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Family Involvement in Treatment for PTSD
This study is ongoing, but not recruiting participants.

First Received on May 1, 2009.   Last Updated on October 31, 2011   History of Changes
Sponsor: Department of Veterans Affairs
Information provided by (Responsible Party): Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00893152
  Purpose

Post-traumatic stress disorder (PTSD), a potentially severe and persistent condition that affects social, occupational and family functioning, is prevalent among returning OIF/OEF veterans. PTSD has a powerful impact on family functioning. Because good family relationships appear to moderate its impact, while stressful relationships may reduce the benefits of treatment, a program that enhances family functioning by assisting both veteran and family in coping with the veteran's PTSD could directly improve the veteran's adjustment and well-being, and indirectly improve his/her social and occupational functioning. Effective programs for OIF/OEF veterans are urgently needed. This study will address critical gaps in knowledge about relevant needs and preferences of OIF/OEF veterans and families, and how best to involve families in treatment.


Condition
Posttraumatic Stress Disorder

Study Type: Observational
Official Title: Perspectives on Enhancing Family Involvement in Treatment for PTSD

Resource links provided by NLM:


Further study details as provided by Department of Veterans Affairs:

Primary Outcome Measures:
  • Qualitative Interviews - Perspectives on Family Involvement in PTSD Treatment [ Time Frame: Current ] [ Designated as safety issue: No ]

Estimated Enrollment: 160
Study Start Date: November 2009
Estimated Study Completion Date: December 2011
Primary Completion Date: September 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
Male veterans (focus groups and individual interviews)
2
Female veterans (focus groups and individual interviews)
3
Family members of participating veterans (focus groups and individual interviews)

Detailed Description:

Background: Post-traumatic stress disorder (PTSD), a potentially severe and persistent condition that affects social, occupational and family functioning, is prevalent among returning OIF/OEF veterans. PTSD has a powerful impact on family functioning. Because good family relationships appear to moderate its impact, while stressful relationships may reduce the benefits of treatment, a program that enhances family functioning by assisting both veteran and family in coping with the veteran's PTSD could directly improve the veteran's adjustment and well-being, and indirectly improve his/her social and occupational functioning. Effective programs for OIF/OEF veterans are urgently needed. This study will address critical gaps in knowledge about relevant needs and preferences of OIF/OEF veterans and families, and how best to involve families in treatment.

Objectives: The specific aim of this project is to describe the needs and preferences of OIF/OEF service-era veterans with PTSD and their families relevant to family involvement in care.

Methods: This is a two-site qualitative methods study that will be conducted at the Little Rock and Oklahoma City VAMCs. The study will involve approximately 160 participants (80 veterans and 80 family members). We will use qualitative methods to identify the needs and preferences of OIF/OEF veterans and family members, and will assess the implications of study findings for program design. We will conduct individual and group interviews in Little Rock and Oklahoma City with 40 male veterans. We will conduct separate individual and group interviews in Little Rock and Oklahoma City with 40 female veterans, and with 80 family members of participating veterans in Little Rock and Oklahoma City. Interviews will address perceived needs, desires for family involvement in treatment, types of services that would be attractive/unattractive, elements of alternative approaches to meeting needs that would be attractive/unattractive, as well as logistic considerations (e.g., timing and frequency of meetings, mode of meeting, child care). We will use the techniques of constant comparison and content analysis to analyze interview data.

Status: Data collection is complete; data analysis is ongoing.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Veteran participants will be OIF/OEF veterans receiving outpatient treatment for PTSD at the Little Rock or Oklahoma City VAMCs. Each veteran participant will designate an adult family member/friend to participate in a separate interview.

Criteria

Inclusion Criteria:

Veteran:

  1. Age 18-65;
  2. 2 or more inpatient or outpatient mental health contacts at LR or OKC VAMC in the previous 12 months with a primary diagnosis of PTSD;
  3. Served in Iraq or Afghanistan since 10/7/01;
  4. Have a family member who may be willing to participate in the focus group.

Family:

  1. Age > 18
  2. English speaking
  3. Be the designated "family member" of a participating veteran

Exclusion Criteria:

  • Non-English speaking
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00893152

Locations
United States, Arkansas
Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock
No. Little Rock, Arkansas, United States, 72114-1706
United States, Oklahoma
VA Medical Center, Oklahoma City
Oklahoma City, Oklahoma, United States, 73104
Sponsors and Collaborators
Investigators
Principal Investigator: Ellen P. Fischer, PhD Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock
  More Information

No publications provided

Responsible Party: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00893152     History of Changes
Other Study ID Numbers: DHI 08-097, CAVHS 0156_2008I
Study First Received: May 1, 2009
Last Updated: October 31, 2011
Health Authority: United States: Federal Government

Additional relevant MeSH terms:
Stress Disorders, Post-Traumatic
Stress Disorders, Traumatic
Anxiety Disorders
Mental Disorders

ClinicalTrials.gov processed this record on February 09, 2012