Ireland
--:--IST
Recruiting Not applicable

Effects of Action Observation and Metaphorical Imagery in Pelvic Floor Muscle Training for Geriatric Urinary Incontinence

NCT07551674 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-03-19
Last updated
2026-05-11

Condition(s) studied

Urinary Continence

Investigational drug(s) / intervention(s)

Pelvic Floor Muscle Training programPelvic Floor Muscle Training via Action Observation Therapy

Pelvic Floor Muscle Training program: Participants will engage in a 12-week Pelvic Floor Muscle Training (PFMT) program. The exercises will be conducted twice a week in group sessions lasting 45-50 minutes each. These sessions will be supervised by a physiotherapist and performed in small groups of five participants.

Pelvic Floor Muscle Training via Action Observation Therapy: Participants will be enrolled in a Pelvic Floor Muscle Training (PFMT) program using the action observation method accompanied by metaphorical imagery. This program will be administered over 12 weeks, consisting of twice-weekly group sessions lasting 45-50 minutes each. The exercise content is identical for both groups. However, during the sessions for this specific group, metaphor-themed visuals will be projected onto a screen, and participants will be given the instruction: 'Perform the movement by imagining it as shown in the visual.' To enhance physical participation and motivation, verbal cues and positive reinforcement will be provided by the physiotherapist. The exercises and the corresponding metaphors will be updated on a weekly basis. All sessions will be supervised by a physiotherapist in small groups of five participants.

Study summary

This clinical trial investigates the effects of a 12-week Pelvic Floor Muscle Training (PFMT) program applied via Action Observation Therapy (AOT) with metaphorical imagery on urinary incontinence, quality of life, and treatment adherence in geriatric women. The study will be conducted between June 2025 and June 2026 in nursing homes in Istanbul, targeting women aged 65 and older who are diagnosed with stress or stress-predominant mixed urinary incontinence, possess normal cognitive function (Standardized Mini Mental Test score ≥ 24), and walk independently. Eligible participants will be divided into groups, where both will undergo a progressive exercise regimen involving twice-weekly 45-50 minute group sessions that advance from supine positions to standing and jumping movements. However, the AOT study group will uniquely perform these exercises while observing and imagining projected metaphor-themed visuals to enhance motor learning and motivation. Efficacy will be evaluated pre- and post-intervention using various standardized tools, including the Pelvic Floor Distress Inventory-20, a 24-hour pad test, the Incontinence Severity Index, the Movement Imagery Questionnaire-3, and the Incontinence Quality of Life Scale, to comprehensively assess improvements in incontinence severity, functional status, and overall well-being.

Eligibility

Sex
FEMALE
Min age
65 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with stress or stress-predominant mixed urinary incontinence by a physician * Women aged 65 years and older * Literate in Turkish to understand, interpret, and answer the questionnaires * Scoring 24 or higher on the Mini-Mental State Examination (MMSE) * Able to walk independently without the use of any walking aids (assistive devices) * Having signed the informed consent form Exclusion Criteria: * Received pelvic floor muscle training within the past 6 months * Presence of fecal incontinence * Current genitourinary infection or use of medication for urinary incontinence * History of urinary incontinence surgery or presence of symptomatic pelvic organ prolapse * Presence of neurological, orthopedic, psychiatric, hematological, or cardiovascular conditions that would preclude participation in exercise * Body mass index (BMI) ≥ 25 kg/m² * Hearing or visual impairments that would negatively affect participation * Presence of hematuria, urethral and/or bladder fistula, or a history of pelvic surgery

Primary outcome measure(s)

  • Mini-Mental State Examination — Baseline and after 12-weeks
  • Pelvic Floor Distress Inventory — Baseline and after 12-weeks
  • The Incontinence Severity Index — Baseline and after 12-weeks
  • Movement Imagery Questionnaire-3 — Baseline and after 12-weeks

Trial sites (1)

FacilityCityRegionStatus
Fenerbahce University Department of Physiotherapy and Rehabilitation Istanbul Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07551674 on ClinicalTrials.gov ↗ ← All trials in Turkey