doty, L. (2014). Enhanced somatosensory feedback reduces prefrontal cortical activity during walking in older adults. J. Gerontol. A Biol. Sci. Med. Sci. 69, 1422–1428. doi: 10.1093/gerona/glu125

PubMed Abstract | CrossRef Full Text | Google Scholar

Cohen, H. S., Kimball, K. T., and Adams, A. S. (2000). Application of the vestibular disorders activities of daily living scale. Laryngoscope 110, 1204–1209. doi: 10.1097/00005537-200007000-00026

PubMed Abstract | CrossRef Full Text | Google Scholar

Cohen, J. (1988). Statistical power analysis for the behavioral sciences. New York, NY: Routledge Academic.

Google Scholar

Cohen, M. A., Miller, J., Shi, X., Sandhu, J., and Lipsitz, L. A. (2015). Prevention program lowered the risk of falls and decreased claims for long-term services among elder participants. Health Aff. (Millwood) 34, 971–977. doi: 10.1377/hlthaff.2014.1172

PubMed Abstract | CrossRef Full Text | Google Scholar

Coste, J., and Montel, S. (2017). Placebo-related effects: A meta-narrative review of conceptualization, mechanisms and their relevance in rheumatology. Rheumatology (Oxford) 56, 334–343. doi: 10.1093/rheumatology/kew274

PubMed Abstract | CrossRef Full Text | Google Scholar

Cummings, S. R., Nevitt, M. C., and Kidd, S. (1988). Forgetting falls. The limited accuracy of recall of falls in the elderly. J. Am. Geriatr. Soc. 36, 613–616. doi: 10.1111/j.1532-5415.1988.tb06155.x

PubMed Abstract | CrossRef Full Text | Google Scholar

DeMott, T. K., Richardson, J. K., Thies, S. B., and Ashton-Miller, J. A. (2007). Falls and gait characteristics among older persons with peripheral neuropathy. Am J Phys Med Rehabil 86, 125–132. doi: 10.1097/PHM.0b013e31802ee1d1

PubMed Abstract | CrossRef Full Text | Google Scholar

Dixon, C. J., Knight, T., Binns, E., Ihaka, B., and O’Brien, D. (2017). Clinical measures of balance in people with type two diabetes: A systematic literature review. Gait Posture 58, 325–332. doi: 10.1016/j.gaitpost.2017.08.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Dumurgier, J., Elbaz, A., Ducimetière, P., Tavernier, B., Alpérovitch, A., and Tzourio, C. (2009). Slow walking speed and cardiovascular death in well functioning older adults: Prospective cohort study. BMJ 339:b4460. doi: 10.1136/bmj.b4460

PubMed Abstract | CrossRef Full Text | Google Scholar

Enck, P., Bingel, U., Schedlowski, M., and Rief, W. (2013). The placebo response in medicine: Minimize, maximize or personalize? Nat. Rev. Drug Discov. 12, 191–204. doi: 10.1038/nrd3923

PubMed Abstract | CrossRef Full Text | Google Scholar

Fallon, J. B., Bent, L. R., McNulty, P. A., and Macefield, V. G. (2005). Evidence for strong synaptic coupling between single tactile afferents from the sole of the foot and motoneurons supplying leg muscles. J. Neurophysiol. 94, 3795–3804. doi: 10.1152/jn.00359.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

Finniss, D. G., Kaptchuk, T. J., Miller, F., and Benedetti, F. (2010). Biological, clinical, and ethical advances of placebo effects. Lancet 375, 686–695. doi: 10.1016/S0140-6736(09)61706-2

CrossRef Full Text | Google Scholar

Ganz, D. A., and Latham, N. K. (2020). Prevention of falls in community-dwelling older adults. N. Engl. J. Med. 382, 734–743. doi: 10.1056/NEJMcp1903252

PubMed Abstract | CrossRef Full Text | Google Scholar

Gill, T. M., Bhasin, S., Reuben, D. B., Latham, N. K., Araujo, K., Ganz, D. A., et al. (2021). Effect of a multifactorial fall injury prevention intervention on patient well-being: The STRIDE Study. J. Am. Geriatr. Soc. 69, 173–179. doi: 10.1111/jgs.16854

PubMed Abstract | CrossRef Full Text | Google Scholar

Gregg, E. W., Sorlie, P., Paulose-Ram, R., Gu, Q., Eberhardt, M. S., Wolz, M., et al. (2004). Prevalence of lower-extremity disease in the US adult population >=40 years of age with and without diabetes: 1999-2000 national health and nutrition examination survey. Diabet. Care 27, 1591–1597. doi: 10.2337/diacare.27.7.1591

PubMed Abstract | CrossRef Full Text | Google Scholar

Guertin, P. A. (2012). Central pattern generator for locomotion: Anatomical, physiological, and pathophysiological considerations. Front. Neurol. 3:183. doi: 10.3389/fneur.2012.00183

PubMed Abstract | CrossRef Full Text | Google Scholar

Hadjistavropoulos, T., Delbaere, K., and Fitzgerald, T. D. (2011). Reconceptualizing the role of fear of falling and balance confidence in fall risk. J. Aging Health 23, 3–23. doi: 10.1177/0898264310378039

PubMed Abstract | CrossRef Full Text | Google Scholar

Hahn, E. A., DeWalt, D. A., Bode, R. K., Garcia, S. F., DeVellis, R. F., Correia, H., et al. (2014). New english and spanish social health measures will facilitate evaluating health determinants. Health Psychol. 33, 490–499. doi: 10.1037/hea0000055

PubMed Abstract | CrossRef Full Text | Google Scholar

Hahn, E. A., Kallen, M. A., Jensen, R. E., Potosky, A. L., Moinpour, C. M., Ramirez, M., et al. (2016b). Measuring social function in diverse cancer populations: Evaluation of measurement equivalence of the patient reported outcomes measurement information system. Psychol. Test Assess. Model 58, 403–421.

Google Scholar

Hahn, E. A., Beaumont, J. L., Pilkonis, P. A., Garcia, S. F., Magasi, S., DeWalt, D. A., et al. (2016a). The PROMIS satisfaction with social participation measures demonstrated responsiveness in diverse clinical populations. J. Clin. Epidemiol. 73, 135–141. doi: 10.1016/j.jclinepi.2015.08.034

PubMed Abstract | CrossRef Full Text | Google Scholar

Halvarsson, A., Franzén, E., Farén, E., Olsson, E., Oddsson, L., and Ståhle, A. (2013). Long-term effects of new progressive group balance training for elderly people with increased risk of falling–a randomized controlled trial. Clin. Rehabil. 27, 450–458. doi: 10.1177/0269215512462908

PubMed Abstract | CrossRef Full Text | Google Scholar

Hanewinckel, R., Drenthen, J., Verlinden, V. J. A., Darweesh, S. K. L., van der Geest, J. N., Hofman, A., et al. (2017). Polyneuropathy relates to impairment in daily activities, worse gait, and fall-related injuries. Neurology 89, 76–83. doi: 10.1212/WNL.0000000000004067

PubMed Abstract | CrossRef Full Text | Google Scholar

Hannan, M. T., Gagnon, M. M., Aneja, J., Jones, R. N., Cupples, L. A., Lipsitz, L. A., et al. (2010). Optimizing the tracking of falls in studies of older participants: Comparison of quarterly telephone recall with monthly falls calendars in the MOBILIZE Boston Study. Am. J. Epidemiol. 171, 1031–1036. doi: 10.1093/aje/kwq024

PubMed Abstract | CrossRef Full Text | Google Scholar

Hardy, S. E., Perera, S., Roumani, Y. F., Chandler, J. M., and Studenski, S. A. (2007). Improvement in usual gait speed predicts better survival in older adults. J. Am. Geriatr. Soc. 55, 1727–1734. doi: 10.1111/j.1532-5415.2007.01413.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hart, D. A. (2021). “Learning from human responses to deconditioning environments: Improved understanding of the “Use It or Lose It” principle. Front. Sports Act Living 3:685845. doi: 10.3389/fspor.2021.685845

PubMed Abstract | CrossRef Full Text | Google Scholar

Hicks, C. W., Wang, D., Windham, B. G., Matsushita, K., and Selvin, E. (2021). Prevalence of peripheral neuropathy defined by monofilament insensitivity in middle-aged and older adults in two US cohorts. Sci. Rep. 11:19159. doi: 10.1038/s41598-021-98565-w

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoffman, E. M., Staff, N. P., Robb, J. M., St Sauver, J. L., Dyck, P. J., and Klein, C. J. (2015). Impairments and comorbidities of polyneuropathy revealed by population-based analyses. Neurology 84, 1644–1651. doi: 10.1212/WNL.0000000000001492

PubMed Abstract | CrossRef Full Text | Google Scholar

Hsu, C. L., Iloputaife, I., Oddsson, L., Manor, B., and Lipsitz, L. (2021). Six-Month lower-leg sensory stimulation augments neural network connectivity associated with improved gait. Innovation in aging 5(Suppl. 1), 960–961. doi: 10.1093/geroni/igab046.3439

CrossRef Full Text | Google Scholar

Ites, K. I., Anderson, E. J., Cahill, M. L., Kearney, J. A., Post, E. C., and Gilchrist, L. S. (2011). Balance interventions for diabetic peripheral neuropathy: A systematic review. J. Geriatr. Phys. Ther. 34, 109–116. doi: 10.1519/JPT.0b013e318212659a

PubMed Abstract | CrossRef Full Text | Google Scholar

Kästenbauer, T., Sauseng, S., Brath, H., Abrahamian, H., and Irsigler, K. (2004). The value of the Rydel-Seiffer tuning fork as a predictor of diabetic polyneuropathy compared with a neurothesiometer. Diabet. Med. 21, 563–567. doi: 10.1111/j.1464-5491.2004.01205.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, D. H., Glynn, R. J., Avorn, J., Lipsitz, L. A., Rockwood, K., Pawar, A., et al. (2019). Validation of a claims-based frailty index against physical performance and adverse health outcomes in the health and retirement study. J. Gerontol. A Biol. Sci. Med. Sci. 74, 1271–1276. doi: 10.1093/gerona/gly197

PubMed Abstract | CrossRef Full Text | Google Scholar

Koehler-McNicholas, S. R., Danzl, L., Cataldo, A. Y., and Oddsson, L. I. E. (2019). Neuromodulation to improve gait and balance function using a sensory neuroprosthesis in people who report insensate feet–A randomized control cross-over study. PLoS One 14:e0216212. doi: 10.1371/journal.pone.0216212

PubMed Abstract | CrossRef Full Text | Google Scholar

Komatsu, H., Yagasaki, K., Komatsu, Y., Yamauchi, H., Yamauchi, T., Shimokawa, T., et al. (2019). Falls and functional impairments in breast cancer patients with chemotherapy-induced peripheral neuropathy. Asia Pac. J. Oncol. Nurs. 6, 253–260. doi: 10.4103/apjon.apjon_7_19

CrossRef Full Text | Google Scholar

Koski, K., Luukinen, H., Laippala, P., and Kivelä, S. L. (1998). Risk factors for major injurious falls among the home-dwelling elderly by functional abilities. A prospective population-based study. Gerontology 44, 232–238. doi: 10.1159/000022017

PubMed Abstract | CrossRef Full Text | Google Scholar

Kroenke, K., Spitzer, R. L., and Williams, J. B. (2001). The PHQ-9: Validity of a brief depression severity measure. J. Gen. Intern. Med. 16, 606–613. doi: 10.1046/j.1525-1497.2001.016009606.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kruse, R. L., Lemaster, J. W., and Madsen, R. W. (2010). Fall and balance outcomes after an intervention to promote leg strength, balance, and walking in people with diabetic peripheral neuropathy: “Feet first” randomized controlled trial. Phys. Ther. 90, 1568–1579. doi: 10.2522/ptj.20090362

PubMed Abstract | CrossRef Full Text | Google Scholar

Lajoie, Y., and Gallagher, S. P. (2004). Predicting falls within the elderly community: Comparison of postural sway, reaction time, the Berg balance scale and the Activities-specific Balance Confidence (ABC) scale for comparing fallers and non-fallers. Arch. Gerontol. Geriatr. 38, 11–26. doi: 10.1016/S0167-4943(03)00082-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Lakens, D. (2013). Calculating and reporting effect sizes to facilitate cumulative science: A practical primer for t-tests and ANOVAs. Front. Psychol. 4:863. doi: 10.3389/fpsyg.2013.00863

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, F., Harmer, P., Fisher, K. J., McAuley, E., Chaumeton, N., Eckstrom, E., et al. (2005). Tai Chi and fall reductions in older adults: A randomized controlled trial. J. Gerontol. A Biol. Sci. Med. Sci. 60, 187–194. doi: 10.1093/gerona/60.2.187

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, L., and Manor, B. (2010). Long term Tai Chi exercise improves physical performance among people with peripheral neuropathy. Am. J. Chin. Med. 38, 449–459. doi: 10.1142/S0192415X1000797X

PubMed Abstract | CrossRef Full Text | Google Scholar

Lipsitz, L. A., Macklin, E. A., Travison, T. G., Manor, B., Gagnon, P., Tsai, T. I, et al. (2019). A cluster randomized trial of Tai Chi vs health education in subsidized housing: The MI-WiSH study. J. Am. Geriatr. Soc. 67, 1812–1819. doi: 10.1111/jgs.15986

PubMed Abstract | CrossRef Full Text | Google Scholar

Lipsitz, L. A., Manor, B., Habtemariam, D., Iloputaife, I., Zhou, J., and Travison, T. G. (2018). The pace and prognosis of peripheral sensory loss in advanced age: Association with gait speed and falls. BMC Geriatr. 18:274. doi: 10.1186/s12877-018-0970-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Manor, B., Lough, M., Gagnon, M. M., Cupples, A., Wayne, P. M., and Lipsitz, L. A. (2014). Functional benefits of tai chi training in senior housing facilities. J. Am. Geriatr. Soc. 62, 1484–1489. doi: 10.1111/jgs.12946

PubMed Abstract | CrossRef Full Text | Google Scholar

Mathias, S., Nayak, U. S., and Isaacs, B. (1986). Balance in elderly patients: The “get-up and go” test. Arch. Phys. Med. Rehabil. 67, 387–389.

PubMed Abstract | Google Scholar

Melzer, I., and Oddsson, LIe (2013). Improving balance control and self-reported lower extremity function in community-dwelling older adults: A randomized control trial. Clin. Rehabil. 27, 195–206. doi: 10.1177/0269215512450295

PubMed Abstract | CrossRef Full Text | Google Scholar

Menz, H. B., Lord, S. R., St George, R., and Fitzpatrick, R. C. (2004). Walking stability and sensorimotor function in older people with diabetic peripheral neuropathy. Arch. Phys. Med. Rehabil. 85, 245–252. doi: 10.1016/j.apmr.2003.06.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyer, P. F., Oddsson, L. I., and De Luca, C. J. (2004a). Reduced plantar sensitivity alters postural responses to lateral perturbations of balance. Exp. Brain Res. 157, 526–536. doi: 10.1007/s00221-004-1868-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyer, P. F., Oddsson, L. I., and De Luca, C. J. (2004b). The role of plantar cutaneous sensation in unperturbed stance. Exp. Brain Res. 156, 505–512. doi: 10.1007/s00221-003-1804-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Montero-Odasso, M. M., Kamkar, N., Pieruccini-Faria, F., Osman, A., Sarquis-Adamson, Y., Close, J., et al. (2021). Evaluation of clinical practice guidelines on fall prevention and management for older adults: A systematic review. JAMA Netw. Open 4:e2138911.

Google Scholar

Montero-Odasso, M., Schapira, M., Soriano, E. R., Varela, M., Kaplan, R., Camera, L. A., et al. (2005). Gait velocity as a single predictor of adverse events in healthy seniors aged 75 years and older. J. Gerontol. A Biol. Sci. Med. Sci. 60, 1304–1309. doi: 10.1093/gerona/60.10.1304

PubMed Abstract | CrossRef Full Text | Google Scholar

Moore, J. L., Potter, K., Blankshain, K., Kaplan, S. L., O’Dwyer, L. C., and Sullivan, J. E. (2018). A core set of outcome measures for adults with neurologic conditions undergoing rehabilitation: A Clinical Practice Guideline. J. Neurol. Phys. Ther. 42, 174–220. doi: 10.1097/NPT.0000000000000229

PubMed Abstract | CrossRef Full Text | Google Scholar

Moreland, B., Kakara, R., and Henry, A. (2020). Trends in nonfatal falls and fall-related injuries among adults aged = 65 years–United States, 2012-2018. MMWR Morb. Mortal Wkly. Rep. 69, 875–881. doi: 10.15585/mmwr.mm6927a5

PubMed Abstract | CrossRef Full Text | Google Scholar

Morris, S. B., and DeShon, R. P. (2002). Combining effect size estimates in meta-analysis with repeated measures and independent-groups designs. Psychol. Methods 7, 105–125. doi: 10.1037/1082-989X.7.1.105

PubMed Abstract | CrossRef Full Text | Google Scholar

Morrison, S., Simmons, R., Colberg, S. R., Parson, H. K., and Vinik, A. I. (2018). Supervised balance training and wii fit-based exercises lower falls risk in older adults with type 2 diabetes. J. Am. Med. Dir. Assoc. 19, .e187–.e185. doi: 10.1016/j.jamda.2017.11.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Mustapa, A., Justine, M., Mohd Mustafah, N., Jamil, N., and Manaf, H. (2016). Postural control and gait performance in the diabetic peripheral neuropathy: A systematic review. Biomed. Res. Int. 2016:9305025. doi: 10.1155/2016/9305025

PubMed Abstract | CrossRef Full Text | Google Scholar

Noohi, F., Kinnaird, C., DeDios, Y. I, Kofman, S., Wood, S., Bloomberg, J., et al. (2017). Functional brain activation in response to a clinical vestibular test correlates with balance. Front. Syst. Neurosci. 11:11. doi: 10.3389/fnsys.2017.00011

PubMed Abstract | CrossRef Full Text | Google Scholar

Oddsson, L. I. E., Bisson, T., Cohen, H. S., Jacobs, L., Khoshnoodi, M., Kung, D., et al. (2020). The effects of a wearable sensory prosthesis on gait and balance function after 10 weeks of use in persons with peripheral neuropathy and high fall risk–The walk2Wellness trial. Front. Aging Neurosci. 12:592751. doi: 10.3389/fnagi.2020.592751

PubMed Abstract | CrossRef Full Text | Google Scholar

Oddsson, L. I. E., Boissy, P., and Melzer, I. (2007). How to improve gait and balance function in elderly individuals—compliance with principles of training. Eur. Rev. Aging Phys. Act 4, 15–23. doi: 10.1007/s11556-007-0019-9

CrossRef Full Text | Google Scholar

Patsopoulos, N. A. (2011). A pragmatic view on pragmatic trials. Dialogues Clin. Neurosci. 13, 217–224. doi: 10.31887/DCNS.2011.13.2/npatsopoulos

CrossRef Full Text | Google Scholar

Paul, S. S., Ada, L., and Canning, C. G. (2005). Automaticity of walking–implications for physiotherapy practice. Phys. Ther. Rev. 10, 15–23. doi: 10.1179/108331905X43463

CrossRef Full Text | Google Scholar

Perera, S., Mody, S. H., Woodman, R. C., and Studenski, S. A. (2006). Meaningful change and responsiveness in common physical performance measures in older adults. J. Am. Geriatr. Soc. 54, 743–749. doi: 10.1111/j.1532-5415.2006.00701.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Powell, L. E., and Myers, A. M. (1995). The activities-specific balance confidence (ABC) scale. J. Gerontol. A Biol. Sci. Med. Sci. 50A, M28–M34. doi: 10.1093/gerona/50A.1.M28

PubMed Abstract | CrossRef Full Text | Google Scholar

Quigley, P. A., Bulat, T., Schulz, B., Friedman, Y., Hart-Hughes, S., Richardson, J. K., et al. (2014). Exercise interventions, gait, and balance in older subjects with distal symmetric polyneuropathy: A three-group randomized clinical trial. Am. J. Phys. Med. Rehabil. 93, 1–12. doi: 10.1097/PHM.0000000000000052

PubMed Abstract | CrossRef Full Text | Google Scholar

Reeves, N. D., Orlando, G., and Brown, S. J. (2021). Sensory-motor mechanisms increasing falls risk in diabetic peripheral neuropathy. Medicina (Kaunas) 57:457. doi: 10.3390/medicina57050457

PubMed Abstract | CrossRef Full Text | Google Scholar

Richardson, J. K., and Hurvitz, E. A. (1995). Peripheral neuropathy: A true risk factor for falls. J. Gerontol. A Biol. Sci. Med. Sci. 50, M211–M215. doi: 10.1093/gerona/50A.4.M211

PubMed Abstract | CrossRef Full Text | Google Scholar

Richardson, J. K., Sandman, D., and Vela, S. (2001). A focused exercise regimen improves clinical measures of balance in patients with peripheral neuropathy. Arch. Phys. Med. Rehabil. 82, 205–209. doi: 10.1053/apmr.2001.19742

PubMed Abstract | CrossRef Full Text | Google Scholar

Riskowski, J. L., Quach, L., Manor, B., Menz, H. B., Lipsitz, L. A., and Hannan, M. T. (2012). Idiopathic peripheral neuropathy increases fall risk in a population-based cohort study of older adults. J. Foot Ankle Res. 5:19. doi: 10.1186/1757-1146-5-S1-P19

CrossRef Full Text | Google Scholar

Sheldon, J. H. (1948). Some aspects of old age. Lancet 1, 621–624. doi: 10.1016/S0140-6736(48)90811-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Shumway-Cook, A., Gruber, W., Baldwin, M., and Liao, S. (1997). The effect of multidimensional exercises on balance, mobility, and fall risk in community-dwelling older adults. Phys. Ther. 77, 46–57. doi: 10.1093/ptj/77.1.46

PubMed Abstract | CrossRef Full Text | Google Scholar

Sienko, K. H., Seidler, R. D., Carender, W. J., Goodworth, A. D., Whitney, S. L., and Peterka, R. J. (2018). Potential mechanisms of sensory augmentation systems on human balance control. Front. Neurol. 9:944. doi: 10.3389/fneur.2018.00944

PubMed Abstract | CrossRef Full Text | Google Scholar

Sluijs, E. M., Kok, G. J., and van der Zee, J. (1993). Correlates of exercise compliance in physical therapy. Phys. Ther. 73, 771–782. doi: 10.1093/ptj/73.11.771

PubMed Abstract | CrossRef Full Text | Google Scholar

Soh, S. L., Tan, C. W., Thomas, J. I., Tan, G., Xu, T., Ng, Y. L., et al. (2021). Falls efficacy: Extending the understanding of self-efficacy in older adults towards managing falls. J. Frailty Sarcopenia Falls 6, 131–138. doi: 10.22540/JFSF-06-131

PubMed Abstract | CrossRef Full Text | Google Scholar

Srinivasan, S. S., Tuckute, G., Zou, J., Gutierrez-Arango, S., Song, H., Barry, R. L., et al. (2020). Agonist-antagonist myoneural interface amputation preserves proprioceptive sensorimotor neurophysiology in lower limbs. Sci. Transl. Med. 12:eabc592. doi: 10.1126/scitranslmed.abc5926

PubMed Abstract | CrossRef Full Text | Google Scholar

STEADI, C. (2021). STEADI—Older Adult Fall Prevention. Available online at: https://www.cdc.gov/steadi/ (accessedDecember 10, 2021)

Google Scholar

Stevens, J. A., and Phelan, E. A. (2013). Development of STEADI: A fall prevention resource for health care providers. Health Promot. Pract. 14, 706–714. doi: 10.1177/1524839912463576

PubMed Abstract | CrossRef Full Text | Google Scholar

Streckmann, F., Zopf, E. M., Lehmann, H. C., May, K., Rizza, J., Zimmer, P., et al. (2014). Exercise intervention studies in patients with peripheral neuropathy: A systematic review. Sports Med 44, 1289–1304. doi: 10.1007/s40279-014-0207-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Strzalkowski, N. D. J., Peters, R. M., Inglis, J. T., and Bent, L. R. (2018). Cutaneous afferent innervation of the human foot sole: What can we learn from single-unit recordings? J. Neurophysiol. 120, 1233–1246. doi: 10.1152/jn.00848.2017

PubMed Abstract | CrossRef Full Text | Google Scholar

Studenski, S., Perera, S., Patel, K., Rosano, C., Faulkner, K., Inzitari, M., et al. (2011). Gait speed and survival in older adults. JAMA 305, 50–58. doi: 10.1001/jama.2010.1923

PubMed Abstract | CrossRef Full Text | Google Scholar

Studenski, S., Perera, S., Wallace, D., Chandler, J. M., Duncan, P. W., Rooney, E., et al. (2003). Physical performance measures in the clinical setting. J. Am. Geriatr. Soc. 51, 314–322. doi: 10.1046/j.1532-5415.2003.51104.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Tinetti, M. E., and Kumar, C. (2010). The patient who falls: “It’s always a trade-off”. JAMA 303, 258–266. doi: 10.1001/jama.2009.2024

PubMed Abstract | CrossRef Full Text | Google Scholar

Tofthagen, C., Visovsky, C., and Berry, D. L. (2012). Strength and balance training for adults with peripheral neuropathy and high risk of fall: Current evidence and implications for future research. Oncol. Nurs. Forum 39, E416–E424. doi: 10.1188/12.ONF.E416-E424

CrossRef Full Text | Google Scholar

Uitenbroek, D. G. (1997). SISA-Binomial. Available online at: https://www.quantitativeskills.com/sisa/calculations/bonfer.htm (accessed May, 2020)

Google Scholar

van Waart, H., Stuiver, M. M., van Harten, W. H., Geleijn, E., Kieffer, J. M., Buffart, L. M., et al. (2015). Effect of low-intensity physical activity and moderate- to high-intensity physical exercise during adjuvant chemotherapy on physical fitness, fatigue, and chemotherapy completion rates: Results of the paces randomized clinical trial. J. Clin. Oncol. 33, 1918–1927. doi: 10.1200/JCO.2014.59.1081

PubMed Abstract | CrossRef Full Text | Google Scholar

Vaughan, G. M. (2021). The roles of mechanoreceptors in muscle and skin in human proprioception. Curr. Opin. Physiol. 21, 48–56. doi: 10.1016/j.cophys.2021.03.003

CrossRef Full Text | Google Scholar

Vinik, A. I., Camacho, P., Reddy, S., Valencia, W. M., Trence, D., Matsumoto, A. M., et al. (2017). Aging, Diabetes, And Falls. Endocr. Pract. 23, 1117–1139. doi: 10.4158/EP171794.RA

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, C., Goel, R., Zhang, Q., Lepow, B., and Najafi, B. (2019). Daily use of bilateral custom-made ankle-foot orthoses for fall prevention in older adults: A randomized controlled trial. J. Am. Geriatr. Soc. 67, 1656–1661. doi: 10.1111/jgs.15929

PubMed Abstract | CrossRef Full Text | Google Scholar

Winters-Stone, K. M., Horak, F., Jacobs, P. G., Trubowitz, P., Dieckmann, N. F., Stoyles, S., et al. (2017). Falls, functioning, and disability among women with persistent symptoms of chemotherapy-induced peripheral neuropathy. J. Clin. Oncol. 35, 2604–2612. doi: 10.1200/JCO.2016.71.3552

PubMed Abstract | CrossRef Full Text | Google Scholar

Wolf, B., Feys, H., De Weerdt, J., van, der Meer, Noom, M., and Aufdemkampe, G. (2001). Effect of a physical therapeutic intervention for balance problems in the elderly: A single-blind, randomized, controlled multicentre trial. Clin. Rehabil. 15, 624–636. doi: 10.1191/0269215501cr456oa

PubMed Abstract | CrossRef Full Text | Google Scholar

Wolf, S. L., Sattin, R. W., Kutner, M., O’Grady, M., Greenspan, A. I., and Gregor, R. J. (2003). Intense tai chi exercise training and fall occurrences in older, transitionally frail adults: A randomized, controlled trial. J. Am. Geriatr. Soc. 51, 1693–1701. doi: 10.1046/j.1532-5415.2003.51552.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Wrisley, D. M., and Kumar, N. A. (2010). Functional gait assessment: Concurrent, discriminative, and predictive validity in community-dwelling older adults. Phys. Ther. 90, 761–773. doi: 10.2522/ptj.20090069

PubMed Abstract | CrossRef Full Text | Google Scholar

Wrisley, D. M., Marchetti, G. F., Kuharsky, D. K., and Whitney, S. L. (2004). Reliability, internal consistency, and validity of data obtained with the functional gait assessment. Phys. Ther. 84, 906–918. doi: 10.1093/ptj/84.10.906

CrossRef Full Text | Google Scholar

Wrisley, D. M., McLean, G., Hill, J. B., and Oddsson, L. I. E. (2021). Long-term use of a sensory prosthesis improves function in a patient with peripheral neuropathy: A case report. Front. Neurol. 12:655963. doi: 10.3389/fneur.2021.655963

PubMed Abstract | CrossRef Full Text | Google Scholar

Zaiontz, C. (2020). Real statistics resource pack (Release 6.8). Available online at: http://www.real-statistics.com/ (accessed August 2021).

Google Scholar

Keywords: peripheral neuropathy, falls, balance, gait speed, neuromodulation, clinical trial, sensory prosthesis, wearable

Citation: Oddsson LIE, Bisson T, Cohen HS, Iloputaife I, Jacobs L, Kung D, Lipsitz LA, Manor B, McCracken P, Rumsey Y, Wrisley DM and Koehler-McNicholas SR (2022) Extended effects of a wearable sensory prosthesis on gait, balance function and falls after 26 weeks of use in persons with peripheral neuropathy and high fall risk—The walk2Wellness trial. Front. Aging Neurosci. 14:931048. doi: 10.3389/fnagi.2022.931048

Received: 28 April 2022; Accepted: 23 August 2022;
Published: 20 September 2022.

Edited by:

Robert Petersen, Central Michigan University, United States

Reviewed by:

Robert LeMoyne, Northern Arizona University, United States
Benjamin Walter, Cleveland Clinic, United States

Copyright © 2022 Oddsson, Bisson, Cohen, Iloputaife, Jacobs, Kung, Lipsitz, Manor, McCracken, Rumsey, Wrisley and Koehler-McNicholas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lars I. E. Oddsson, loddsson@umn.edu

Download