Status:
COMPLETED
Adjunctive Family CBT for Veterans With Anxiety
Lead Sponsor:
VA Office of Research and Development
Conditions:
Anxiety Disorder
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Despite the prevalence of posttraumatic stress disorder and anxiety disorders among Veterans, there has been limited focus on the development of interventions that include family members in treatments...
Detailed Description
Posttraumatic stress disorder (PTSD) and anxiety disorders such as panic, generalized and social anxiety are highly prevalent among Veterans of all eras and negatively impact functioning and quality o...
Eligibility Criteria
Inclusion
- Veteran at least 18 years old;
- current diagnosis of at least one anxiety-based disorder: PTSD, PD, SAD, or GAD (based on ADIS-5);
- moderate-to-poor life enjoyment and satisfaction as indicated by a score of 47 or lower on the Q-LES-Q-SF
- BAI score of 16 (moderate anxiety) or higher;
- stable on psychotropic medication for 4 weeks before study participation; and
- has a family member willing to participate in the study
Exclusion
- Active symptoms of mania or psychosis at baseline (based on ADIS-5);
- depression with active suicidal ideation/intent that would preclude treatment (based on ADIS-5 \& BAI);
- moderate-to-severe cognitive impairment as indicated by a score below 20 on the SLUMS;
- active drug/alcohol abuse during the initial 3-months of study enrollment (otherwise Veterans with comorbid substance/alcohol dependence are study eligible); and
- undergoing concurrent transdiagnostic CBT for anxiety.
Key Trial Info
Start Date :
September 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 30 2024
Estimated Enrollment :
48 Patients enrolled
Trial Details
Trial ID
NCT05340478
Start Date
September 1 2022
End Date
April 30 2024
Last Update
September 5 2025
Active Locations (1)
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1
Michael E. DeBakey VA Medical Center, Houston, TX
Houston, Texas, United States, 77030-4211