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临床试验/NCT00297427
NCT00297427已完成2 期

Efficacy of Acupuncture in Treating Urinary Incontinence

University of Pittsburgh2 个研究点 分布在 1 个国家目标入组 127 人开始时间: 2005年10月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
127
试验地点
2
主要终点
Percent Change in Incontinent Episodes

研究概览

简要总结

This research study will evaluate the effectiveness of acupuncture in decreasing urinary incontinence (involuntary urine loss) in women. The study will involve 12 acupuncture sessions over 6 weeks. We will compare the effectiveness of acupuncture and sham (placebo) acupuncture (a procedure in which the needle feels like it penetrates the skin, but is not actually inserted into the body) on the frequency and volume of involuntary (accidental) urine loss after completing the intervention, and again one month later. Individuals participating in this study will be randomly assigned to receive either the actual or sham acupuncture. Randomization means being assigned by chance, similar to flipping a coin. Study participants will not know which group (actual or sham acupuncture) they were assigned to until one month after completing the 6-weeks of treatment. The sham acupuncture needles look similar to the real acupuncture needles and feel like they penetrate the skin, but do not actually do so. If individuals are assigned to the sham acupuncture group, they will be eligible to receive the actual acupuncture one month after completing the sham acupuncture if they wanted to. All individuals will be followed for 6 months after completing the acupuncture treatments.

详细描述

See Brief Summary

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Urge or stress urinary incontinence at least twice a week on average for at least 3 months

排除标准

  • History of previous acupuncture
  • History of a neurologic problem such as Parkinson's disease or multiple sclerosis that could affect bladder function
  • Current treatment with overactive bladder medications or medications that relax the bladder
  • Urinary catheter
  • Pregnancy
  • Inability to empty the bladder effectively
  • Inability to toilet independently
  • Current treatment with steroid
  • Interstitial cystitis
  • Chronic pelvic pain
  • Current treatment with warfarin

结局指标

主要结局

Percent Change in Incontinent Episodes

时间窗: 4 weeks post true or sham acupuncture

Percent change in incontinent episodes (measured by self-report electronic bladder diary) 4 weeks post true or sham acupuncture

Physical Health-Related Quality of Live

时间窗: 1 Week post-intervention

Percent change in physical health related quality of life measured at 1 week post-intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Physical Component score. Higher SF-36 Physical Component scores are considered a better outcome.

Physical Health-Related Quality of Life

时间窗: 4-weeks post-intervention

Percent change in physical health related quality of life measured at 4 weeks post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Physical Component score. Positive change indicates an increase in physical health-related quality of life.

Mental Health Related Quality of Life

时间窗: 4 weeks post true or sham acupuncture

Percent change in mental health related quality of life measured at 4 weeks post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Mental Health Component score.

Incontinence-Specific Quality of Life

时间窗: 4-weeks post-intervention

Percent change in incontinence-specific quality of life a 4 weeks post-intervention (true or sham acupuncture) measured by the Incontinence Impact Questionnaire. Positive changes indicate improvement in incontinence-specific quality of life.

Duration of Any Beneficial Effects

时间窗: monthly during follow-up up to 6 months

Time to relapse in months of participants who completed true acupuncture initially or who crossed-over following sham (offered to all sham participants)

次要结局

  • Change in Bladder Capacity(Change from baseline to 4 weeks post-intervention)
  • Urodynamic Diagnostic Impression of Stress Urinary Incontinence(Baseline and 4 weeks post-treatment)
  • Urodynamic Impression of Urge Urinary Incontinence(Baseline and 4 weeks post true or sham acupuncture)
  • Characteristics of Responders Based on Glasses/Cups Per Day of Non-caffeinated Fluids (Including Water)(Baseline)
  • Characteristics of Responders: Duration of Urinary Incontinence (UI) in Years(Baseline)
  • Adherence to Treatment Protocol(6 weeks)
  • Burden Associated With the Acupuncture Treatment Protocol(1 week post-treatment)
  • Need for Booster Acupuncture During Follow-up(Monthly during the 6 month follow-up period)
  • Response to Booster Acupuncture if Needed(After the booster sessions)
  • Pelvic Floor Muscle Strength(Baseline and 4 weeks post true or sham acupuncture)

研究者

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

Sandra Engberg

Professor and Associate Dean for Graduate Clinical Education

University of Pittsburgh

研究点 (2)

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