Status:

COMPLETED

Mindfulness Intervention For Child Abuse Survivors (MICAS)

Lead Sponsor:

University of Maryland, Baltimore

Conditions:

Child Abuse Survivors

Eligibility:

All Genders

21-65 years

Phase:

NA

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 abu...

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...

Eligibility Criteria

Inclusion

  • 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

  • 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.

Key Trial Info

Start Date :

May 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 1 2009

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT00867802

Start Date

May 1 2007

End Date

March 1 2009

Last Update

March 14 2022

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Kernan Hospital

Baltimore, Maryland, United States, 21207