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Clinical Trials/NCT00867802
NCT00867802
Completed
Not Applicable

Mindfulness Intervention For Child Abuse Survivors

University of Maryland, Baltimore1 site in 1 country20 target enrollmentMay 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Child Abuse Survivors
Sponsor
University of Maryland, Baltimore
Enrollment
20
Locations
1
Primary Endpoint
To administer the Brief Symptom Inventory (BSI) questionnaire at each visit in order to assess psychological distress.
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

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.

Detailed Description

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

Registry
clinicaltrials.gov
Start Date
May 2007
End Date
March 2009
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Brian Berman

Director of Research Center for Integrative Medicine, University of Maryland

University of Maryland, Baltimore

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

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

Time Frame: 6 weeks

Secondary Outcomes

  • 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)

Study Sites (1)

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