Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to implement a unique evidence-based intervention program to help military families deal with the critical issue of combat injury and its impact on current and future family health and functioning. The study is a randomized study. The study will compare the effects of the newly designed FOCUS-CI (Families OverComing Under Stress - Combat Injury) with the existing standard of care (SoC) at three military medical rehabilitation sites (Walter Reed Amry Medical Center, Brooke Army Medical Center and Madigan Army Medical Center) on key aspects of family health and functioning.


Clinical Trial Description

Injured service members who have at least one child between the ages of 5 and 18 years who have sustained a combat injury severe enough to require at least two weeks of inpatient hospitalization and who are within 6 months of discharge from inpatient hospitalization and currently receiving outpatient care will be recruited into this study. ;


Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01062022
Study type Interventional
Source Henry M. Jackson Foundation for the Advancement of Military Medicine
Contact
Status Terminated
Phase N/A
Start date January 2011
Completion date November 2014

See also
  Status Clinical Trial Phase
Completed NCT00990106 - Augmentation Trial of Prazosin for Post-Traumatic Stress Disorder (PTSD) N/A
Completed NCT00870545 - Reintegration: The Role of Spouse Telephone BATTLEMIND Pilot Study N/A
Completed NCT00419029 - Motivational Interviewing to Engage Operations Enduring Freedom and Iraqi Freedom (OEF/OIF) Veterans in Mental Health Treatment N/A
Terminated NCT03736356 - Long-term Health Outcomes of AE Casualties
Completed NCT00371176 - A Placebo-Controlled Trial of D-Cycloserine and Exposure Therapy for Combat-PTSD N/A
Completed NCT02809326 - Trauma Management Therapy for OEF and OIF Combat Veterans Phase 2
Active, not recruiting NCT01216982 - Effects of Omega-3 EPA/DHA for Soldiers at Risk for Mood Disorders Phase 2
Completed NCT01049516 - Prolonged Exposure for Post Traumatic Stress Disorder (PTSD) Among Operation Iraqi Freedom/Operation Enduring Freedom (OIF/OEF) Personnel N/A
Completed NCT03934658 - Remote Study of NightWare for PTSD With Nightmares N/A
Completed NCT02556645 - A Comparison of Web-Prolonged Exposure (Web-PE) and Present-Centered Therapy (PCT) for PTSD Among Active-Duty Military Personnel N/A
Completed NCT00539279 - Treatment of Older Veterans With Chronic Posttraumatic Stress Disorder N/A
Completed NCT00974402 - Psychotherapy Treatment of Deployment-Related PTSD in Primary Care Settings N/A
Enrolling by invitation NCT04040387 - Traumatic Nightmares Treated by NightWare (To Arouse Not Awaken) N/A
Active, not recruiting NCT02825602 - Vietnam Era Health Retrospective Observational Study
Completed NCT02266329 - Chronic Postconcussive Headache: A Placebo-Controlled Treatment Trial of Prazosin Phase 1/Phase 2
Completed NCT02226367 - Prazosin Augmentation of Outpatient Treatment of Alcohol Use Disorders in Active Duty Soldiers With and Without PTSD N/A
Completed NCT00475241 - Exposure Therapy for Chronic PTSD: Efficacy and Mechanisms Phase 2/Phase 3
Completed NCT00292370 - Quetiapine Augmentation for Treatment-resistant PTSD Phase 4
Completed NCT03795987 - Traumatic Nightmares Treated by NightWare (To Arouse Not Awaken) N/A
Completed NCT03337750 - An Open-Trial of Web-Prolonged Exposure (Web-PE) Among Active-Duty Military N/A