Traumatic Brain Injuries Clinical Trial
Official title:
Cognitive Behavioral Therapy (CBT) for Caregivers of Operation Iraqi Freedom/Operation Enduring Freedom (OIF/OEF) Service Members With Combat-Related Traumatic Brain Injuries (TBI)
Verified date | February 2024 |
Source | University of Alabama at Birmingham |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary purpose of this research is to evaluate the impact of a telehealth-based, cognitive behavioral therapy (CBT) intervention (problem-solving training: PST) for adult informal military family/friend caregivers of OIF/OEF service members with a deployment-related TBI.
Status | Completed |
Enrollment | 213 |
Est. completion date | December 2016 |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: - Age = 19 years old - Meets study project definition of a military caregiver - Documentation or determination of an OIF/OEF deployment related TBI - Service member will have presented to a Veterans Administration Medical Center (VAMC) or military medical center - English-speaking - Has access to a telephone for the administration of measures and/or intervention calls - Has no significant cognitive or communication problems that might significantly interfere with adequately understanding information or talking on the telephone which will be determined by the clinical judgment of the person consenting the participant. Exclusion Criteria: - Has a life-threatening or other serious disease that impacts the ability to participate for the duration of the project - No determination or documentation of a deployment-related TBI related to OIF/OEF for the injured service member - Has a severe hearing impairment that impedes communication and standardized implementation of the intervention and telephone follow-up - Formal caregiver - Caregiver does not want to participate |
Country | Name | City | State |
---|---|---|---|
United States | University of Alabama at Birmingham | Birmingham | Alabama |
Lead Sponsor | Collaborator |
---|---|
University of Alabama at Birmingham |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Patient Health Questionnaire-9 | Change from baseline in PHQ-9 scores at post-program (3-months follow-up) |
Status | Clinical Trial | Phase | |
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