Depression Clinical Trial
Official title:
Mission Reconnect: Promoting Resilience and Reintegration of Post-Deployment Veterans and Their Families
Verified date | July 2015 |
Source | Collinge and Associates, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
An urgent and growing need exists for interventions that support the long-term adjustment and mental health needs of OIF/OEF veterans and their relationship partners after the return from deployment. This project will complete production of a multimedia intervention program for autonomous use, delivered by Internet and mobile app technology, that teaches couples selected mind/body interventions and massage techniques to promote stress reduction, compassion, resiliency and relationship re-integration. A four-armed randomized trial will evaluate mental health outcomes as a free-standing program and as complementary to a current standard of care structured group program.
Status | Completed |
Enrollment | 320 |
Est. completion date | May 2015 |
Est. primary completion date | May 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Veteran of deployment in Operation Iraqi Freedom (OIF) or Operation Enduring Freedom (OEF) - Partner or spouse of the veteran (veteran and partner/spouse must participate together in the project) Exclusion Criteria: - Couples are ineligible who have previously attended a PREP for Strong Bonds program |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Collinge and Associates, Inc. |
Collinge W, Kahn J, Soltysik R. Promoting reintegration of National Guard veterans and their partners using a self-directed program of integrative therapies: a pilot study. Mil Med. 2012 Dec;177(12):1477-85. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Perceived Stress Scale (PSS-10) | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Primary | Change in Beck Depression Inventory (BDI) | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Primary | Change in Posttraumatic Checklist-Civilian (PCL-C) | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Primary | Change in The Self-Compassion Scale | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Primary | Change in Responses to Stressful Experiences Scale (RSES) | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Secondary | Change in Multidimensional Perceived Social Support Scale (MPSSS) | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Secondary | Change in Pittsburgh Sleep Quality Index | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Secondary | Change in Revised Dyadic Adjustment Scale (RDAS) | Change from baseline to 2 months and 4 months | Baseline, 2 months, 4 months | No |
Secondary | Investigator-generated survey of use of stress reduction practices | Weekly for 8 weeks, then at 4 months | No | |
Secondary | Investigator-generated survey on use of massage and massage effects | Weekly for 8 weeks | No | |
Secondary | Investigator-generated survey on self-efficacy using massage, and satisfaction giving and receiving the use of massage | 2 months, 4 months | No | |
Secondary | Investigator-generated ratings of program satisfaction | 4 months | No |
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