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Group Intervention for Interpersonal Trauma

Trauma Interventions for Low-income Women in Primary Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00348036
Enrollment
27
Registered
2006-07-04
Start date
2008-09-30
Completion date
2010-08-31
Last updated
2013-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Traumatic Stress Disorder, Depression

Keywords

Major Depression, Trauma, Primary Care, Low-Income Patients

Brief summary

This study will assess the acceptability and effectiveness of a six-session, modular, repeating group for low-income women who have symptoms of depression and/or post-traumatic stress disorder following interpersonal trauma exposure.

Detailed description

The aim of this study is to assess the acceptability and effectiveness of a six-session, modular, repeating group for low-income women who have symptoms of depression and/or post-traumatic stress disorder (PTSD) following interpersonal trauma exposure. Group participants will be recruited from public sector/safety net primary care clinics. Study participants will be randomized to immediate or delayed treatment. Participants in both conditions will receive information about PTSD and depression, in the form of a brochures and a DVD about trauma and its emotional consequences. Groups will be comprised of three components at each meeting: psycho-education, current relationship issues, and coping skills. Each group session will focus on a different aspect of education. Next, relationship difficulties typically associated with the symptoms discussed in that module will be addressed, and there will be group discussion about participants' relationship difficulties. Each group will end with the therapist teaching a coping skill that fits with the issues discussed earlier. Participants will be free to attend any of the sessions they missed during the first group when the group repeats. Participants in the delayed condition will be able to attend the groups after a 12-week waiting period. Assessments of PTSD, depression, functioning, and quality of life will be conducted at three time points: baseline (prior to the start of the group), 12 weeks after the start of the group, and 6 months from the start of the group. Gift cards will be sent to the women for completing each of the assessments.

Interventions

BEHAVIORALGroup Intervention for Interpersonal Trauma

Participants will receive information about PTSD and depression, in the form of a brochures and a DVD about trauma and its emotional consequences. Groups will be comprised of three components at each meeting: psycho-education, current relationship issues, and coping skills. Each group session will focus on a different aspect of education. Next, relationship difficulties typically associated with the symptoms discussed in that module will be addressed, and there will be group discussion about participants' relationship difficulties. Each group will end with the therapist teaching a coping skill that fits with the issues discussed earlier.

Participants will receive information about PTSD and depression, in the form of a brochures and a DVD about trauma and its emotional consequences.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Georgetown University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Exposure to an interpersonal traumatic event * Diagnosis of depression or PTSD (threshold or subthreshold) * Functional literacy

Exclusion criteria

* Apparent incoherence or disorientation * Apparent intoxication at recruitment * Hearing impairment

Design outcomes

Primary

MeasureTime frame
PTSD checklistMeasured at baseline, Week 12, and Month 6
Hamilton Depression InventoryMeasured at baseline, Week 12, and Month 6

Secondary

MeasureTime frame
Inventory of Interpersonal ProblemsMeasured at baseline, Week 12, and Month 6
Health care utilizationMeasured at baseline, Week 12, and Month 6

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026