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临床试验/NCT01599715
NCT01599715已完成2 期

Translating Unique Learning for Incontinence Prevention for Women Over the Age of 55

University of Michigan2 个研究点 分布在 1 个国家目标入组 647 人开始时间: 2010年9月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
647
试验地点
2
主要终点
Translating Unique Learning for Incontinence Prevention (TULIP)

研究概览

简要总结

More than one in three US women suffers from the distressing, embarrassing, and often unreported problem of urinary incontinence (UI). UI severity increases with age and the financial cost exceeds $19 billion per year . The Adult Conservative Management Committee of the 2008 International Consultation on Incontinence concluded that pelvic floor muscle training (PFMT) should be offered as first line therapy to all women with stress, urge, or mixed UI; and that bladder training (BT) may be preferred to drug therapy. Conservative strategies are low risk and differ from other forms of UI management in that they do not prejudice future treatments. They also may decrease symptoms of urgency and frequency that do not entail UI, but greatly reduce the quality of life for nearly 1 in 11 US women.

详细描述

The study will attempt to accomplish 3 aims:

Aim 1: Compare outcomes of the two-hour BH Class with the condensed DVD version.

To accomplish this aim we will conduct a comparative effectiveness trial of 600 women 55 years and older randomized to BH Class or DVD. Women will be followed for 24 months post-intervention in order to assess long-term outcomes and sustainability.

Aim 2: Conduct an economic analysis comparing the two-hour BH Class with the DVD version. Describing the costs, quality of life, and analyzing the willingness to pay and employment/ productivity data will be the primary economic focus of this study.

Aim 3: Conduct a qualitative analysis to gain insight into elements of the intervention that contribute to sustainability.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
Single (Investigator)

入排标准

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

入选标准

  • •Female, aged 55 years or older
  • •An additive sum of the frequency (question 1) and volume (question 2) items from the International Consultation on Incontinence Questionnaire-Short Form is ≤5
  • •Negative for demonstrable UI on the standardized Paper Towel Test
  • •Willing to undergo vaginal/pelvic examination
  • •Willing and able to be compliant with visit schedule and study procedures for the study duration
  • •Provide written informed consent form
  • •Able to understand and read English

排除标准

  • •Non-ambulatory (patient confined to bed or wheelchair)
  • •Persistent pelvic pain (defined as daily pelvic pain)
  • •History of neurologic diseases (e.g. Cerebral Vasular Accident, Parkinson's disease, Multiple sclerosis, Epilepsy, Spinal cord tumor or trauma, spina bifida, current symptomatic herniated disc)
  • •Actively taking UI, OAB, or any other bladder control medication.
  • •Other urinary conditions or procedures that may affect continence status (e.g. history of bladder cancer, urethral diverticula, previous augmentation cystoplasty or artificial sphincter; implanted nerve stimulators for urinary symptoms, history of sling surgery for UI or prolapse)
  • •Participation in another research project that may influence the results of this trial
  • •Pelvic organ prolapse protruding past the introitus upon straining
  • •Absolute absence of pelvic floor muscle strength manifested by zero Brink test (Brink et al., 1994 for pressure and displacement 9
  • •Evidence of UTI or hematuria - Urine dipstick positive for red blood cells will exclude the participant from enrollment in the study until a microscopic urinalysis is negative. Urine dipstick positive for leukocytes plus nitrates will exclude the participant from enrollment in the study and require further evaluation for UTI.
  • •History of > 2 recurrent UTI's in the past year and no more than one UTI within 6 months
  • •Post void residual > 150 cc

研究组 & 干预措施

Instructional DVD Intervention

Other

Participants randomized to this arm watched an eighteen minute bladder health instructional DVD at the conclusion of a successful baseline screening visit. This intervention occurred only once

干预措施: Instructional DVD (Behavioral)

Bladder Health Class Intervention

Other

Participants randomized to this arm attended a two-hour bladder health instruction session that reviewed 3 primary self-care techniques that have been proven to prevent or lessen the severity of urinary incontinence. This session occurred only once 1-3 weeks subsequent to a successful baseline screening visit.

干预措施: Bladder Health Class (Behavioral)

结局指标

主要结局

Translating Unique Learning for Incontinence Prevention (TULIP)

时间窗: 5 years

Prevention study for Urinary Incontinence in women over the age of 55 who are fully continent (do not leak urine at all) or mildly continent (leak small drops of urine on occasion). This study will measure the effectiveness of 2 interventions: a bladder health instruction session or Bladder Health DVD administration.

次要结局

未报告次要终点

研究者

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

Carolyn Sampselle

Carolyne K Davis Professor of Nursing

University of Michigan

研究点 (2)

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