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临床试验/NCT02286115
NCT02286115已完成不适用

Life-Stress Interview for Women With Chronic Urogenital Pain Conditions

William Beaumont Hospitals2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
2
主要终点
Symptom Interpretation Questionnaire (SIQ)

研究概览

简要总结

The goal of this study is to test the efficacy, feasibility, and acceptability of providing an experiential assessment interview that targets health, and emotional and stressful experiences in a tertiary care setting specializing in women's urology.

详细描述

In this randomized, controlled trial, the investigators will compare an interview condition to a wait-list control condition. The investigators hypothesize that helping individuals identify the links between their stress, emotions, and physical symptoms will likely increase their awareness and endorsement of the link between stress and physical symptoms, including a willingness to engage in stress management techniques. It is also expected that helping raise an individual's awareness about their symptoms, followed by an experience and expression of unexpressed emotion is likely to influence their physical and psychological well-being.

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
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Participants must have a chronic urogenital pain condition

排除标准

  • non-English speaking
  • unable to read
  • psychosis
  • mental impairment

结局指标

主要结局

Symptom Interpretation Questionnaire (SIQ)

时间窗: Change from baseline symptom attribution at 6-weeks

Brief Pain Inventory (BPI)

时间窗: Change from baseline pain at 6-weeks

次要结局

  • Patient Health Questionnaire-15 (PHQ-15)(Change from baseline in symptom severity at 6 weeks)
  • Brief Symptom Inventory (BSI)(Change from baseline symptoms at 6-weeks)
  • Satisfaction With Life Scale (SWLS)(Change from baseline life satisfaction at 6-weeks)
  • Pelvic Floor Distress Inventory -20 (PFDI-20)(Change from baseline pelvic symptoms at 6-weeks)
  • Global Assessment Response (GRA)(Change from baseline overall symptoms at 6-weeks)
  • Short-Form McGill Pain Questionnaire-2 (SF-MPQ-2)(Change from baseline pain at 6-weeks)
  • Emotional Approach Coping (EAC)(Change from baseline emotional approach coping at 6-weeks)
  • Emotional Processing Scale-25 (EPS-25)(Change from baseline emotional processing at 6-weeks)
  • Inventory of Interpersonal Problems-32 (IIP-32)(Change from baseline interpersonal problems at 6-weeks)
  • Pain Catastrophizing Scale(Change from baseline pain catastrophizing at 6-weeks)
  • Change Assessment Questionnaire(Change from baseline stage of change at 6-weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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