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Clinical Trials/NCT00998959
NCT00998959
Completed
Not Applicable

Feasibility and Efficacy of a Stress Reduction Intervention for Enhancing Treatment Outcome for Depressed Minority Patients

Trina E. Chang, MD1 site in 1 country40 target enrollmentAugust 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Major Depressive Disorder
Sponsor
Trina E. Chang, MD
Enrollment
40
Locations
1
Primary Endpoint
Feasibility (rate of enrollment, attrition)
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to determine the usefulness of a stress reduction treatment in helping minority patients with major depression get better. Subjects will receive six weeks of either mindfulness-based stress reduction and problem solving therapy or psychoeducation.

Detailed Description

The purpose of this study is to determine the usefulness of a stress reduction treatment compared to psychoeducation in helping minority patients with major depression get better. The study will last 10 weeks. During the main portion of the study, subjects will receive either individual weekly sessions of stress-reduction therapy or psychoeducation for six weeks. The stress reduction therapy will consist of mindfulness-based stress reduction and problem solving therapy, which focuses on linking psychological problems with psychosocial issues and helping you use your skills and resources to improve your functioning. The psychoeducation will consist of six sessions of education on depression and the treatment and management of symptoms. Each session will last 50 minutes, and four of the visits will also include filling out questionnaires which will take approximately 15-30 minutes to complete. One month after the last session, subjects will come in for a follow-up visit with a study clinician to see how they are doing and to fill out questionnaires.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
January 2012
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Trina E. Chang, MD
Responsible Party
Sponsor Investigator
Principal Investigator

Trina E. Chang, MD

Staff Psychiatrist

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Meet criteria for current major depressive disorder
  • Men or women aged 18-75 who self-identify as a member of a racial or ethnic minority group
  • Has a PCP, therapist, psychiatrist, etc aware of their depression. Or, subject agrees to seek outside mental health treatment/management

Exclusion Criteria

  • Pregnancy

Outcomes

Primary Outcomes

Feasibility (rate of enrollment, attrition)

Time Frame: 2 years

Secondary Outcomes

  • Perceived stress(Week 10)

Study Sites (1)

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