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临床试验/NCT00178282
NCT00178282终止不适用

Pilot Study: Low Intensity Physical Therapy for Prevention of Pre and Postpartum Urinary Incontinence

University of Rochester2 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2005年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
23
试验地点
2
主要终点
Non-intensive physical therapy, 24hr. voiding diary, pad weight, Quality of Life questionnaires

研究概览

简要总结

The purpose of this study is to determine if pelvic exercises can reduce the occurrence of urinary incontinence (involuntary loss of urine) before and after delivery. We would also like to see if performing pelvic exercises before birth has an effect on labor and/or delivery, and if there are any specific characteristics for developing urinary incontinence during pregnancy and after delivery.

详细描述

The studies investigating physiotherapy for prevention of urinary incontinence during and after pregnancy used intensive pelvic floor muscle training. While physical therapy appears to be effective in preventing urinary incontinence, extensive physical therapy is too costly to be implemented as a preventive measure for the general population. Thus, we want to asses if non-intensive pelvic floor therapy decreases the urinary incidence of incontinence during pregnancy and postpartum. We propose a prospective randomized controlled trial to obtain baseline data on the effect of non-intensive pelvic floor muscle training of urinary incontinence in primigravid women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Nulliparous, pregnant women, 18 years or older
  • Less than 20 weeks gestation
  • Able to give consent and who are willing to participate

排除标准

  • Multiparous women
  • Women presenting after 20 weeks gestation
  • History of urinary incontinence
  • Mentally impaired women and women who have neurological impairment affecting ability to perform pelvic floor muscle training

结局指标

主要结局

Non-intensive physical therapy, 24hr. voiding diary, pad weight, Quality of Life questionnaires

时间窗: During and 3 months after delivery

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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