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Effectiveness of Yoga and Pilates Training for Urinary Incontinence in Elderly Women: A Clinical Trial

Effectiveness of Yoga and Pilates Compared with Standard Care for Urinary Incontinence in Elderly Women: A Randomised Controlled Pilot Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000784112
Enrollment
30
Registered
2019-05-27
Start date
2019-05-31
Completion date
Unknown
Last updated
2019-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The purpose of the clinical trial is to assess the effectiveness of Yoga and Pilates compared with standard care on urinary incontinence among elderly women. A total of 30 participants will be divided into to three groups of 10 to receive either Yoga or Pilates or Standard Care once a week for 4 weeks provided by the respective trained professionals in the form of group classes in an elderly centre. All study participants will be required to perform CD-guided home exercises for 8 weeks without trainers’ supervision after the 4-week training. The study will determine the effectiveness of Yoga and Pilates in reducing the symptoms of stress urinary incontinence among elderly women, for example the amount and frequency of involuntary leaks of urine during coughing, sneezing and physical exertion, compared with standard care.

Interventions

An assessor-blinded, prospective, three-arm parallel group randomized controlled pilot trial will be conducted over a period of 12 weeks with elderly women (n = 30) presenting with symptoms of stress or mixed urinary incontinence. The three intervention groups include Pilates (n = 10), Yoga (n = 10) and Standard Care as an active control group (n = 10). "Arm 1: Standard Care" For participants assigned to standard care group (n = 10), pelvic floor muscle training (PFMT) will be provided by a ce

An assessor-blinded, prospective, three-arm parallel group randomized controlled pilot trial will be conducted over a period of 12 weeks with elderly women (n = 30) presenting with symptoms of stress or mixed urinary incontinence. The three intervention groups include Pilates (n = 10), Yoga (n = 10) and Standard Care as an active control group (n = 10). "Arm 1: Standard Care" For participants assigned to standard care group (n = 10), pelvic floor muscle training (PFMT) will be provided by a certified perineal therapist. The trainer will provide the intervention once a week for 4 weeks, with each session lasting 45 minutes to one hour, in the form of group classes to a group of 10 in an elderly centre in Hong Kong. At the end of this 4-week training, all participants will receive a CD with videos taken when the trainer conducts her sessions at the centre. All study participants will be required to perform CD-guided unsupervised home exercises 3 to 6 times per week for 8 weeks. Each of the home exercise sessions last 30 to 45 minutes. PFMT will first be taught in a position in which gravity is eliminated (lying) and will gradually progress to positions in which gravity is partially eliminated, followed by movements that are against gravity. The procedures of PFMT are as follows: Step 1: women will be asked to contract their pelvic floor muscles (urethra) and hold the contraction for 3-6 seconds, then relax for another 10 seconds. Step 2: women will be asked to control the bowel action (or control passage of wind), hold it for 3-6 seconds and then relax for another 10 seconds. Step 3: women will be asked to contract their urethral orifice and control bowel action, draw the vagina up and hold it for 3-6 seconds and then relax for another 10 seconds. This exercise will improve the strength of the entire pubococcygeus muscle i.e., the pelvic floor muscles. "Arm 2: Pilates" For participants assigned to Pilates group (n = 10), Pilates training will be provided by a Pilates trainer once a week for 4 weeks, with each session lasting 45 minutes to one hour, in the form of group classes to a group of 10 in an elderly centre in Hong Kong. At the end of this 4-week training, all participants will receive a CD with videos taken when the trainer conducts her sessions at the centre. All study participants will be required to perform CD-guided unsupervised home exercises 3 to 6 times per week for 8 weeks. Each of the home exercise sessions last 30 to 45 minutes. Pilates will first be taught in a position in which gravity is eliminated (lying) and will gradually progress to positions in which gravity is partially eliminated, followed by movements that are against gravity. Warm-up exercises for Pilates will include: roll down, leg springs, walking, frog, circles, single leg stretch, scissors, lower and lift, spine stretch, swan prep, and crisscross. Pilates training will include: Pilates breathing, neutral pelvis, knee folds, knee sways, heel slides, elevator, pelvic clock, pelvic rocks, coccyx curl, pelvic lift, bridging, and abdominal stabilization. "Arm 3: Yoga" For participants assigned to Yoga group (n = 10), Yoga will be provided by a certificated Yoga trainer with 500 hours of Yoga training in the Yoga school. The trainer will provide the intervention once a week for 4 weeks, with each session lasting one hour, in the form of group classes to a group of 10 in an elderly centre in Hong Kong. At the end of this 4-week training, all participants will receive a CD with videos taken when the trainer conducts her sessions at the centre. All study participants will be required to perform CD-guided unsupervised home exercises 3 to 6 times per week for 8 weeks. Each of the home exercise sessions last 30 to 45 minutes. The yoga postures used are as follows: Hatha yoga styles, which include 8 postures, will be performed: Tadasana, Utkatasana, Trikonasana, Malasana, Viparita Karani Variation, Salamba Set Bandhasana, Supta Baddha Konasana, and Savasana. "Adherence to Schedules" Researchers will telephone each patient every week to ensure patients’ adherence to schedules over the period of 8 weeks of CD-guided unsupervised home exercises.

Sponsors

Priya Kannan
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Women aged 60 or above 2. Women presenting with symptoms of stress urinary incontinence at a bladder volume 200 to 250 ml (involuntary loss of urine on effort or physical exertion, or on sneezing or coughing), or mixed urinary incontinence (stress and urgency incontinence) 3. International Consultation on Incontinence Questionnaire for Urinary Incontinence Short Form (ICIQ-UI-SF) at least 6 points (out of 21) 4. Provision of written informed consent

Exclusion criteria

1. Women having pure urgency urinary incontinence 2. Women having urinary incontinence caused by other diseases, such as Parkinson’s Disease, multiple sclerosis, spinal cord injury or Alzheimer’s disease. 3. Women having cognitive impairment (Mini-Mental State Examination [MMSE] score < 23) that affects their capacity to give informed consent 4. Women who have been diagnosed Stage 3 or 4 pelvic organ prolapse according to Pelvic Organ Prolapse Quantification System 5. Women who have been diagnosed, and currently having treatment for pelvic cancer 6. Women who have urinary tract infection or haematuria 7. Women who suspected urethral and/or vesical fistula 8. Women who are bedridden 9. Women who are currently participating in other research relating to urinary incontinence

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026