Group Intervention for Interpersonal Trauma
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|ClinicalTrials.gov Identifier: NCT00348036|
Recruitment Status : Completed
First Posted : July 4, 2006
Last Update Posted : April 30, 2013
|Condition or disease||Intervention/treatment|
|Post-Traumatic Stress Disorder Depression||Behavioral: Group Intervention for Interpersonal Trauma Other: Information only|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||27 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Trauma Interventions for Low-income Women in Primary Care|
|Study Start Date :||September 2008|
|Primary Completion Date :||August 2010|
|Study Completion Date :||August 2010|
Experimental: Group therapy
Participants will receive interpersonal group therapy.
Behavioral: Group 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.
Active Comparator: Control
Participants will receive information only on PTSD.
Other: Information only
Participants will receive information about PTSD and depression, in the form of a brochures and a DVD about trauma and its emotional consequences.
- PTSD checklist [ Time Frame: Measured at baseline, Week 12, and Month 6 ]
- Hamilton Depression Inventory [ Time Frame: Measured at baseline, Week 12, and Month 6 ]
- Inventory of Interpersonal Problems [ Time Frame: Measured at baseline, Week 12, and Month 6 ]
- Health care utilization [ Time Frame: Measured at baseline, Week 12, and Month 6 ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00348036
|United States, District of Columbia|
|Washington, District of Columbia, United States, 20057|
|Principal Investigator:||Bonnie L. Green, PhD||Georgetown University Medical School Psychiatry|