- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00601939
Effectiveness of Empowerment Group Sessions for Treating Suicidal African American Women in Abusive Relationships
Group Interventions for Abused, Suicidal Black Women
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Most suicide attempts are a sign of great distress, often originating from depression; physical and sexual abuse; substance abuse; or family history of suicide, violence, or mental disorder. Risk factors for suicidal behavior are diverse, differing with gender, age, and ethnicity. Since the mid-1980s, the number of reported suicides and suicidal thoughts among young black individuals has increased alarmingly. The higher rates may be caused by high stress living situations attributed to poverty, abuse, discrimination, racism, and difficult family life. Therefore, cultural environments, social situations, and intrapersonal influences are important considerations in developing an effective therapy to prevent suicide. This study will evaluate the effect of culturally competent psychoeducational empowerment sessions in treating suicidal African-American women who are in abusive relationships.
The participants in this single-blind study will be randomly placed in one of two treatment groups. One group will receive psychoeducational intervention (PEI) and the other will receive enhanced treatment as usual (ETAU). After screening, eligible participants will complete a 2-hour survey about life events, concerns, and feelings with a research team member. One week later, participants will complete a second 1-hour survey. Participants will then be randomly placed in the treatment groups. Participants in both groups will receive treatment at Grady Health System, but those in the PEI group will also attend 10 weekly, 90-minute group sessions. The PEI empowerment group sessions will incorporate cultural, social, and intrapersonal elements. The ETAU group will be given mental health treatment as usual plus an adherence enhancement protocol. Follow-up surveys will occur at Week 10 (after treatment completion) and at Months 6 and 12 post-treatment.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Nadine J. Kaslow, PhD
- Phone Number: 404-616-4757
- Email: nkaslow@emory.edu
Study Contact Backup
- Name: Barbara D'Orio, MD
- Phone Number: 404-616-4760
- Email: bdorio@emory.edu
Study Locations
-
-
Georgia
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Atlanta, Georgia, United States, 30303
- Recruiting
- Grady Hospital
-
Principal Investigator:
- Nadine J. Kaslow, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Identifies as an African-American female
- Abusive relationship within the 12 months prior to study entry
- Suicide attempt within the 12 months prior to study entry
- Seeks services at Grady Health System
Exclusion Criteria:
- Score of less than 22 on Mini Mental Status Exam (MMSE)
- Score of less than 18 on Rapid Estimate of Adult Literacy in Medicine (REALM)
- Acutely psychotic
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Psychoeducational intervention (PEI)
Culturally competent group empowerment psychoeducational treatment (group intervention that is culturally informed and educational in nature)
|
PEI consists of 10 culturally competent group empowerment psychoeducational sessions.
The sessions are directed by a treatment manual and are co-led by two therapists.
The sessions are guided by the theory of triadic influence (TTI) model, which incorporates cultural-environmental influences, social-situational influences, and intrapersonal influences into treatment.
Other Names:
|
|
Active Comparator: Enhanced Treatment as Usual
Enhanced treatment as usual that includes an adherence protocol (regular care at the hospital plus an adherence protocol)
|
ETAU contains an adherence protocol plus access to weekly support group and a resource room.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Beck Scale for Suicide Ideation Score
Time Frame: Baseline, Week 10, Post-treatment Months 6 and 12
|
The Beck Scale for Suicide (BSS) Ideation consists of 19 items with responses rated on a scale from 0 to 2. Total scores range from 0 to 38 with higher scores indicating greater feelings of suicide ideation.
|
Baseline, Week 10, Post-treatment Months 6 and 12
|
|
Change in Suicide Attempt Index
Time Frame: Baseline, Week 10, Post-treatment Months 6 and 12
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Created for this study, this qualitative screening measure asks if participants have engaged in the suicidal behaviors of intentionally overdosing, cutting self, tried to shoot self or jump from a high place, tried to take life, and attempting suicide.
|
Baseline, Week 10, Post-treatment Months 6 and 12
|
|
Change in Index of Spouse Abuse Score
Time Frame: Baseline, Week 10, Post-treatment Months 6 and 12
|
The Index of Spouse Abuse (ISA) is a 30-item instrument where participants report how frequently abuse situations occur where 1 = never and 5 = very frequently.
Total scores range from 30 to 150 and higher scores indicate a higher degree of abuse.
|
Baseline, Week 10, Post-treatment Months 6 and 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Beck Depression Inventory- II
Time Frame: Baseline, Week 10, Post-treatment Months 6 and 12
|
The Beck Depression Inventory-II is a 21-item questionnaire where items are scored from 0 to 3, with higher scores assigned to more severe symptoms.
Total scores range from 0 to 63, with higher scores indicating greater severity of depressive symptoms.
|
Baseline, Week 10, Post-treatment Months 6 and 12
|
|
Change in Beck Hopelessness Scale
Time Frame: Baseline, Week 10, Post-treatment Months 6 and 12
|
The Beck Hopelessness Scale is a 20-item instrument where each statement is answered as being true or false.
Optimistic responses are scored as 0 while pessimistic responses are scored as 1.
Total scores range from 0 to 20 and higher scores indicate greater feelings of hopelessness.
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Baseline, Week 10, Post-treatment Months 6 and 12
|
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Change in Self-Efficacy Scale for Battered Women
Time Frame: Baseline, Week 10, Post-treatment Months 6 and 12
|
The Self-Efficacy Scale for Battered Women is a 12-item instrument where participants report how confident they are about performing tasks related to asking for help and taking control of their lives.
Items are scored on a scale of 0 to 100 where 0 = couldn't do it at all and 100 = completely sure I could do it.
Total raw scores range from 1 to 1200, where higher scores indicate increased self efficacy.
|
Baseline, Week 10, Post-treatment Months 6 and 12
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Nadine J. Kaslow, PhD, Emory University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00045774
- R01MH078002 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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