Clinical Trial: The Trauma Recovery and Resiliency Research Project
This study is currently recruiting patients.
Verified by Cambridge Health Alliance August 2005
| Sponsored by: | Cambridge Health Alliance | | Information provided by: | Cambridge Health Alliance | | ClinicalTrials.gov Identifier: | NCT00131534 | |
Purpose
The overall purpose of this study is the assessment of treatment outcome among traumatized patients seeking individual and/or group
therapy at the Victims of Violence Program. The study gathers information from patients using quantitative (self-report) and qualititative (interview-based) approaches, to determine changes in
symptom patterns and domains of functioning relevant to psychological trauma.
| Condition | Intervention | Phase |
Posttraumatic Stress Disorders
| Behavior: Individual therapy Behavior: Group therapy
| Phase II
|
MedlinePlus related topics: Post-Traumatic Stress Disorder
Study Type: Observational
Study Design: Natural History, Longitudinal, Defined Population, Prospective Study
Further Study Details:
Expected Total Enrollment: 1000
Study start: August 1991; Expected completion: August 2010
Last follow-up: August 2005; Data entry closure: April 2010
The focus of the Trauma Recovery and Resiliency Project is the evaluation of treatment outcome among complexly traumatized patients seeking individual and/or group
therapy at the Victims of Violence (VOV) Program, a specialty clinic located in the
Outpatient Psychiatry Department of the Cambridge Health Alliance and affiliated with Harvard Medical School. The project has two major components: (1) All patients seeking VOV treatment are administered a battery of self-report measures assessing symptoms associated with complex trauma (i.e., interpersonal trauma that is usually repeated and prolonged) (2) A subsample of patients are interviewed using the Multidimensional Trauma Recovery and Resiliency Interview (MTRRI) and its companion rating scale (MTRR; Harvey et al, 1994, 2000, 2003) to assess trauma impact, recovery and resiliency on eight domains of psychological functioning. Data is analyzed using quantitative and qualitative approaches to evaluate treatment effectiveness and elucidate the recovery trajectories of patients receiving VOV treatment.
Eligibility
Ages Eligible for Study: 18 Years - 65 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- In individual or group therapy at VOV program
- Consents to research participation
Exclusion Criteria:
- Insufficient proficiency in English to complete self-report measures and/or interview
- Research participation clinically counterindicated
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00131534
Michaela Mendelsohn, Ph.D. (617) 575-5283 mmendelsohn@challiance.org
Kelley Callahan, Ph.D. (617) 575-5314 kcallahan@challiance.org
Massachusetts Victims of Violence Program, Cambridge Health Alliance, Somerville, Massachusetts, 02143, United States; Recruiting
Michaela Mendelsohn, Ph.D. 617-575-5283 mmendelsohn@challiance.org
Bernadette Louis (617) 591-6361 blouis@challiance.org
Study chairs or principal investigators
Mary R. Harvey, Ph.D., Principal Investigator, Victims of Violence Program, Cambridge Health Alliance
Judith L. Herman, MD, Principal Investigator, Victims of Violence Program, Cambridge Health Alliance
More Information
Publications
Harvey MR. An ecological view of psychological trauma and trauma recovery. J Trauma Stress. 1996 Jan;9(1):3-23.
Study ID Numbers: CHA-IRB-0031/01/04
Last Updated: August 17, 2005
Record first received: August 16, 2005
ClinicalTrials.gov Identifier: NCT00131534
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-08-23
Source: ClinicalTrials.gov
Cache Date: August 24, 2005