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临床试验/NCT07156266
NCT07156266已完成不适用

Comparative Effects of Kegal and Squat Exercises on Urinary Incontinence Severity and Quality of Life

University of Faisalabad1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年2月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
Urinary incontinence

研究概览

简要总结

A randomized clinical trial will be carried out to compare the effectiveness of Kegel and squat exercises in reducing urinary incontinence. The study will include 30 participants diagnosed with urinary incontinence, who will be randomly assigned to either a Kegel exercise group or a squat exercise group. Both groups will perform their respective exercises for 10 minutes, three times daily, over a period of 12 weeks. Outcomes will be assessed using the International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms Long Form (ICIQ-FLUTS LF) and the Incontinence Quality of Life (I-QOL) questionnaire

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
30 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Women aged between 30 and 60 years with a confirmed diagnosis of urinary incontinence (UI) by a qualified healthcare professional.
  • •Women who are physically able to perform the required exercises and are willing to provide informed consent to participate in the study.

排除标准

  • •Pregnant women or those planning to become pregnant during the study period. Individuals who have undergone surgery within the past six months that may affect pelvic floor strength or urinary incontinence symptoms.
  • •Women with neurological disorders, current urinary tract infections (UTIs), or a history of recurrent UTIs that could influence pelvic floor function or UI symptoms.

研究组 & 干预措施

Group A (Kegal Exercise Group)

Experimental

干预措施: Kegal Exercise (Procedure)

Group B (Squats Exercise Group)

Active Comparator

干预措施: Squats Exercise (Procedure)

结局指标

主要结局

Urinary incontinence

时间窗: 12 weeks

The International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms Long Form (ICIQ-FLUTS-LF) will be used to assess the severity of urinary incontinence.

次要结局

  • The Incontinence Quality of Life(12 Weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Izza Ayub; PT

Lecturer

University of Faisalabad

研究点 (1)

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