N/A
N=6
Team Based Initiative Support
Traumatic Brain Injury
Bottom Line
View on ClinicalTrials.gov: NCT00771277 ↗Enrolled (actual)
6
Serious AEs
—
Results posted
Sep 2014
Primary outcome: Primary: Number of Participants Who Reported 5 Themes — 6; 6; 6; 6 participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Support Teams (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- US Department of Veterans Affairs
- Primary completion
- Mar 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Who Reported 5 Themes |
6; 6; 6; 6; 6 | — |
| SECONDARY PHQ-9 |
11.5 | — |
| SECONDARY Zarit Burden Inventory |
23.0 | — |
Summary
Traumatic brain injury (TBI) has been called the signature injury of the Iraq War. This pilot study investigated family needs of 6 rural families caring for a Veteran with TBI. Two Veterans had moderate TBI and all had comorbid post traumatic stress disorder diagnoses. The veterans were 1 to 5 years post-injury. Families were reluctant to include others in helping the family because of privacy concerns, desire for independence, and negative employment repercussions if the extent of the TBI deficit became known in the community. Most were still employed, despite TBI deficits. Despite having previously received information, families still had substantial needs for information about the condition and its prognosis and sequelae (e.g., why things happen, unsafe/frightening behaviors, work, finances, communication changes) and the availability and types of services (e.g., who to contact, benefits, help needed)
Eligibility Criteria
Inclusion Criteria
- The primary family member caregiver of the Traumatic Brain Injury (TBI) veteran
- Veteran receiving care at the Memphis Veterans Affairs Medical Center
- Perceived need of help and support
- Willing to participate in the study after discussion with OEF/OIF Program
- Manager or team member
Exclusion Criteria
- None
Data sourced from ClinicalTrials.gov (NCT00771277). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.