Condition: Posttraumatic Stress Disorder · Alcohol Use Disorder · Sponsor: Texas A&M University
The goal of this clinical trial is to test the efficacy of a novel integrative cognitive-behavioral intervention in patients with posttraumatic stress disorder (PTSD) and alcohol use disorder (AUD). Specific Aim 1: Examine the efficacy of CPT-RP, as compared to RP alone, in reducing alcohol frequency (percent days drinking) and quantity (drinks per drinking day) as measured by the Timeline Follow-Back (TLFB). Specific Aim 2: Examine the efficacy of CPT-RP, as compared to RP alone, in reducing PTSD symptoms as measured by the Clinician Administered PTSD Scale (CAPS-5). Specific Aim 3: Use ecological momentary assessment (EMA) to evaluate intervention effects on daily alcohol-related cognitions and behaviors through real-time associations with PTSD symptomatology and distress tolerance. Researchers will compare integrative CPT+RP with RP-alone to see if CPT+RP is more efficacious in reducing alcohol use and PTSD symptom severity.
This description comes directly from the study's public registry record.
Anka A Vujanovic, Ph.D. · 979-862-6538 · avujanovic@tamu.edu
Sudie E Back, Ph.D. · backs@musc.edu
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| Medical University of South Carolina | Charleston, South Carolina, United States | Recruiting |
| Texas A&M University | College Station, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05959434