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Abdominal-Kegel Exercise and the Effect of Telemedicine in Stress Urinary Incontinence

Stress Urinary Incontinence Clinical Trial

Official title:
Abdominal-Kegel Exercise in Patients With Stress Urinary Incontinence and the Effect of Telemedicine Applications on Adaptation to Lifestyle Changes: A Randomized Controlled Study

Clinical Trial Summary

Urinary incontinence is a very common health problem that reduces the quality of life mostly in women. Behavioral therapy (lifestyle changes, abdominal-Kegel exercises) is recommended as the first choice in the treatment of the disease. It is known that surgical and medical treatment cannot give a definite result. The application of behavioral therapy with telemedicine has advantages such as reducing the cost and increasing the treatment rate. In this study, it is aimed to evaluate the effect of telemedicine practices on compliance with multi-module behavioral therapy in women with stress urinary incontinence.

Clinical Trial Description

The study is a randomized controlled study to be conducted in female patients between the ages of 20-65 who applied to the Eskişehir City Hospital urology outpatient clinic and diagnosed with stress urinary incontinence. When type 1 (α) error was 5%, type 2 error (1-β) was 95%, and the effect size was accepted as 0.5, it was calculated that there should be at least 47 people in the groups. Stratified and block randomization will be used to recruit patients into study groups. The patients will be evaluated with the QUID test, risk assessment questionnaire in patients with stress urinary incontinence, incontinence short test, bladder diary, daily urinary incontinence, a notebook to record the duration of the exercises to be performed, quality of life scale and lifestyle changes questioning form. The intervention group will be re-evaluated as a result of the intervention with measurement tools. Intervention group: Brochure about incontinence will be given, web-based training will be applied, SMS will be sent every day according to the risks. Control group: Only brochure will be given. It is expected that a low-cost application to be developed after the study will reduce the complaints of the patients, increase their quality of life and have a positive effect on women's health. It is difficult for physicians to allocate sufficient time to convey lifestyle changes and exercises to patients with stress urinary incontinence during their busy work hours in the clinic. After the success to be achieved, the usage rate of the website to be prepared will be increased through various scientific platforms and associations. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06189443
Study type Interventional
Source Eskisehir Osmangazi University
Contact
Status Enrolling by invitation
Phase N/A
Start date January 1, 2023
Completion date July 30, 2024
View Details
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