Abstract
Background:
Strengthening the pelvic floor muscles through non-invasive Kegel exercises before the onset of clinical symptoms is the most effective method for reducing postpartum complications.
Aim:
This study seeks to investigate the impact of the Kegel exercise on maternal postpartum pain, pelvic floor dysfunction, and sexual function among women in the obstetrics and gynecology department of the National Guard Hospital, King Abdul-Aziz Medical City, Jeddah, Saudi Arabia.
Methods:
a quasi-experimental design with six weeks apart pre- and post-tests was used, having 31 participants per group recruited with a convenience sample method. An interviewer-administered questionnaire containing a 20-item Pelvic Floor Disability Index (PFDI-20), a 19-item Female Sexual Function Index (FSFI), and the Visual Analog Scale with the Faces Pain Rating Scale was used to measure pelvic floor dysfunction, sexual function, and postpartum pain, respectively. These tools were valid and reliable.
Results:
Results revealed a significant increase in the Female Sexual Function Index in the experimental group after the intervention and a substantial decrease in the Visual Analog Scale with the Face Pain Rating Scale in both groups after the intervention. There were no statistically significant differences between the experimental and control groups in the total score of pelvic floor dysfunction. However, the Colorectal-Anal Distress Inventory subscale showed a substantial increase in the control group post-test. In conclusion, the current study has shown that Kegel exercises can increase sexual drive and reduce pain in women with postpartum complications.
Introduction
Childbirth can lead to complications such as pelvic floor weakness, pain, and ligament laxity, which may negatively affect women's sexual function and overall quality of life (). Postpartum pain is a common complication and an important factor influencing various aspects of women's recovery, including physical function, psychological well-being, sleep, breastfeeding effectiveness, and bonding between mother and newborn (). In a systematic review, Sultan and colleagues () reported that up to 18% of women experienced postpartum pain 12 months after a Cesarean section, while approximately 10% experienced persistent pain up to 18 months following any delivery method.
Another common postpartum complication is pelvic floor dysfunction (PFD), resulting from the impact of labor on pelvic muscle structures (, ). The pelvic floor muscles and connective tissues play a vital role in maintaining the stability of the pelvis, abdomen, and lower urinary tract (). Consequently, these structures are susceptible to weakening or injury during labor and delivery, impairing their optimal function (–). In a meta-analysis, Barca and colleagues () reported that the most prevalent pelvic floor disorders among postpartum women were urinary incontinence (27.9%), pelvic organ prolapse (14.2%), and anal incontinence (0.4%). These complications could have serious impacts on the patient's body, mind, and social life and negatively impact their quality of life (, –).
Furthermore, postpartum sexual dysfunction is a notable complication often resulting from factors such as body image changes, fatigue, lack of sleep, and urinary stress or urge symptoms (, ). Sexual function typically declines after delivery and rarely returns to pre-pregnancy levels during the postpartum period, as many women report difficulties affecting sexual desire and relationships (, ). The prevalence of postpartum sexual dysfunction has been reported to range from 41% to 83% (–). In a study by Dawson and colleagues, nearly half of the participants experienced sexual dysfunction three months postpartum ().
Medications and surgical interventions are available to manage postpartum discomfort, pelvic floor dysfunction, and erectile dysfunction (). However, evidence indicates that pregnant and postpartum women should be encouraged to engage in exercise for both physical and mental well-being, with pelvic floor muscle training integrated into routine workouts to mitigate postpartum complications ().
Several studies have shown that training the pelvic floor muscles can reduce the risk of postpartum issues and associated symptoms, provided that the exercises are initiated before clinical symptoms appear (). This non-invasive intervention, known as Kegel exercise (), involves repetitive contractions of the pelvic muscles that control urination, aiming to strengthen the pelvic floor, prevent or manage incontinence, reduce postpartum pain, and improve sexual responsiveness (). Kegel exercises are also referred to as pelvic muscle strengthening exercises or pelvic floor exercises (PFE) (, ).
The researcher aims for this study to contribute to midwifery knowledge by highlighting how Kegel exercises can enhance the health and quality of life of postpartum women.
Significance of the study
In Saudi Arabia, data on the prevalence of pelvic floor dysfunction remain limited, hindering the development of effective treatment strategies. Previous studies have assessed the benefits of Kegel exercises during pregnancy and for managing postpartum complications such as pelvic dysfunction and sexual impairment (–). However, a 2019 cross-sectional study in Madinah revealed that 57% of women had never practiced Kegel exercises, mainly due to inadequate educational programs (). To date, no studies have evaluated the effects of these exercises on maternal postpartum pain, pelvic floor dysfunction, or sexual function among Saudi women. Consequently, the present study aims to examine these outcomes among women in Jeddah, providing essential evidence to support midwifery practice and enhance postpartum recovery and quality of life.
Aim of the study
This study aims to identify the impact of the Kegel exercise on maternal postpartum pain, pelvic floor dysfunction, and sexual function among women in Jeddah, Saudi Arabia.
Hypothesis
Null hypothesis
Training on Kegel exercises has no significant effect on pain, pelvic floor dysfunction, or sexual function among postpartum women.
Conceptual framework
The General System Model, proposed by Ludwig von Bertalanffy (1968), provides the theoretical foundation for this study (Figure 1), emphasizing that systems consist of interrelated and dynamic components that interact with their environment (, ). Each system includes three key elements: input, throughput, and output, where inputs are transformed into outcomes through specific processes. Sustaining a system requires clear goals, feedback mechanisms, and adaptability to environmental changes (). Within this study, the model is applied such that inputs represent the preparatory phase (interviews and assessments), throughput reflects the performance and adherence to Kegel exercises, and outputs denote the resulting maternal outcomes.
Figure 1
Methodology
Research design
This study used a quantitative quasi-experimental pre- and post-test design, which effectively tests cause-and-effect relationships and provides strong evidence of intervention efficacy (
Study area/setting
The postnatal women who participated in this study were recruited from the obstetrics and gynecology department of the National Guard Hospital located in King Abdul-Aziz Medical City in Jeddah, Saudi Arabia.
Study population
The postnatal women in the obstetrics and gynaecology department in the King Abdul-Aziz Medical City, Jeddah, Saudi Arabia.
Inclusion and exclusion criteria
Inclusion criteria include women who were ≤6 weeks postpartum, aged 18–45 years, multiparous, had a vaginal delivery, and were able to communicate in Arabic or English. Exclusion criteria included women with urinary or gastrointestinal infections, inflammatory conditions, significant comorbidities, or cognitive and behavioral impairments, to prevent potential confounding effects on the study outcomes.
Sampling and sampling technique
The sampling technique adopted for this study is the convenience sampling method to recruit study subjects who have given their consent and met the study's inclusion criteria after institutional review board approval is obtained from the King Abdullah International Medical Research Center. The sample was randomly allocated into control and experimental groups using SPSS software as a simple randomization allocation.
Sample size
Using G*Power 3.1.9.7, the necessary sample size was determined. An earlier Cochrane evaluation estimated the effect size of Kegel and other pelvic floor muscle training for preventing and treating mild problems in pregnant and postpartum women (
Research tools
Pelvic floor dysfunction (PFD) assessment/pelvic floor disability index (PFDI-20)
This tool was used by Artymuk and Khapacheva (
Female sexual function index (FSFI)
The FSFI is a 19-item self-report tool that evaluates female sexual function, as used in prior investigations (
Pain and functional disability assessment
The Visual Analog Scale (VAS) instrument was developed by Hayes & Patterson in 1921, and it is commonly utilized to evaluate states such as anxiety, despair, weariness, and pain (
Figure 2

Visual analog scale (VAS) (
Data collection procedure
Data were collected using an interviewer-administered questionnaire describing the sociodemographic, obstetric characteristics, Pelvic Floor Disability Index, Female Sexual Function Index, and the Pain and Functional Disability Assessment of respondents.
The data collection was conducted through three phases:
First: preparation phase: Here, institutional review board approval was obtained from the King Abdullah International Medical Research Center, and the participating women's written consent was obtained. Orientation about the study to participants was provided, ensuring it was standardized for all participants; their contact number was collected, and social network groups were created.
Second: Intervention Implementation Procedures: Participants completed questionnaires for a pre-test. The experimental group received an orientation on Kegel exercise training, supported by a video demonstrating the function of the pelvic floor muscles and Kegel procedures, as adopted from Gustirini et al. (
Third: Evaluation Phase: The Pelvic Floor Disability Index, Female Sexual Function Index, and pain assessment questionnaires were completed as a post-test for all participants (after six weeks) through an electronic link to the questionnaire via WhatsApp for the two groups.
Data analysis
Using the International Business Machines-Statistical Package for Social Sciences (IBM-SPSS) version 29 for Windows, the obtained data were coded, entered, and analyzed. The demographic data's descriptive statistics were analyzed using frequency, percentages, and mean analyses. The Univariate Analysis of Variance (ANCOVA) and Student's t-test were used to determine any significant differences between the study groups on the study variables. Repeated measures multivariate analysis of variance (MANOVA) was used to analyze within and between-group differences of all variables in both groups. P-value < 0.05 was considered significant. Effect size (Cohen's d) was calculated as the between-group difference divided by the pooled standard deviation at baseline. Effect sizes of 0.20, 0.50, and 0.80 were considered small, moderate, and large, respectively (Suggested by Cohen). A Pearson's Correlation was run to determine the relationship between pre- and post-tests for the four domains and participants’ personal data and pregnancy history.
Validity and reliability
To ensure the reliability and validity, relevance, language clarity, and applicability of the study tool were tested. The coefficient alpha (or Cronbach's alpha) is the most commonly used statistic for measuring internal consistency (
The study also employed construct and face validity. The research instrument's face validity was ensured through a questionnaire review with two senior lecturers. After the completion of the questionnaire, construction of its items, and presenting it to the research supervisor's Excellency, the questionnaire was translated into the Arabic language and presented in its modified form to a group of arbitrators, and after retrieving the arbitrated version, their notes were discussed with the supervisor's Excellency of the thesis. Considering some arbitrators’ suggestions, the researcher reworded the questionnaire, where some of the coefficient values were high, indicating the availability of a high degree of internal consistency validity for the questionnaire's items.
Ethical consideration
This research was authorized by the Institutional Review Board (IRB) at King Abdul-Aziz Medical City-Western Region and the College of Nursing Research Unit of the King Abdullah International Medical Research Center (KAIMRC) [IRB/1251/22, study number SP22J/060/05], Jeddah. Additionally, hospital administrative personnel were contacted before data collection, written informed consent was obtained from participants who met the criteria for inclusion to participate in the current study, and participation was voluntary. Furthermore, privacy, confidentiality, and anonymity were maintained.
Trial registration
This study adopted a quasi-experimental design to assess the effect of Kegel exercises on postpartum outcomes. As the intervention was behavioral and non-pharmacological, it did not meet the criteria for a clinical trial requiring prospective registration according to WHO guidelines. The study protocol was approved by the Institutional Ethical Committee (Approval No.: [IRB/1251/22, study number SP22J/060/05), and written informed consent was obtained from all participants before data collection.
Results
In this study, the mean age of the control group is 30.13 ± 5.46, and the experimental group is 30.74 ± 5.37. Almost all (control group = 100%, experimental group = 96.7%) of the studied women were married. Also, it was noted that more than two-thirds of the sample (control group = 67.7%, experimental group = 73.3%) held a bachelor's degree, and one quarter (control group = 25.8%, experimental group = 23.3%) of the women finished high school. Also, the table presents that less than three quarters (control group = 67.7%, experimental group = 73.3%) of the women were non-working, whilst more than one quarter (control group = 32.3%, experimental group = 26.7%) of them were working. More than half (control group = 58.1%, experimental group = 50%) of the women reported an average monthly income, and almost all the sample was from an urban place of residence (control group = 90.3%, experimental group = 93.3%). Also, the Unpaired t-test showed a non-significant difference (p > 0.05) between the two groups in age. Furthermore, the table demonstrated that there were no statistically significant differences between the two study groups regarding their sociodemographic data (Table 1).
Table 1
| Demographic and personal characteristics | Groups | Test of Significance (P-value) | ||||
|---|---|---|---|---|---|---|
| Control group | Experimental group | |||||
| n.31 | % | n.30 | % | |||
| Age | t = −.446 (0.657) | |||||
| Mean ± SD | 30.13 ± 5.46 | 30.74 ± 5.37 | ||||
| Min-max | 20–40 | 21–40 | ||||
| Marital status | Married | 31 | 100.0% | 29 | 96.7% | X2 = 1.016 (.313) |
| Divorced | 0 | 0.0% | 1 | 3.3% | ||
| Education | Secondary | 1 | 3.2% | 0 | 0.0% | X2 = 1.023 (.796) |
| High school | 8 | 25.8% | 7 | 23.3% | ||
| Bachelor's degree | 21 | 67.7% | 22 | 73.3% | ||
| High degrees | 1 | 3.2% | 1 | 3.3% | ||
| Working condition | Working | 10 | 32.3% | 8 | 26.7% | X2 = .313 (.576) |
| Non-working | 21 | 67.7% | 22 | 73.3% | ||
| Monthly income | Enough | 11 | 35.5% | 15 | 50.0% | X2 = 1.221 (.543) |
| Average | 18 | 58.1% | 15 | 50.0% | ||
| Insufficient | 2 | 6.5% | 0 | 0.0% | ||
| Place of residence | Rural | 3 | 9.7% | 2 | 6.7% | |
| Urban | 28 | 90.3% | 28 | 93.3% | ||
Distribution of the study groups (control and experimental group) according to their demographic and personal characteristics (n.61).
Descriptive statistics, t, t-test; ×2, chi-square, p ≤ 0.05.
As shown in Table 2 below, more than half of the control group (58.1%) and less than three-quarters (70.0%) of the experimental group had no miscarriages. Whilst more than one-third (32.3%) of the control group and more than one-quarter (26.7%) of the experimental group had one to three miscarriages. Regarding the type of delivery of the women's last birth, more than three-quarters of the control and the experimental groups gave birth to their last child vaginally (77.4% and 83.3%, respectively). Less than one-quarter of the control and the experimental groups gave birth to their last child by an interventional delivery (22.6% and 16.7%, respectively). Also, the Unpaired t-test showed no significant difference (p > 0.05) in the number of children between the two groups. There were no statistically significant differences between the two study groups regarding their previous pregnancy history (Table 2).
Table 2
| Previous pregnancy history | Groups | Significant differences tests | ||||
|---|---|---|---|---|---|---|
| Control group | Experimental group | |||||
| n.31 | % | n.30 | % | Fisher-exact test (sig.) | ||
| Miscarriage | No miscarriage | 18 | 58.1 | 21 | 70.0 | FET = 1.387 (0.749) |
| 1–3 miscarriage | 10 | 32.3 | 9 | 26.7 | ||
| >3 miscarriage | 3 | 9.7 | 1 | 3.3 | ||
| Type of delivery | Vaginal delivery | 24 | 77.4 | 26 | 83.3 | FET = 1.437 (0.503) |
| Interventional/instrumental delivery | 7 | 22.6 | 5 | 16.7 | ||
| Number of children | ||||||
| Mean ± SD | 3.35 ± 1.78 | 2.90 ± 1.56 | t-test (p-value) −1.059 (.294) | |||
| Min-max | 1.00–8.00 | 1.00–7.00 | ||||
Distribution of the study groups (control and experimental group) according to their previous pregnancy history (n.61).
Descriptive statistics, t, t-test, FET, fisher-exact test, p ≤ 0.05.
Table 3 presents the Item-level descriptive analysis of the PFDI-20, showing mild to moderate pelvic floor symptoms at baseline in both groups. After Kegel exercise training, the experimental group demonstrated numerical improvements in several prolapse-related, colorectal-anal, and urinary symptoms. However, similar variations were also observed in the control group, suggesting natural postpartum recovery. Given the small magnitude of change and overlapping variability, item-level findings were interpreted cautiously, and conclusions regarding intervention effectiveness were based primarily on domain-level and total PFDI-20 scores, which offer greater clinical and statistical robustness.
Table 3
| Pelvic floor disability index (PFDI-20) | Time point | Control group (n.31) Mean ± SD | Experimental group (n.30) Mean ± SD |
|---|---|---|---|
| Pelvic organ prolapse distress inventory-6 (POPDI-6) | |||
| 1. Pressure in the lower abdomen | Baseline | .9 ± 1.4 | 1 ± 1.3 |
| After training | .7 ± 1.2 | 1.2 ± 1.2 | |
| 2. Heaviness/dullness in the pelvic area | Baseline | 1.2 ± 1.4 | 1.3 ± 1.3 |
| After training | 1.0 ± 1.3 | 1.0 ± 1.1 | |
| 3. Bulge/prolapse sensation | Baseline | .8 ± 1.2 | .6 ± 1.1 |
| After training | .9 ± 1.5 | .8 ± .9 | |
| 4. Push the vagina/rectum for bowel movement | Baseline | 1.3 ± 1.3 | 1.0 ± 1.3 |
| After training | .9 ± 1.3 | 1.1 ± 1.2 | |
| 5. Incomplete bladder emptying | Baseline | 1.3 ± 1.4 | 1.2 ± 1.3 |
| After training | .6 ± 1.0 | 1.0 ± 1.1 | |
| 6. Push up bulge to urinate | Baseline | .5 ± 1.0 | .5 ± .8 |
| After training | .3 ± .8 | .5 ± .8 | |
| Colorectal-Anal Distress Inventory subscale (CRAD) | |||
| 7. Straining during bowel movement | Baseline | 1.5 ± 1.4 | 1.1 ± 1.3 |
| After training | .8 ± 1.3 | 1.3 ± 1.3 | |
| 8. Incomplete bowel emptying | Baseline | 1.3 ± 1.3 | 1.0 ± 1.1 |
| After training | 1.0 ± 1.3 | 1.3 ± 1.4 | |
| 9. Stool leakage (solid) | Baseline | .8 ± 1.2 | .6 ± 1.0 |
| After training | .5 ± 1.0 | 1.0 ± 1.2 | |
| 10. Stool leakage (loose) | Baseline | 1.0 ± 1.2 | .6 ± 1.0 |
| After training | .5 ± 1.0 | .9 ± 1.1 | |
| 11. Gas leakage | Baseline | 1.3 ± 1.2 | .9 ± 1.0 |
| After training | .8 ± 1.3 | 1.3 ± 1.3 | |
| 12. Pain with bowel movement | Baseline | 1.1 ± 1.2 | .7 ± 1.0 |
| After training | 1.0 ± 1.4 | 1.4 ± 1.3 | |
| 13. Fecal urgency | Baseline | 1.1 ± 1.3 | .8 ± 1.0 |
| After training | .8 ± 1.3 | 1.2 ± 1.2 | |
| 14. Rectal prolapse sensation | Baseline | .8 ± 1.2 | .5 ± .8 |
| After training | .4 ± .9 | .9 ± 1.2 | |
| Urinary distress inventory-6 (UDI-6) | |||
| 15. Frequent urination | Baseline | 1.1 ± 1.0 | 1.4 ± 1.3 |
| After training | .8 ± 1.3 | 1.4 ± .9 | |
| 16. Urgency-related leakage | Baseline | 1.1 ± 1.2 | 1.2 ± 1.2 |
| After training | .7 ± 1.2 | 1.1 ± .9 | |
| 17. Stress urinary leakage | Baseline | 1.0 ± 1.1 | 1.0 ± 1.1 |
| After training | .8 ± 1.1 | 1.2 ± 1.0 | |
| 18. Small urine leakage | Baseline | .8 ± 1.1 | 1.0 ± 1.1 |
| After training | .6 ± 1.0 | 1.0 ± 1.0 | |
| 19. Difficulty emptying bladder | Baseline | .8 ± 1.1 | .8 ± 1.1 |
| After training | .5 ± 1.1 | 1.0 ± 1.0 | |
| 20. Lower abdominal/genital pain | Baseline | .9 ± 1.1 | .9 ± 1.3 |
| After training | 1.0 ± 1.3 | 1.4 ± 1.1 | |
Descriptive item-level distribution of pelvic floor disability Index (PFDI-20) symptoms At baseline and after Kegel exercise training Among the control and experimental groups.
Table 4 summarises the mean values of all PFDI-20 subscales at baseline and after intervention in both groups. The t-test revealed statistically significant differences in the Colorectal-Anal Distress Inventory (CRAD) between the control and experimental groups at P = 0.014. It was also identified that there was a significant increase in CRAD scores in the control group after the test, with a mean score of 28.73 ± 26.47. ANCOVA showed no statistical differences between the experimental and control groups in the total score of pelvic floor dysfunction (Table 3).
Table 4
| Domains | Maximum allowed score | Group | Significance test independent samples t-test | Univariate analysis of variance (ANCOVA) | |||
|---|---|---|---|---|---|---|---|
| Control group n.31 | Experimental group n.30 | ||||||
| M ± SD | M ± SD | t | p-value | ||||
| Pelvic organ prolapse distress inventory (POPDI) | Baseline | 100 | 22.58 ± 22.30 | 24.86 ± 24.92 | −1.096 | .277 | F = 3.368 p-value = .072 |
| After Kegel exercise training | 23.39 ± 20.46 | 18.19 ± 26.11 | |||||
| Colorectal-anal distress inventory (CRAD) | Baseline | 100 | 18.45 ± 19.55 | 28.12 ± 25.27 | −2.531 | .014* | |
| After Kegel exercise training | 28.73 ± 26.47 | 17.81 ± 25.59 | |||||
| Urinary distress inventory 6 (UDI-6) | Baseline | 100 | 26.34 ± 26.14 | 23.19 ± 22.58 | −21.148 | .256 | |
| After Kegel exercise training | 29.70 ± 20.38 | 18.33 ± 25.79 | |||||
| Pelvic floor disability index (PFDI) | Baseline | 300 | 67.37 ± 60.14 | 76.18 ± 66.70 | 1.845 | .070 | |
| After Kegel exercise training | 81.82 ± 59.81 | 54.34 ± 74.23 | |||||
Univariate analysis of variance (ANCOVA) and independent samples t-test for PFDI-20 subscales in both groups (control and experimental).
Descriptive statistics, t, t-test; F, ANCOVA; NB, The higher mean means an increase in pelvic floor disability.
Significant at p ≤ 0.05.
Table 5 shows the Item-level FSFI analysis, which showed mild to moderate sexual desire and arousal at baseline with comparable scores between groups. After training, the experimental group exhibited modest and variable numerical changes, while the control group showed increases across several items, likely reflecting natural postpartum recovery. Given the small changes and overlapping variability, item-level findings were interpreted descriptively, and conclusions regarding intervention effects were based on domain-level and total FSFI scores.
Table 5
| Female sexual function index (FSFI) (over the past 4 weeks) | Time point | Control group (n.31) Mean ± SD | Experimental group (n.30) Mean ± SD |
|---|---|---|---|
| Desire | |||
| Frequency of sexual desire or interest | Baseline | 2.5 ± 1.2 | 3.0 ± 1.0 |
| After training | 3.2 ± 1.0 | 2.7 ± 1.1 | |
| Level (degree) of sexual desire or interest | Baseline | 3.0 ± .8 | 2.8 ± .8 |
| After training | 3.4 ± 1.0 | 2.5 ± .8 | |
| Arousal | |||
| Frequency of sexual arousal (“turned on”) | Baseline | 2.8 ± 1.3 | 2.8 ± 1.2 |
| After training | 3.3 ± 1.2 | 2.3 ± .9 | |
| Level of sexual arousal (“turn on”) | Baseline | 2.9 ± .8 | 2.7 ± .9 |
| After training | 3.4 ± .8 | 2.8 ± .6 | |
| Confidence in becoming sexually aroused | Baseline | 3.1 ± 1.1 | 3.2 ± .9 |
| After training | 3.4 ± 1.3 | 2.8 ± .9 | |
| Satisfaction with sexual arousal | Baseline | 3.3 ± 1.3 | 3.3 ± 1.2 |
| After training | 3.4 ± 1.2 | 2.7 ± .9 | |
Descriptive item-level distribution of female sexual function Index (FSFI) desire and arousal items At baseline and after Kegel exercise training Among the control and experimental groups.
Furthermore, Table 6 presents the mean values of all Female Sexual Function Index (FSFI) domains at baseline and after intervention in both groups. T-tests for both groups specified that there were statistically significant differences in desire and arousal domains of the Female Sexual Function Index (FSFI) (.009,.005, and.002), respectively. They illustrated that higher scores in both FSFI domains, Desire and Arousal, were indicated for the experimental group after the Kegel exercise training intervention, with a mean of (3.92 ± 1.11, 4.08 ± 1.22), respectively. Moreover, ANCOVA showed that the differences between the control and experimental groups are statistically significant in FSFI (F = 12.333, p-value = .001*) (Table 6).
Table 6
| The female sexual function index | Maximum allowed score | Group | Significance test independent samples t-test | Univariate analysis of variance (ANCOVA) | |||
|---|---|---|---|---|---|---|---|
| Control group M ± SD | Experimental group M ± SD | ||||||
| T | p | ||||||
| Desire | Baseline | 6 | 3.50 ± .90 | 3.30 ± 1.16 | 2.691 | .009* | F = 12.333 p-value = .001* |
| After Kegel exercise training | 3.12 ± 1.03 | 3.92 ± 1.11 | |||||
| Arousal | Baseline | 6 | 3.64 ± 1.06 | 3.61 ± 1.19 | 2.908 | .005* | |
| After Kegel exercise training | 3.18 ± .87 | 4.08 ± 1.22 | |||||
| The female sexual function index (FSFI) | Baseline | 12 | 7.14 ± 1.72 | 6.91 ± 1.97 | 3.168 | .002* | |
| After Kegel exercise training | 6.30 ± 1.74 | 8.00 ± 2.21 | |||||
Univariate analysis of variance (ANCOVA) and independent samples t-test for FSFI domains in both groups (control and experimental).
Descriptive statistics, t, t-test; F, ANCOVA.
Significant at p ≤ 0.05.
Table 7 presents the mean values of the pain scales at baseline and after intervention in both groups. T-test illustrated that there were statistically significant differences between control and experimental groups after intervention in the Visual Analog Scale (VAS) and Faces Pain Rating Scale at p < 0.05. Also, the t-test showed a significant decrease for the experimental group after the Kegel exercise intervention in both subscales (2.40 ± 2.16 &83 ± 1.02). ANCOVA showed that the differences between the control and experimental groups were statistically significant in the Visual Analog Scale (VAS) and Faces Pain Rating Scale at p < 0.05 [F = 6.786 (012*), F = 10.673(002*)], respectively (Table 7).
Table 7
| Variables | Group | Significance test independent samples t-test | Univariate analysis of variance (ANCOVA) | |||
|---|---|---|---|---|---|---|
| Control group n.31 | Experimental group n.30 | |||||
| M ± SD | M ± SD | T | Sig. | |||
| The visual analog scale (VAS) | Baseline | 4.26 ± 2.95 | 5.70 ± 2.81 | 3.302 | .002* | F = 6.786 p-value = .012* |
| After Kegel exercise training | 3.61 ± 2.50 | 2.40 ± 2.16 | ||||
| Faces pain rating scale | Baseline | 2.10 ± 1.42 | 2.20 ± 1.37 | 2.557 | .013* | F = 10.673 p-value = .002* |
| After Kegel exercise training | 1.81 ± 1.35 | .83 ± 1.02 | ||||
Univariate analysis of variance (ANCOVA) and independent samples t-test for pain scales in both groups (control and experimental).
Descriptive statistics, t, t-test; F, ANCOVA.
Significant at p ≤ 0.05.
Table 8 represents the mean values of all measured variables at baseline and after the Kegel exercise training intervention in both groups. MANOVA showed a significant increase in FSFI in the experimental group after the intervention, with the mean value for the experimental group at baseline being (6.91 ± 1.97) and after (8.00 ± 2.21) at p = 0.002. Also, the table illustrates a significant decrease in the Visual Analog Scale and Faces Pain Rating Scale in both groups after the Kegel exercise training intervention at p = 0.002 (Table 8).
Table 8
| Domains | Maximum allowed score | Groups | F-value | Intervention-time interaction p-value | |||
|---|---|---|---|---|---|---|---|
| Control group n.31 | Experimental group n.30 | ||||||
| M ± SD | Min-max | M ± SD | Min-max | ||||
| Pelvic floor disability index (PFDI-20) | |||||||
| Baseline | 300 | 67.37 ± 60.14 | .00–219.79 | 76.18 ± 66.70 | .00–251.04 | 3.405 | .070 |
| After Kegel exercise training | 81.82 ± 59.81 | .00–225.00 | 54.34 ± 74.23 | .00–300.00 | |||
| The female sexual function index (FSFI) | |||||||
| Baseline | 12 | 7.14 ± 1.72 | 2.70–10.20 | 6.91 ± 1.97 | 1.80–10.80 | 10.039 | .002* |
| After Kegel exercise training | 6.30 ± 1.74 | 1.50–9.00 | 8.00 ± 2.21 | 2.40–10.80 | |||
| The visual analog scale | |||||||
| Baseline | 10 | 4.26 ± 2.95 | 1.00–10.00 | 5.70 ± 2.81 | 1.00–10.00 | 10.905 | .002* |
| After Kegel exercise training | 3.61 ± 2.50 | 1.00–10.00 | 2.40 ± 2.16 | 1.00–10.00 | |||
| Faces pain rating scale | |||||||
| Baseline | 5 | 2.10 ± 1.42 | .00–5.00 | 2.20 ± 1.37 | .00–5.00 | 6.540 | .013* |
| After Kegel exercise training | 1.81 ± 1.35 | .00–4.00 | .83 ± 1.02 | .00–3.00 | |||
Repeated measures MANOVA for all measured variables in both groups (control and experimental).
Descriptive statistics, t, t-test, F, MANOVA.
Significant at p ≤ 0.05.
The change between groups corresponded to a high effect size in the Visual Analog Scale, the Female Sexual Function Index, and Faces Pain Rating Scale (Cohen d = 0.84, 0.81, and 0.65, respectively), and a moderate effect size in the Pelvic Floor Disability Index in favor of the experimental group (Table 8).
Table 9 shows Cohen's d effect sizes for the Kegel exercise intervention. The intervention had a medium effect on pelvic floor function (PFDI-20, d = 0.473) and medium-to-large effects on pain reduction (VAS, d = 0.846; Faces Pain Scale, d = 0.655). The strongest impact was on sexual function (FSFI, d = 0.811, large effect). Overall, the intervention meaningfully improved pelvic floor health, sexual function, and pain outcomes.
Table 9
| Scales | Cohen's d |
|---|---|
| Pelvic floor disability index (PFDI-20) | .473 |
| The female sexual function index (FSFI) | .811 |
| The visual analog scale (VAS) | .846 |
| Faces pain rating scale | .655 |
Independent samples effect sizes of the Kegel exercise intervention among study groups (control and experimental).
Cohen's d: a standardized effect size.
A Pearson's Correlation was run to determine the relationship between pre- and post-tests for the four domains (PFDI-20, FSFI, The Visual Analog Scale, and Faces Pain Rating Scale) and participants’ demographic data. There was a positive correlation between PFDI-20 at baseline and women's age, which was statistically significant (r = .254*, p = .048). Also, the results revealed that the FSFI was negatively correlated with women's marital status and monthly income at baseline [r = −.264* (040) and r = −.317* (.013) respectively] and positively correlated with women's place of residence after intervention [r = .260* (.043)] (Table 10).
Table 10
| Domains | Age n.61 | Marital status n.61 | Education n.61 | Working condition n.61 | Monthly income n.61 | Place of residence n.61 | |
|---|---|---|---|---|---|---|---|
| Pelvic floor disability index (PFDI-20) | |||||||
| Baseline | r (p-value) | .254* (.048) | −.114 (.383) | .028 (.828) | −.159 (.220) | .106 (.416) | −.070 (.589) |
| After Kegel exercise training | r (p-value) | −.118 (.364) | −.130 (.316) | −.014 (.915) | .002 (.989) | .035 (.791) | −.212 (.101) |
| The female sexual function index (FSFI) | |||||||
| Baseline | r (p-value) | −.174 (.180) | −.264* (.040) | .037 (.774) | .045 (.728) | −.317* (.013) | −.077 (.553) |
| After Kegel exercise training | r (p-value) | .052 (.693) | .186 (.152) | .021 (.874) | −.045 (.732) | −.038 (.770) | .260* (.043) |
| The visual analog scale | |||||||
| Baseline | r (p-value) | .056 (.667) | −.087 (.506) | −.142 (.275) | .202 (.119) | −.089 (.494) | −.044 (.735) |
| After Kegel exercise training | r (p-value) | −.157 (.227) | −.109 (.401) | −.074 (.568) | .171 (.188) | −.045 (.730) | −.149 (.253) |
| Faces pain rating scale | |||||||
| Baseline | r (p-value) | .020 (.881) | −.014 (.916) | −.062 (.633) | .122 (.351) | −.031 (.810) | −.098 (.452) |
| After Kegel exercise training | r (p-value) | −.161 (.217) | −.134 (.302) | .046 (.724) | .025 (.846) | −.003 (.981) | .030 (.819) |
Correlation between sociodemographic data and pre- and post-tests for the four domains.
Pearson's Correlation: r: Correlation coefficient, p-value: Sig. (2-tailed).
Significant at p ≤ 0.05.
A Pearson's Correlation was also run to determine the relationship between participants’ previous pregnancy history and pre- and post-tests for the four domains. No statistically significant correlations were found in this study between previous pregnancy history and pre- and post-tests for the four domains (Table 11).
Table 11
| Domains | Miscarriage n.61 | Type of delivery n.61 | Number of children n.61 | |
|---|---|---|---|---|
| Pelvic floor disability index (PFDI-20) | ||||
| Baseline | r (p-value) | .159 (.221) | .088 (.501) | .001 (.993) |
| After Kegel exercise training | r (p-value) | .072 (.583) | −.151 (.245) | −.096 (.464) |
| The female sexual function index (FSFI) | ||||
| Baseline | r (p-value) | −.014 (.917) | −.218 (.091) | −.061 (.642) |
| After Kegel exercise training | r (p-value) | −.009 (.944) | .160 (.218) | −.104 (.423) |
| The visual analog scale | ||||
| Baseline | r (p-value) | .072 (.582) | −.164 (.208) | −.080 (.540) |
| After Kegel exercise training | r (p-value) | .108 (.409) | −.194 (.134) | −.158 (.224) |
| Faces PAIN RATING SCALe | ||||
| Baseline | r (p-value) | .003 (.981) | −.113 (.386) | −.080 (.540) |
| After Kegel exercise training | r (p-value) | .010 (.939) | −.127 (.329) | −.198 (.127) |
Correlation between participants’ previous pregnancy history and pre and post-tests for the four domains.
Pearson's correlation: r: correlation coefficient, p-value: Sig. (2-tailed).
Discussion
Kegel exercise, also called pelvic floor exercises (PFEs) or pelvic muscle strengthening exercises, is defined as repetitive contractions of the pelvic muscles that control the flow in urination to strengthen these muscles, especially to control or prevent incontinence or to enhance sexual responsiveness during intercourse (
The current study's main findings demonstrated that following the Kegel exercise training intervention, the Visual Analog Scale (VAS) and Face Pain Rating Scale significantly decreased in both the control and experimental groups, with the experimental group having significantly lower scores (2.40 ± 2.16,.83 ± 1.02, respectively). The pelvic floor muscles can undergo natural rehabilitation after delivery (
Furthermore, previous research showed that pelvic floor muscle training activities could help manage pelvic floor dysfunction. In a randomized controlled experiment, Johannessen et al. (2020) found that frequent pelvic floor muscle training reduced urine incontinence three months postpartum (42). Woodley et al. also found that pelvic floor muscle training can improve urine and fecal incontinence in prenatal and postnatal women (
In addition, this study found that the Pelvic Floor Disability Index at baseline was positively correlated with increasing age in women. Age-related decline in pelvic floor muscle function has been linked to an increase in the incidence of pelvic floor disorders.
Based on the results of this study, female sexual function index (FSFI) scores were significantly increased in the experimental group across all domains after the Kegel exercise training intervention. Hadizadeh-Talasaz et al. (
The levator ani muscle is a broad, thin muscle group situated on either side of the pelvis. It is strengthened through muscular hypertrophy during Kegel exercises, which enhances support (
Limitations
The present study has several limitations that warrant consideration. It relied on a convenience sample of multiparous women who delivered vaginally, and the relatively small sample size and single-center design may limit the generalizability of the findings to the broader Saudi Arabian population. Cultural factors, including modesty and discomfort in discussing sexual health, could have influenced participants’ responses, despite efforts to foster a supportive and welcoming environment.
Due to cultural sensitivity, participant discomfort, and limited availability of trained assessors, manual muscle testing and vaginal examinations were not feasible; hence, validated functional outcome measures (PFDI-20) were employed as indirect indicators of pelvic floor muscle performance. While pelvic floor rehabilitation may require longer intervention periods, a 6-week intervention was chosen based on feasibility and evidence from prior studies demonstrating short-term benefits in postpartum women. Nevertheless, the lack of long-term follow-up constrains conclusions regarding the sustainability of outcomes, highlighting the need for future research with extended monitoring. Adherence was assessed via self-report, which may introduce bias; subsequent studies are encouraged to implement objective adherence tracking to enhance reliability.
Despite these limitations, the findings provide preliminary but robust evidence supporting the effectiveness of structured health education on Kegel exercises in improving pelvic floor function, alleviating pain, and enhancing sexual function among postpartum women.
Conclusion
Regarding the impact of Kegel exercise on maternal postpartum pain, pelvic floor dysfunction, and sexual function, the findings of this study showed that female sexual function index (FSFI) scores were significantly increased after the Kegel exercise training intervention. Following the Kegel exercise training intervention, there was a significant decrease in the Visual Analog and Faces Pain Rating Scales. Therefore, the study's null hypothesis is rejected. There were, however, no statistical differences in the total score of pelvic floor dysfunction after the intervention.
Recommendations
Kegel exercises, which target the pelvic floor muscles and have been shown to strengthen them after pregnancy and childbirth, should be considered a viable treatment option that can be introduced into the clinical and counseling services provided to mothers in Saudi Arabia. Hospital policies should be put in place to establish and maintain pelvic floor exercise training programs that would afford women the opportunity to engage in these exercises before and after pregnancy.
Nurse midwives can also promote a standard of care and practice where changes in the body during pregnancy and after birth are addressed through education, training, treatment, and self-care to decrease problems caused by pelvic floor muscle relaxation following vaginal delivery, improve women's sexual function, and reduce postpartum pain. To aid in the early prevention of pelvic floor disorders in women, nurse midwives should encourage women to improve the frequency and consistency of pelvic floor exercises following delivery. More training for midwives on how to teach the mother the Kegel exercise.
As the intervention of this study was limited to 6 weeks, further research should be carried out to assess the effects of Kegel exercise over a longer period of time and across a more diverse population and parameters.
Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Ethics statement
The studies involving humans were approved by Institutional Review Board (IRB) at King Abdul-Aziz Medical City-Western Region and the College of Nursing Research Unit of the King Abdullah International Medical Research Center (KAIMRC) [IRB/1251/22, study number SP22J/060/05]. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
JA: Supervision, Methodology, Validation, Investigation, Writing – review & editing, Data curation, Conceptualization, Visualization, Software, Writing – original draft, Formal analysis, Resources, Funding acquisition, Project administration. NA: Validation, Conceptualization, Funding acquisition, Investigation, Visualization, Writing – review & editing, Resources, Writing – original draft, Supervision, Project administration, Methodology, Data curation, Software, Formal analysis. NH: Methodology, Data curation, Visualization, Project administration, Conceptualization, Validation, Supervision, Funding acquisition, Software, Investigation, Formal analysis, Writing – review & editing, Writing – original draft, Resources.
Funding
The author(s) declared that financial support was received for this work and/or its publication. The authors declare that this study was financially supported by the Saudi National Institute for Health (SNIH) [Project No. 37764054, dated 1/8/2023].
Acknowledgments
The researcher extends sincere appreciation to all participants, particularly the women, for their time and valuable contributions to this study. Gratitude is also expressed to the SNIH for their financial support throughout the study.
Conflict of interest
The author(s) declared that this work 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) declared that generative AI was used in the creation of this manuscript. During the preparation of this work, the authors used ChatGPT to improve the manuscript's readability and language. After using this tool, the authors reviewed and edited the content as needed and took full responsibility for the final version of the manuscript.
Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
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.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/frph.2026.1746383/full#supplementary-material
Abbreviations
Abbreviations CADI, colorectal-anal distress inventory; FSFI, female sexual function index; IRB, institutional review board; IBM, international business machine; PFDI, pelvic floor disability index; PFD, pelvic floor dysfunction; SNIH, Saudi National Institute for Health; SPSS, statistical package for social sciences; UDI, urinary distress inventory; VAS, visual analog scale; WHO, World Health Organization.
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Summary
Keywords
Kegel exercise, pelvic floor dysfunction, postpartum complications, postpartum pain, sexual function
Citation
Alharbi JH, Abdul Manan NI and Hantira NY (2026) Empowering postpartum women through health education on Kegel exercises: effects on pain, pelvic floor dysfunction, and sexual function. Front. Reprod. Health 8:1746383. doi: 10.3389/frph.2026.1746383
Received
14 November 2025
Revised
04 January 2026
Accepted
12 January 2026
Published
02 February 2026
Volume
8 - 2026
Edited by
Jieyun Yin, Soochow University, China
Reviewed by
Andrea Chisari, Azienda Sanitaria Provinciale di Catania, Italy
Gehan A. Abdelsamea, Cairo University, Egypt
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Copyright
© 2026 Alharbi, Abdul Manan and Hantira.
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: Neama Y. Hantira dr.neamayousef@gmail.com
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.