SYSTEMATIC REVIEW article

Front. Psychiatry, 14 April 2025

Sec. Public Mental Health

Volume 16 - 2025 | https://doi.org/10.3389/fpsyt.2025.1569709

Are mind-body therapies beneficial for older people with dementia? A Systematic Review and meta-analysis of randomized controlled trials

  • 1. School of Physical Education, Southwest University, Chongqing, China

  • 2. School of Physical Education, Shanghai University of Sport, Shanghai, China

  • 3. Faculty of Education, Southwest University, Chongqing, China

  • 4. Key Laboratory of Cognition and Personality, Faculty of Psychology, Ministry of Education, Southwest University, Chongqing, China

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Abstract

Objective:

This systematic review and meta-analysis aimed to evaluate the potential multidomain benefits of mind-body therapies (MBTs) for behavioral and psychological symptoms of dementia (BPSD) in older people with dementia (OPWD).

Methods:

Relevant randomized controlled trials (RCTs) were identified using electronic databases and manual searches. Two independent researchers evaluated the risk of bias in the included trials using the Revised Cochrane Risk-of-Bias tool for randomized trials. A standardized mean difference (SMD) with a 95% confidence interval (CI) was used to combine effect sizes.

Results:

This review included 35 RCTs comprising 4,043 patients, of whom 24 were included in the meta-analyses. MBTs effectively improved BPSD (SMD = -0.33; 95% CI -0.49 to -0.16; p < 0.01), anxiety (SMD = -0.82; 95% CI -1.53 to -0.10; p = 0.02), and depression (SMD = -0.57; 95% CI -1.06 to -0.08; p = 0.02), with no significant improvements observed in agitation (SMD = -0.09; 95% CI -0.25 to 0.07; p = 0.27) among patients with dementia. The certainty of evidence across the outcomes ranged from low to very low, based on the Grading of Recommendations, Assessment, Development, and Evaluations ratings.

Conclusion:

Effective nursing for patients with dementia is vital, as they are undergoing a major transition in their physical and mental health. In clinical practice, healthcare and social care therapists should develop personalized intervention programs based on patient individual differences and the actual dose-response relationship, which will help maximize the clinical benefits of non-pharmacological treatments in the context of limited medical resources. More high-quality RCTs could be conducted to compare the differential efficacy of non-pharmacological treatments on various aspects of BPSD in OPWD to provide a better evidence base to guide individual care and policy guidance.

Systematic review registration:

PROSPERO, identifier CRD42024559809.

1 Introduction

Dementia is a progressive cognitive disorder that impairs daily functioning and is a primary contributor to dependency, disability, and death (1, 2). It is characterized by cognitive decline, deteriorating functional status, and worsening of neuropsychiatric symptoms (3). Currently, over 50 million individuals worldwide are affected by dementia, and projections indicate this figure could rise to 131 million by 2050 (3, 4). Moreover, the overall prevalence of dementia, from all causes, stands at 7.0%, with its rate of occurrence increasing sharply with age for both men and women (5), suggesting the growing public health challenge posed by dementia as the global population continues to age.

Old age is not only a critical stage for changes in physical and mental health but also a vulnerable period for the development of dementia. During this period, older people are often exposed to multiple risk factors for developing dementia, which are classified as immutable (age, sex, ethnicity, etc.) or potentially modifiable (diabetes, smoking, social isolation, physical inactivity, etc.) (6, 7). Moreover, compelling evidence suggests that dementia is prevalent among older people and may increase their susceptibility to physical and mental health problems, including cognitive impairment (8), suicidal behavior (9), epilepsy (10), disability (11), anxiety (12), and depression (13).

Dementia can be diagnosed based on medical history, cognitive and physical examination, laboratory testing, and brain imaging (3). As dementia is a progressive, incurable illness, several medications have been developed to help older people with dementia (OPWD) alleviate the physical and mental discomfort, including donepezil, cholinesterase inhibitors, memantine, and statins (14, 15). However, prolonged use of these drugs can result in numerous adverse outcomes. Specifically, the increasing use of cholinesterase inhibitors results in increased adverse drug reactions, such as cardiovascular and gastrointestinal adverse effects (16); treatment with antipsychotics in older people is associated with an increased risk of cardiovascular incidents and mortality (17). Therefore, no compelling evidence supports the use of these drugs in such patients (14).

In this regard, complementary therapies could offer potential solutions to these challenges. Mind-body therapies (MBTs), rooted in ancient Eastern practices, are a non-pharmacological approach that focuses on interactions between mind, body, and spirit to improve mental and physical well-being (18, 19). Compared with other medications, MBTs are characterized by low risk and high therapeutic benefits and can be alternatives or adjuvant approaches to conventional treatments (20, 21). Common MBTs include Mindfulness training, Tai Chi, Qigong, Baduanjin, Yoga, Pilates, and Music therapy, which have been proven to exert beneficial effects on the physical and mental health of OPWD (2228). However, evidence regarding the efficacy of MBTs in managing the behavioral and psychological symptoms of dementia (BPSD) in OPWD is inconsistent, and some studies do not support the significant efficacy of MBTs in this area (2933). This study aimed to evaluate the potential multidomain benefits of MBTs for BPSD in OPWD.

2 Methods

This systematic review and meta-analysis adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 (34) and was registered in the International Prospective Register of Systematic Reviews (PROSPERO) under the registration number CRD42024559809.

2.1 Search methods

Using Medical Subject Headings in conjunction with Boolean and proximity operators, a search was conducted across six electronic databases: PubMed, Embase, Web of Science, Scopus, EBSCOhost, and APA PsycINFO, to identify relevant literature. The search covered the period from the inception of each database up to June 2024, and the strategy adhered to the Population, Intervention, Comparator, Outcome, and Study design framework. Details of the search strategy are outlined in Table 1, as per the PubMed database.

Table 1

#1Dementia* [MeSH Terms]
#2Dementia* [Title/Abstract] OR Alzheimer* [Title/Abstract] OR Amentia* [Title/Abstract]
#3#1 OR #2
#4Mind body* [Title/Abstract] OR Mind-body* [Title/Abstract] OR Mindfulness [Title/Abstract] OR Meditation [Title/Abstract] OR Shadow boxing [Title/Abstract] OR Tai Ji [Title/Abstract] OR Tai-ji [Title/Abstract] OR Tai Chi [Title/Abstract] OR Chi, Tai [Title/Abstract] OR Tai Ji Quan [Title/Abstract] OR Ji Quan, Tai [Title/Abstract] OR Quan, Tai Ji [Title/Abstract] OR Taiji [Title/Abstract] OR Taijiquan [Title/Abstract] OR T’ai Chi [Title/Abstract] OR Tai Chi Chuan [Title/Abstract] OR Qigong [Title/Abstract] OR Qi Gong [Title/Abstract] OR Ch’i Kung [Title/Abstract] OR Baduanjin [Title/Abstract] OR Yoga [Title/Abstract] OR Pilates [Title/Abstract] OR Exercise Movement Techniques [Title/Abstract] OR Movement Techniques, Exercise [Title/Abstract] OR Exercise Movement Technics [Title/Abstract] OR Pilates-Based Exercises [Title/Abstract] OR Exercises, Pilates-Based [Title/Abstract] OR Pilates Based Exercises [Title/Abstract] OR Pilates Training [Title/Abstract] OR Training, Pilates [Title/Abstract] OR Music* [Title/Abstract]
#5Older* [Title/Abstract] OR Elder* [Title/Abstract] OR Senior* [Title/Abstract] OR Aged [Title/Abstract]
#6Randomized controlled trial [Publication Type] OR Randomized [Title/Abstract] OR Placebo [Title/Abstract]
#7#3 AND #4 AND #5 AND #6

PubMed search strategy.

2.2 Inclusion and exclusion criteria

The criteria for inclusion and exclusion of studies are presented in Table 2.

Table 2

CategoryInclusion criteriaExclusion criteria
PopulationOlder people with dementia (age 60 years or older)Not older people with dementia
InterventionMind-body therapies were used as the generic term for interventions including Mindfulness training, Tai Chi, Qigong, Baduanjin, Yoga, Pilates, Music therapy, etcInterventions that were not mind-body therapies
ComparatorControl group receiving only routine treatment or appropriate rehabilitation interventionNo exclusion criteria
OutcomeAny assessment for behavioral and psychological symptoms of dementiaNo exclusion criteria
Study designAll types of randomized controlled trialsNon-randomized controlled trials, such as uncontrolled before-after trials, quasi-experiments, literature review, study protocols, conference proceedings, comments, editorial, letter to editors, etc

Inclusion and exclusion criteria.

2.3 Study selection and quality appraisal

Two independent researchers, following predefined inclusion and exclusion criteria, utilized EndNote 20.6 for study selection. After duplicates were eliminated, the remaining references were independently reviewed by both researchers based on titles, abstracts, and full texts. Quality appraisal of the included trials was conducted using the Revised Cochrane risk-of-bias tool for randomized trials, with evaluation across five bias domains: (a) randomization process, (b) deviations from intended interventions, (c) missing outcome data, (d) measurement of the outcome, and (e) selection of the reported result (35). Disagreements during study selection and quality appraisal processes were resolved through consultation with a third author.

2.4 Data extraction

Two independent researchers used a data extraction form to gather relevant information from each included trial. The extracted data comprised the following: (1) basic details such as the first author, country, and year of publication; (2) participant characteristics, including mean age (with standard deviation), sample size, and the percentage of male participants; (3) diagnostic criteria for dementia; (4) intervention and control conditions; and (5) outcome and measure.

2.5 Data synthesis

Given the differences in the measurement scales used for continuous variables (BPSD, anxiety, depression, and agitation) across the included trials, standardized mean differences (SMDs; Cohen’s d) with 95% confidence intervals (CIs) for each outcome were pooled and presented in forest plots using Stata software, version 18.0 (36). Statistical heterogeneity between trials was assessed using the chi-square test based on Q-test and I2 statistics, with a significance threshold of p-value < 0.10 (37). A sensitivity analysis was performed for each outcome using a stepwise elimination method to assess whether the pooled results were significantly affected by individual studies (36). Given the number of included trials, publication bias was examined by visual inspection of funnel plots and using Egger’s test (38, 39). The trim-and-fill method was used to assess the robustness of the findings in the presence of a publication bias (40). The certainty of evidence for each outcome was evaluated by two independent researchers using the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) guidelines (41). All statistical analyses were performed using Stata 18.0.

3 Results

3.1 Search outcomes

Searches of electronic databases and additional sources yielded 2,120 results, of which 918 were duplicates. After the titles and abstracts of the remaining 1,202 records were screened, the full text of 441 articles was assessed, resulting in 35 eligible randomized controlled trials (RCTs) (4276). After 11 additional trials with missing quantitative data were excluded, 24 were included in the meta-analyses. A PRISMA flow diagram of the literature search is presented in Figure 1.

Figure 1

3.2 Study characteristics

The 35 included trials (see Table 3) were published between 2006 and 2024 and were conducted in various countries, including China (13 trials), Italy (6 trials), the United States (4 trials), Australia (3 trials), Germany (2 trials), the Netherlands (2 trials), the United Kingdom (2 trials), Denmark, France, and Japan (one trial each). In total, 2,065 patients were assigned to the experimental group, with a mean age ranging from 76.78 to 86.56 years, while 1,978 patients were assigned to the control group, with a mean age of 76.80 to 87.20 years.

Table 3

Study IDCountryPopulationAge (Mean (SD))Total/M%Diagnostic criteriaInterventionControlOutcome (measure)
Baker et al., 2022 (42)AustraliaOPWDT: 86.00 (7.50)
C: 87.20 (6.50)
T: 45/NR
C: 50/NR
CDR/MMSEGroup musicSCDepression (MADRS)
BPSD (NPI)
Ceccato et al., 2012 (43)ItalyOPWDT: 85.50 (5.90)
C: 87.20 (7.10)
T: 27/22.2%
C: 23/17.4%
DSM-IVTraditional musicSCDepression (GDS)
Agitation (CMAI)
Chen and Pei, 2018 (44)ChinaOPWDT: 77.30 (9.40)
C: 77.30 (10.00)
T: 15/40.0%
C: 13/61.5%
Medical diagnosis/MMSE/CDRTraditional musicTAUAgitation (CMAI)
Cheng et al., 2012 (45)ChinaOPWDT: 81.00 (7.70)
C: 82.50 (7.10)
T: 12/50.0%
C: 12/25.0%
MMSE/CDRTai ChiTAUDepression (GDS)
Cheung et al., 2020 (46)ChinaOPWDT: 85.71 (6.68)
C: 85.58 (7.46)
T: 58/25.9%
C: 53/24.5%
Medical diagnosis/Global Deterioration ScaleMusic with movementTAUAgitation (CMAI)
Chu et al., 2014 (47)ChinaOPWDT+C: 82.00 (6.80)T: 49/NR
C: 51/NR
DSM-IVGroup musicTAUDepression (CSDD)
Churcher Clarke et al., 2017 (66)UKOPWDT: 81.30 (9.29)
C: 79.36 (9.91)
T: 20/40.0%
C: 11/72.7%
Medical diagnosis/MMSE/DSM-IVMindfulnessTAUAnxiety (RAID)
Depression (CSDD)
Cooke et al., 2010a (48)AustraliaOPWDT: NR
C: NR
T: 24/NR
C: 23/NR
Medical diagnosis/MMSE/DSM-IVGroup musicTAUDepression (GDS)
Cooke et al., 2010b (49)AustraliaOPWDT: NR
C: NR
T: 24/NR
C: 23/NR
Medical diagnosis/MMSE/DSM-IVGroup musicTAUAnxiety (RAID)
Agitation (CMAI)
Giulietti et al., 2023 (67)ItalyOPWDT: 82.80 (5.60)
C: 82.90 (4.20)
T: 22/36.4%
C: 22/22.7%
NINCDS-ADRDAMindfulnessNo-interventionDepression (BDI)
Guétin et al., 2009 (50)FranceOPWDT: 85.20 (6.00)
C: 86.90 (5.20)
T: 14/NR
C: 12/NR
Medical diagnosisPersonalized musicTAUAnxiety (HAMA)
Depression (GDS)
Harrison et al., 2021 (68)USAOPWDT: 79.70 (11.20)
C: 80.60 (12.60)
T: 103/28.4%
C: 55/38.0%
Medical diagnosisPersonalized musicTAUAgitation (CMAI)
Hillebrand et al., 2023 (51)GermanyOPWDT: 83.84 (7.25)
C: 84.00 (6.69)
T: 44/18.2%
C: 46/26.1%
Medical diagnosisPersonalized musicTAUBPSD (DeCS)
Huang et al., 2019 (52)ChinaOPWDT: 81.90 (6.00)
C: 81.90 (6.10)
T: 36/NR
C: 38/NR
DSM-IV/CDRTai ChiTAUDepression (GDS)
BPSD (NPI)
Lin et al., 2011 (53)ChinaOPWDT: 81.46 (7.34)
C: 82.15 (6.28)
T: 49/46.9%
C: 51/47.1%
DSM-IVGroup musicTAUAgitation (CMAI)
Liu et al., 2021 (54)ChinaOPWDT: 86.56 (4.54)
C: 86.92 (5.73)
T: 25/NR
C: 25/NR
CDRMusic with movementTAUAnxiety (HAMA)
Depression (GDS)
Lyu et al., 2018 (55)ChinaOPWDT: 68.90 (7.10)
C: 69.90 (7.90)
T: 97/41.2%
C: 95/41.1%
NINCDS-ADRDATraditional musicTAUBPSD (NPI)
McCreedy et al., 2022 (69)USAOPWDT: 79.80 (12.20)
C: 80.80 (12.10)
T: 483/32.3%
C: 493/29.2%
Medical diagnosisPersonalized musicTAUAgitation (CMAI)
Noone et al., 2023 (70)UKOPWDT: 77.80 (10.63)
C: 76.80 (4.96)
T: 10/10.0%
C: 10/40.0%
DSM-IV/MMSE/PHQMindfulnessTAUAnxiety (RAID)
Depression (CSDD)
Park et al., 2020 (56)USAOPWDT+C: 84.30 (7.70)T: 10/NR
C: 10/NR
Medical diagnosis/MMSEYogaTAUAnxiety (HADS)
Depression (HADS)
Agitation (CMAI)
Prick et al., 2024 (71)NetherlandsOPWDT: 81.70 (7.60)
C: 82.30 (9.90)
T: 49/38.8%
C: 53/45.3%
Medical diagnosisPersonalized musicTAUBPSD (NPI)
Raglio et al., 2015 (57)ItalyOPWDT: 81.70 (7.80)
C: 82.40 (6.80)
T: 32/NR
C: 35/NR
DSM-IV/CDR/MMSE/NPIPersonalized musicSCBPSD (NPI)
Raglio et al., 2010a (58)ItalyOPWDT: 85.40 (6.50)
C: 84.60 (6.80)
T: 30/3.3%
C: 30/13.3%
Medical diagnosis/MMSE/DSM-IVTraditional musicSCBPSD (NPI)
Raglio et al., 2010b (72)ItalyOPWDT: 84.00 (6.00)
C: 87.00 (6.00)
T: 10/20.0%
C: 10/30.0%
NINCDS-ADRDA
NINDS-AIREN
Traditional musicSCBPSD (NPI)
Raglio et al., 2008 (73)ItalyOPWDT: 84.40 (5.50)
C: 85.80 (5.40)
T: 30/16.6%
C: 29/13.8%
DSM-IV/MMSE/CDRTraditional musicSCBPSD (NPI)
Ridder et al., 2013 (59)DenmarkOPWDT: 82.17 (8.84)
C: 80.20 (8.67)
T: 20/NR
C: 21/NR
Medical diagnosis/MMSE/Global Deterioration ScalePersonalized musicSCAgitation (CMAI)
Sakamoto et al., 2013 (60)JapanOPWDT: 80.40 (7.41)
C: 81.54 (7.82)
T: 13/15.4%
C: 13/15.4%
DSM-IV/MMSE/CDRPersonalized musicTAUBPSD (BEHAVE-AD)
Sing et al., 2019 (61)ChinaOPWDT: 85.00 (7.10)
C: 85.70 (7.00)
T: 40/30.0%
C: 33/30.3%
Medical diagnosisGroup musicSCBPSD (NPI)
Sisti et al., 2024 (74)USAOPWDT: 79.80 (12.20)
C: 80.80 (12.10)
T: 483/32.3%
C: 493/29.2%
Medical diagnosisPersonalized musicTAUBPSD (ABMI)
Sung et al., 2006a (62)ChinaOPWDT: NR
C: NR
T: 32/NR
C: 25/NR
Medical diagnosisPersonalized musicTAUAgitation (CMAI)
Sung et al., 2006b (63)ChinaOPWDT: 76.78 (9.12)
C: 78.44 (7.85)
T: 18/61.1%
C: 18/83.3%
DSM-IV/Global Deterioration ScaleMusic with movementTAUAgitation (CMAI)
Sung et al., 2012 (64)ChinaOPWDT: 81.37 (9.14)
C: 79.50 (8.76)
T: 27/NR
C: 28/NR
Medical diagnosisGroup musicTAUAnxiety (RAID)
Agitation (CMAI)
Vink et al., 2013 (75)NetherlandsOPWDT: 82.42 (7.62)
C: 81.76 (5.72)
T: 43/32.6%
C: 34/26.5%
DSM-IVGroup musicTAUAgitation (CMAI)
Weise et al., 2020 (76)GermanyOPWDT+C: 85.05 (5.93)T: 10/NR
C: 10/NR
Medical diagnosisPersonalized musicWait-listAgitation (CMAI)
Xu et al., 2024 (65)ChinaOPWDT: NR
C: NR
T: 61/52.5%
C: 60/55.0%
Medical diagnosisGroup musicTAUDepression (CSDD)

Main characteristics of the included randomized controlled trials.

T, Test group; C, Control group; M%, Percentage of males; OPWD, Older People with Dementia; TAU, Treatment as usual; SC, Standard care; ABMI, Agitated Behavior Mapping Instrument; BPSD, Behavioral and Psychological Symptoms of Dementia; BDI, Beck Depression Inventory; BEHAVE-AD, Behavioral Pathology in Alzheimer’s Disease Rating Scale; CDR, Clinical Dementia Rating; CSDD, Cornell Scale for Depression in Dementia; CMAI, Cohen-Mansfield Agitation Inventory; DSM-IV, Diagnostic and Statistical Manual of Mental Disorders-IV; DeCS, Dementia Coding System; GDS, Geriatric Depression Scale; HAMA, Hamilton Anxiety Rating Scale; HADS, Hospital Anxiety and Depression Scale; MMSE, Mini-Mental State Examination; MADRS, Montgomery-Asberg Depression Rating Scale; NPI, Neuropsychiatric Inventory; NINCDS-ADRDA, National Institute of Neurological and Communicative Disorders and Stroke-Alzheimer’s Disease and Related Disorders Association; NINDS-AIREN, National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche et l’Enseignement en Neurosciences; PHQ, Patient Health Questionnaire; RAID, Rating Anxiety in Dementia Scale.

Among the 35 included trials, the diagnostic criteria for dementia primarily consisted of medical diagnosis, Diagnostic and Statistical Manual of Mental Disorders-IV, Mini-Mental State Examination, Clinical Dementia Rating, and the Global Deterioration Scale. The interventions included personalized music (11 trials), group music (9 trials), traditional music (6 trials), mindfulness (3 trials), music with movement (3 trials), Tai Chi (2 trials), and yoga (1 trial). The controls included treatment as usual (25 trials), standard care (8 trials), no-intervention (1 trial), and wait-list (1 trial). In addition, the deliverers of the intervention primarily included music therapists, musicians, nursing staff, psychotherapist, and trained facilitators, all of whom were qualified to be responsible for the implementation of the intervention.

3.3 Quality appraisal

The risk of bias ranged from some concern to high (see Figure 2, Table 4). The main flaws (≥10% high risk) across the included trials were the randomization process (94.3% low risk, 5.7% some concerns, and 0.0% high risk); deviations from intended interventions (45.7% low risk, 54.3% some concerns, and 0.0% high risk); missing outcome data (48.6% low risk, 48.6% some concerns, and 2.8% high risk); outcome measurement (97.2% low risk, 2.8% some concerns, and 0.0% high risk); and selection of the reported results (14.3% low risk, 77.1% some concerns, and 8.6% high risk).

Figure 2

Table 4

Study IDOutcomeDomains
D1D2D3D4D5Overall rating
Baker et al., 2022 (42)DepressionLowLowSome concernsLowSome concernsSome concerns
Baker et al., 2022 (42)BPSDLowLowSome concernsLowSome concernsSome concerns
Ceccato et al., 2012 (43)DepressionLowSome concernsLowLowLowSome concerns
Ceccato et al., 2012 (43)AgitationLowSome concernsLowLowLowSome concerns
Chen and Pei, 2018 (44)AgitationLowLowSome concernsLowLowSome concerns
Cheng et al., 2012 (45)DepressionLowSome concernsLowLowSome concernsSome concerns
Cheung et al., 2020 (46)AgitationLowLowLowLowSome concernsSome concerns
Chu et al., 2014 (47)DepressionLowLowLowLowSome concernsSome concerns
Churcher Clarke et al., 2017 (66)AnxietyLowSome concernsSome concernsLowSome concernsSome concerns
Churcher Clarke et al., 2017 (66)DepressionLowSome concernsSome concernsLowSome concernsSome concerns
Cooke et al., 2010a (48)DepressionLowLowSome concernsLowSome concernsSome concerns
Cooke et al., 2010b (49)AnxietyLowLowSome concernsLowSome concernsSome concerns
Cooke et al., 2010b (49)AgitationLowLowSome concernsLowSome concernsSome concerns
Giulietti et al., 2023 (67)DepressionLowSome concernsLowLowSome concernsSome concerns
Guétin et al., 2009 (50)AnxietyLowLowSome concernsLowSome concernsSome concerns
Guétin et al., 2009 (50)DepressionLowLowSome concernsLowSome concernsSome concerns
Harrison et al., 2021 (68)AgitationLowSome concernsSome concernsLowSome concernsSome concerns
Hillebrand et al., 2023 (51)BPSDLowSome concernsHighSome concernsLowHigh
Huang et al., 2019 (52)DepressionLowSome concernsSome concernsLowSome concernsSome concerns
Huang et al., 2019 (52)BPSDLowSome concernsSome concernsLowSome concernsSome concerns
Lin et al., 2011 (53)AgitationLowSome concernsLowLowSome concernsSome concerns
Liu et al., 2021 (54)AnxietyLowSome concernsLowLowSome concernsSome concerns
Liu et al., 2021 (54)DepressionLowSome concernsLowLowSome concernsSome concerns
Lyu et al., 2018 (55)BPSDLowSome concernsLowLowSome concernsSome concerns
McCreedy et al., 2022 (69)AgitationLowLowSome concernsLowSome concernsSome concerns
Noone et al., 2023 (70)AnxietyLowLowSome concernsLowSome concernsSome concerns
Noone et al., 2023 (70)DepressionLowLowSome concernsLowSome concernsSome concerns
Park et al., 2020 (56)AnxietyLowLowSome concernsLowSome concernsSome concerns
Park et al., 2020 (56)DepressionLowLowSome concernsLowSome concernsSome concerns
Park et al., 2020 (56)AgitationLowLowSome concernsLowSome concernsSome concerns
Prick et al., 2024 (71)BPSDLowLowLowLowHighHigh
Raglio et al., 2015 (57)BPSDLowLowSome concernsLowSome concernsSome concerns
Raglio et al., 2010a (58)BPSDLowSome concernsSome concernsLowHighHigh
Raglio et al., 2010b (72)BPSDLowSome concernsLowLowLowSome concerns
Raglio et al., 2008 (73)BPSDLowSome concernsSome concernsLowHighHigh
Ridder et al., 2013 (59)AgitationLowLowLowLowSome concernsSome concerns
Sakamoto et al., 2013 (60)BPSDLowSome concernsLowLowSome concernsSome concerns
Sing et al., 2019 (61)BPSDSome concernsLowSome concernsLowSome concernsSome concerns
Sisti et al., 2024 (74)BPSDLowLowSome concernsLowSome concernsSome concerns
Sung et al., 2006a (62)AgitationLowSome concernsLowLowLowSome concerns
Sung et al., 2006b (63)AgitationLowSome concernsLowLowSome concernsSome concerns
Sung et al., 2012 (64)AnxietyLowSome concernsLowLowSome concernsSome concerns
Sung et al., 2012 (64)AgitationLowSome concernsLowLowSome concernsSome concerns
Vink et al., 2013 (75)AgitationLowLowSome concernsLowSome concernsSome concerns
Weise et al., 2020 (76)AgitationSome concernsSome concernsLowLowSome concernsSome concerns
Xu et al., 2024 (65)DepressionLowSome concernsLowLowSome concernsSome concerns

Risk of bias summary for the included effect estimates.

BPSD, Behavioral and Psychological Symptoms of Dementia; D1, Randomization process; D2, Deviations from intended interventions; D3, Missing outcome data; D4, Measurement of the outcome; D5, Selection of the reported result.

Green for "low risk," yellow for "some concerns," and red for "high risk".

3.4 Pairwise meta-analyses

3.4.1 Effects of MBTs on BPSD

A meta-analysis of 7 RCTs (N = 564 patients) exhibited a significant improvement in BPSD (SMD = -0.33; 95% CI -0.49 to -0.16; p < 0.01) in OPWD, with no significant heterogeneity between RCTs (I2 = 43.68%; Q = 10.65; p = 0.10). A forest plot for BPSD is presented in Figure 3.

Figure 3

3.4.2 Effects of MBTs on anxiety

A meta-analysis of 6 RCTs (N = 224 patients) exhibited a significant improvement in anxiety (SMD = -0.82; 95% CI -1.53 to -0.10; p = 0.02) in OPWD, but with significant heterogeneity between RCTs (I2 = 83.69%; Q = 30.66; p < 0.01). A forest plot for anxiety is presented in Figure 4.

Figure 4

3.4.3 Effects of MBTs on depression

A meta-analysis of 10 RCTs (N = 607 patients) exhibited a significant improvement in depression (SMD = -0.57; 95% CI -1.06 to -0.08; p = 0.02) in OPWD, but with significant heterogeneity between RCTs (I2 = 87.39%; Q = 71.40; p < 0.01). A forest plot for depression is presented in Figure 5.

Figure 5

3.4.4 Effects of MBTs on agitation

A meta-analysis of 11 RCTs (N = 618 patients) exhibited no significant improvement in agitation (SMD = -0.09; 95% CI -0.25 to 0.07; p = 0.27) in OPWD, with no significant heterogeneity between RCTs (I2 = 34.66%; Q = 15.31; p = 0.12). A forest plot for agitation is presented in Figure 6.

Figure 6

3.5 Sensitivity analyses

The results of the sensitivity analyses indicated that the pooled results for agitation and BPSD remained stable after excluding individual studies, indicating that these results were robust and insensitive to study selection. However, the pooled results for anxiety and depression were sensitive to study selection and were less robust when individual studies were excluded. The results of the sensitivity analyses are presented in Table 5.

Table 5

OutcomeStudy omittedSMD95% CI
Lower boundUpper bound
BPSDBaker et al., 2022 (42)-0.37-0.56-0.19
Hillebrand et al., 2023 (51)-0.34-0.53-0.16
Huang et al., 2019 (52)-0.27-0.45-0.09
Lyu et al., 2018 (55)-0.29-0.50-0.08
Raglio et al., 2015 (57)-0.37-0.55-0.20
Raglio et al., 2010b (72)-0.34-0.51-0.17
Sakamoto et al., 2013 (60)-0.29-0.46-0.12
AnxietyCooke et al., 2010b (49)-0.95-1.81-0.09
Guétin et al., 2009 (50)-0.54-1.180.09
Liu et al., 2021 (54)-0.62-1.320.09
Park et al., 2020 (56)-1.02-1.78-0.27
Sakamoto et al., 2013 (60)-0.84-1.700.01
Sung et al., 2012 (64)-0.93-1.82-0.03
DepressionBaker et al., 2022 (42)-0.61-1.16-0.07
Ceccato et al., 2012 (43)-0.65-1.16-0.14
Cheng et al., 2012 (45)-0.57-1.10-0.05
Chu et al., 2014 (47)-0.56-1.130.01
Cooke et al., 2010a (48)-0.64-1.16-0.13
Guétin et al., 2009 (50)-0.58-1.11-0.05
Huang et al., 2019 (52)-0.42-0.880.04
Liu et al., 2021 (54)-0.60-1.14-0.07
Park et al., 2020 (56)-0.62-1.14-0.11
Xu et al., 2024 (65)-0.43-0.850.01
AgitationCeccato et al., 2012 (43)-0.12-0.290.05
Chen and Pei, 2018 (44)-0.10-0.270.06
Cheung et al., 2020 (46)-0.11-0.290.06
Cooke et al., 2010b (49)-0.09-0.260.07
Lin et al., 2011 (53)-0.06-0.230.11
Park et al., 2020 (56)-0.11-0.270.05
Ridder et al., 2013 (59)-0.08-0.240.09
Sing et al., 2019 (61)-0.08-0.250.09
Sung et al., 2006a (62)-0.04-0.210.12
Sung et al., 2006b (63)-0.05-0.220.11
Sung et al., 2012 (64)-0.14-0.310.03

Sensitivity analyses for outcomes by omitting individual studies.

SMD, Standardized mean difference; CI, Confidence interval; BPSD, Behavioral and Psychological Symptoms of Dementia.

3.6 Publication bias and certainty of evidence

Given the number of included trials with pooled results for depression and agitation, publication bias was assessed using funnel plots and the Egger’s test. Funnel plots for depression and agitation are presented symmetrically in Figure 7. The p-values of Egger’s test for depression and agitation were 0.42 and 0.55, respectively, indicating that publication bias did not affect this type of study. According to the GRADE ratings, the certainty of evidence across the outcomes ranged from low to very low, owing to inconsistency, indirectness, imprecision, and publication bias (see Table 6).

Figure 7

Table 6

OutcomeRisk of biasInconsistencyIndirectnessImprecisionPublication biasCertainty of the
evidence
BPSDNo downgrade, as trials at high risk of bias constituted less than 30%.Downgrade by one level due to unexplained inconsistency (I2 = 43.68%).Downgrade by one level due to the inclusion of certain participants (OPWD).No concerns (SMD = -0.33; 95% CI -0.49 to -0.16)./⊕⊕⊝⊝
Low
AnxietyNo downgrade, as trials at high risk of bias constituted less than 30%.Downgrade by two levels due to unexplained inconsistency (I2 = 83.69%).Downgrade by one level due to the inclusion of certain participants (OPWD).No concerns (SMD = -0.82; 95% CI -1.53 to -0.10)./⊕⊝⊝⊝
Very low
DepressionNo downgrade, as trials at high risk of bias constituted less than 30%.Downgrade by two levels due to unexplained inconsistency (I2 = 87.39%).Downgrade by one level due to the inclusion of certain participants (OPWD).No concerns (SMD = -0.57; 95% CI -1.06 to -0.08).No publication bias is suspected.⊕⊝⊝⊝
Very low
AgitationNo downgrade, as trials at high risk of bias constituted less than 30%.Downgrade by one level due to unexplained inconsistency (I2 = 34.66%).Downgrade by one level due to the inclusion of certain participants (OPWD).Some concerns (SMD = -0.09; 95% CI -0.25 to 0.07). Downgrade by one level.No publication bias is suspected.⊕⊝⊝⊝
Very low

Certainty of evidence rating (GRADE).

SMD, Standardized mean difference; CI, Confidence interval; I2, Heterogeneity index in percentage (range: 0-100%); BPSD, Behavioral and Psychological Symptoms of Dementia; OPWD, Older People with Dementia.

4 Discussion

Previous studies have predominantly investigated the efficacy of single interventions for OPWD and have provided inconsistent evidence regarding various outcomes (2333). This study aimed to evaluate the potential multidomain benefits of MBTs for BPSD in OPWD. The pooled results of the meta-analyses indicated that MBTs effectively improved BPSD (SMD = -0.33; 95% CI -0.49 to -0.16; p < 0.01), anxiety (SMD = -0.82; 95% CI -1.53 to -0.10; p = 0.02), and depression (SMD = -0.57; 95% CI -1.06 to -0.08; p = 0.02), with no significant improvements observed in agitation (SMD = -0.09; 95% CI -0.25 to 0.07; p = 0.27) among patients with dementia.

Music-based interventions are likely the most common MBT for alleviating BPSD in OPWD, as evidenced in 26 of the 35 trials. Previous studies have confirmed the effectiveness of music-based interventions, particularly in improving anxiety and depression (7781). Music-based interventions are among the most effective approaches for managing BPSD in OPWD. However, a recent systematic review revealed that music-based interventions may not have achieved the anticipated efficacy, suggesting that the generalizability and applicability of this evidence require further examination (82). Overall, MBTs have significant therapeutic benefits in alleviating BPSD in OPWD, and the underlying mechanisms may be explained from several perspectives. Dementia is associated with the hypothalamus-pituitary-adrenal (HPA) axis and the autonomic nervous system (ANS), which are the main components of emotional regulation (83, 84). By reducing the HPA axis activation and reactivity, MBTs may alleviate the effects of stress and foster multiple positive downstream effects by shifting the ANS balance from primarily sympathetic to parasympathetic, leading to positive changes in cardiac vagal function, mood, energy state, and related neuroendocrine, metabolic, and inflammatory responses (8589), which may play a potential role in mediating BPSD in OPWD. In addition, an increase in neurotransmitters such as serotonin and dopamine (responsible for regulating emotions and behavior) can be induced through exercise interventions included in MBTs (e.g., Tai Chi, Qigong, and Yoga), which help improve BPSD in OPWD (90).

BPSD represents a heterogeneous group of non-cognitive symptoms and behaviors that occur in patients with dementia, including anxiety, depression, agitation, irritability, apathy, and delusions (9193). Therefore, in the quantitative analysis, BPSD was subdivided based on existing data to further clarify the efficacy of MBTs for these specific symptoms. Although the pooled results of the meta-analyses indicated that MBTs effectively improved BPSD in OPWD, this impact did not include all symptoms. For instance, according to the pooled results for agitation in OPWD, MBTs did not provide significant therapeutic benefits as previously assumed, which is consistent with previous evidence (30, 32). This may be because, for OPWD, especially those with advanced dementia, the inability to perform activities of daily living, often accompanied by clinical complications such as dysphagia and infections (14), presents a significant challenge in addressing behavioral disorders (including agitation and aggressive tendencies) with short-term MBTs. Finally, in terms of improving anxiety and depression in OPWD, evidence confirming the therapeutic benefits of MBTs is urgently required because of the significant heterogeneity or sensitivity to study selection in the pooled results. This may stem from the fact that the specific interventions, implementation steps, and duration of the interventions varied between studies, resulting in large differences in effect sizes. Additionally, the CIs for certain pooled results were near the threshold of statistical significance after excluding individual studies. This indicates that the sample size and experimental design need to be further increased and refined to more precisely evaluate the potential benefits of MBTs on these outcomes.

Although MBTs are promising complementary therapies for enhancing physical and mental health in OPWD, their differential efficacy should be further explored and validated. Most existing trials focus on the efficacy of a single intervention for BPSD in OPWD while ignoring the differential efficacy between various interventions. This may lead to an overestimation of the actual efficacy of MBTs in clinical practice. In the context of limited medical resources and the increasing prevalence of dementia, MBTs that can be effectively applied to clinical practice should be identified. Doctors and nurses are inclined to use non-pharmacological treatments more than pharmacological treatments in clinical practice (94). Therefore, comparisons between non-pharmacological treatments should receive more attention. A network meta-analysis suggests that individualized nursing, behavior therapy, and reminiscence therapy have significant potential in improving BPSD in OPWD, particularly in reducing anxiety and depression (95). Thus, the differential efficacy of non-pharmacological treatments in improving various aspects of BPSD should be further examined to maximize the clinical benefits of non-pharmacological treatments in the context of limited medical resources. Notably, the efficacy of MBTs in improving BPSD in OPWD may vary depending on the intervention period, frequency, and duration, suggesting that the dose-response relationship of MBTs in this regard is also an important area for investigation. Although this study did not reveal the optimal dosage of MBTs for improving BPSD in OPWD, existing research indicates that the intervention period, frequency, and duration are critical factors influencing efficacy (31, 33, 96). Short-term, high-frequency interventions may lead to faster clinical improvements to some extent, while long-term, low-frequency interventions may help maintain long-term efficacy. Therefore, more high-quality RCTs must be conducted to explore the dose-response relationship of MBTs in improving BPSD in OPWD, and intervention programs should be flexibly adjusted in clinical practice based on patients’ individual differences to achieve the best therapeutic outcomes.

5 Limitations

The findings of this systematic review and meta-analysis should be interpreted in the context of these limitations. First, owing to the limited information available on the study population from existing trials, this study mainly examined the overall therapeutic benefit of MBTs for OPWD and did not make specific distinctions based on the type and course of dementia. Second, although there was significant heterogeneity in the pooled results for some outcomes, sources of heterogeneity were not identified because of study data limitations. To address this problem, more comprehensive data should be collected in future studies. Finally, for some outcomes such as anxiety and depression, the pooled results were sensitive to study selection and were less robust; thus, the findings should be interpreted cautiously.

6 Conclusions

Effective nursing for patients with dementia is vital, as they are undergoing a major transition in their physical and mental health. Although MBTs effectively improved BPSD in OPWD to some extent, the dose-response relationship of MBTs in improving various aspects of BPSD remains unclear, and these relationships may be influenced by the intervention period, frequency, and duration. In clinical practice, healthcare and social care therapists should develop personalized intervention programs based on patient individual differences and the actual dose-response relationship, which will help maximize the clinical benefits of non-pharmacological treatments in the context of limited medical resources.

Statements

Data availability statement

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

Author contributions

ZYM: Conceptualization, Data curation, Methodology, Resources, Software, Writing – original draft, Writing – review & editing. CYC: Conceptualization, Formal analysis, Methodology, Software, Writing – original draft, Writing – review & editing. TFW: Data curation, Resources, Visualization, Writing – original draft. YZZ: Formal analysis, Validation, Writing – original draft, Software. WZ: Conceptualization, Data curation, Software, Writing – review & editing. CFL: Methodology, Software, Visualization, Writing – review & editing. SLL: Data curation, Writing – review & editing, Validation, Visualization. YS: Validation, Visualization, Writing – review & editing. SL: Funding acquisition, Methodology, Project administration, Supervision, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This research was funded by the National Social Science Fund of China (project 24BTY098).

Acknowledgments

Research team would like to thank Southwest University for the support of this research, and also thank Shi Luo for the help in developing the research program.

Conflict of interest

The 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.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

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.

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Summary

Keywords

mind-body therapies, older people, dementia, mental health, gerontology

Citation

Mei Z, Cai C, Wang T, Zhang Y, Zhao W, Lam C, Luo S, Shi Y and Luo S (2025) Are mind-body therapies beneficial for older people with dementia? A Systematic Review and meta-analysis of randomized controlled trials. Front. Psychiatry 16:1569709. doi: 10.3389/fpsyt.2025.1569709

Received

01 February 2025

Accepted

12 March 2025

Published

14 April 2025

Volume

16 - 2025

Edited by

Yibo Wu, Peking University, China

Reviewed by

Andrew Clifton, University of Suffolk, United Kingdom

Nur Melizza, Universitas Muhammadiyah Malang, Indonesia

Updates

Copyright

*Correspondence: Shi Luo,

Disclaimer

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.

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