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临床试验/NCT06537544
NCT06537544已完成不适用

Comparison of Comprehensive Rehabilitation Program and Conventional Pelvic Floor Training in Women With Stress Urinary Incontinence

Riphah International University2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
2
主要终点
Severity of stress urinary incontinence

研究概览

简要总结

The goal of this clinical trial is to compare a comprehensive rehabilitation program and a conventional pelvic floor training program in women with stress urinary incontinence,to compare the effects of comprehensive rehabilitation program and conventional pelvic floor training on the severity of SUI, on the strength of pelvic floor muscle and on quality of life in women with SUI. Following the randomization into either the conventional pelvic floor training or comprehensive rehabilitation program group, participants will receive their assigned interventions of three weekly sessions for eight weeks.

详细描述

The proposed study comparing the effects of conventional pelvic floor training versus a comprehensive rehabilitation program on stress urinary incontinence (SUI) among perimenopausal women holds significant rationale and importance. Given the prevalence and impact of SUI on the quality of life of perimenopausal women, investigating the comparative efficacy of these interventions is crucial for informing evidence-based clinical practice. The study aims to provide insights into the most effective management strategies for SUI in this population, potentially leading to improved treatment outcomes, enhanced quality of life, and reduced healthcare burden associated with this common condition. By addressing this research gap, the study has the potential to significantly benefit both individual patients and the broader healthcare system.

This will be a randomized controlled trial. Non probability sampling technique will be used.The data collection procedure begins with the recruitment phase, potential participants meeting the study's criteria will be identified and provided with detailed information about the research aims and procedures. Once recruited, participants will undergo a screening process to confirm their eligibility, including assessments such as medical history reviews and diagnostic tests. After obtaining informed consent, baseline assessments will be conducted to establish the participants' initial status regarding urinary symptoms and quality of life. Following randomization into either the conventional pelvic floor training or comprehensive rehabilitation program group, participants will receive their assigned interventions of three weekly sessions for eight weeks.

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
40 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Perimenopausal and post-menopausal women
  • Age 40-60 years
  • Medically diagnosed patients of stress urinary incontinence

排除标准

  • History of pelvic surgery within the past six months.
  • Current urinary tract infections or other active urinary tract disorders.
  • Neurological conditions affecting bladder control.
  • Inability to participate in the prescribed intervention due to physical or cognitive limitations.
  • Participation in other pelvic floor rehabilitation programs concurrently or previously within the last 6 months.

结局指标

主要结局

Severity of stress urinary incontinence

时间窗: Changes from Baseline to 8 weeks

To compare the effects of comprehensive rehabilitation program and conventional pelvic floor training on the severity of stress urinary incontinence

次要结局

  • Strength of pelvic floor muscle(Changes from Baseline to 8 weeks)
  • Quality of life in women with stress urinary incontinence(Changes from Baseline to 8 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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