Mindfulness Intervention For Child Abuse Survivors (MICAS)
NCT ID: NCT00867802
Last Updated: 2022-03-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2007-05-31
2009-03-31
Brief Summary
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Detailed Description
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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
Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Mindfulness- Based Stress Reduction: Active Comparator
Mindfulness-Based Stress Reduction program
Mindfulness-Based Stress Reduction program
Mindfulness- Based Stress Reduction comprising of 8 classes and a one-day retreat, taught over a period of 6 weeks. Intervention also includes practice at home for 20-30 minutes.
Interventions
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Mindfulness-Based Stress Reduction program
Mindfulness- Based Stress Reduction comprising of 8 classes and a one-day retreat, taught over a period of 6 weeks. Intervention also includes practice at home for 20-30 minutes.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
21 Years
65 Years
ALL
No
Sponsors
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University of Maryland, Baltimore
OTHER
Responsible Party
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Brian Berman
Director of Research Center for Integrative Medicine, University of Maryland
Principal Investigators
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Elizabeth Pradhan, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Maryland, Baltimore
Locations
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Kernan Hospital
Baltimore, Maryland, United States
Countries
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Other Identifiers
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HP-00041191
Identifier Type: -
Identifier Source: org_study_id
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