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Kegel Exercises for Stress Urinary Incontinence

Not Applicable
Completed
Conditions
Urinary Incontinence,Stress
Interventions
Behavioral: biofeedback training
Registration Number
NCT05529238
Lead Sponsor
Charles Darwin University
Brief Summary

Study about a targeted group of women suffering from self-reported stress urinary incontinence, attend a Kegel exercise training program. The group was divided into two; supervised and unsupervised. Whilst both groups benefited from initially seeing a women's health physiotherapist for a pelvic floor muscle assessment and a bespoke Kegel exercise program, only the supervised group continued to see the physiotherapist for monthly bio-feedback training. The unsupervised group relied on their own motivation to perform their Kegel exercises as prescribed. At the end of the twelve week program, both groups had a final pelvic floor muscle strength assessment by the physiotherapist to determine any changes and subsequent improvements in urinary incontinence.

Aim : Investigate and compare the efficacy of supervised Kegel exercises with biofeedback on Stress Urinary Incontinence (SUI) and Pelvic Floor Muscle Strength (PFMS) compared to unsupervised Kegel exercises.

The primary goal of this study was to determine the effectiveness of supervised Kegel exercises using BT versus unsupervised Kegel exercises without biofeedback training, on SUI. A secondary outcome was to establish whether an improvement was observed in PFMS and subsequently, the effect of this on SUI. It was hypothesized that regular support and visual motivation and direction of BT from the physiotherapist, would provide greater results.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
29
Inclusion Criteria
  • being female
  • aged over 18 years
  • suffer from SUI (their subjective disclosure was based on a description provided for their reference)
  • did not perform Kegel exercises
  • be available for duration of 12-week program
Exclusion Criteria
  • pregnancy and breastfeeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
supervised group during studybiofeedback trainingmonthly physiotherapist appointment for half of the cohort including pelvic floor examination by physiotherapist including digital palpation and perineometry.
Primary Outcome Measures
NameTimeMethod
Incontinence severity (ISI) index toolWeek 12

self-reported questionnaire describing frequency/severity of urinary incontinence. the higher the number, the higher the impact.

Pelvic floor assessment from physiotherapistweek 12

pelvic floor muscle strength

Incontinence severity index (ISI) toolWeek 0

self-reported questionnaire describing frequency/severity of urinary incontinence. the higher the number, the higher the impact.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Charles Darwin University

🇦🇺

Darwin, Northern Territory, Australia

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