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临床试验/NCT00867802
NCT00867802已完成不适用

Mindfulness Intervention For Child Abuse Survivors

University of Maryland, Baltimore2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2007年5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
20
试验地点
2
主要终点
To administer the Brief Symptom Inventory (BSI) questionnaire at each visit in order to assess psychological distress.

研究概览

简要总结

The purpose of this study is to assess the effect of meditation training called Mindfulness-Based Stress Reduction on reducing the symptoms of psychological distress among adult survivors of child abuse.

详细描述

The specific aims of the project are:

  1. To determine whether Mindfulness- Based Stress Reduction program is associated with a reduction in symptoms of depression, anxiety, and psychological distress.
  2. To assess indications of efficacy, assess feasibility of enrollment and compliance among this patient population
  3. Provide pilot data that can be used to apply for larger grants to more fully develop this approach

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
21 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A history of child abuse, as attested by the potential participant
  • Currently in therapy with a licensed psychotherapist (psychiatrist, psychologist, social worker).
  • Plans to remain in therapy with a licensed psychotherapist (psychiatrist, psychologist, social worker) for the duration of the study.
  • Recommendation made by the potential participant's licensed psychotherapist (psychiatrist, psychologist, social worker) the Mindfulness-Based Stress Reduction program would be an appropriate adjunct therapy for his or her client.
  • Score of 0.50 or higher on the General Severity Index of the Brief Symptom Inventory, indicating psychological distress above the normal population.
  • Aged 21 or above.
  • Ability to read and write English.
  • Able to attend 10 courses and assessment visits over a 6-week period.
  • Willing to practice skills for 20-30 minutes per day 6 days a week, during the course.

排除标准

  • Major psychiatric illness (bipolar disorder, schizophrenia, dissociative identity disorder, or others).
  • Active alcoholism or drug dependency.
  • Any psychological or physical illness the investigator feels would prohibit full participation in the course.
  • Currently enrolled in another clinical trial.

结局指标

主要结局

To administer the Brief Symptom Inventory (BSI) questionnaire at each visit in order to assess psychological distress.

时间窗: 6 weeks

次要结局

  • Trauma Symptom Inventory to all participants at each visit. Administer the Beck Depression Inventory (BDI) to all participants. Functional Assessment of Chronic Illness Therapy spiritual Well-Being (FACIT-SP)(24 weeks)

研究者

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

Brian Berman

Director of Research Center for Integrative Medicine, University of Maryland

University of Maryland, Baltimore

研究点 (2)

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