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Completed

NCT Number: NCT00867802

Mindfulness Intervention For Child Abuse Survivors (MICAS)

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.

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Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kernan Hospital

Baltimore, Maryland, 21207, United States

About this study

The specific aims of the project are:

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

mindfulness-based stress reduction program

Behavioral

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.

Primary outcomes

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

    Time frame: 6 weeks

Secondary outcomes

  1. 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)

    Time frame: 24 weeks

Sponsors and collaborators

Lead sponsor

University of Maryland, Baltimore

Other

Registry information

Official study title

Mindfulness Intervention For Child Abuse Survivors

Acronym: MICAS

Important dates

Study start
2007
Primary completion
2008
Study completion
2009
First posted
Mar 24, 2009
Registry last updated
Mar 14, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.