N/A
Completed N=279
Dismantling the Components and Dosing of CBT for Co-Occurring Disorders
CBT Decoupling · CBT Anxiety Reduction · CBT Combined
Source: ClinicalTrials.gov NCT02161211 ↗
Enrolled (actual)
279
Serious AEs
0.0%
Results posted
Feb 2023
Primary outcomePrimary: Number of Participants That Relapsed to Drinking at 4 Months — 30; 43; 35 Participants — p=.673
Summary
The purpose of this study is to establish a brief CBT intervention that can largely, if not fully eliminate the deleterious effect of common co-occurring anxiety disorders on alcohol use disorder treatment outcomes.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants That Relapsed to Drinking at 4 Months |
30; 43; 35 | .673 |
| PRIMARY Number of Drinking Days in 4 Months Post Treatment |
8.44; 13.04; 11.34 | .133 |
| PRIMARY Number of Standard Drinks Per Drinking Day |
17.17; 17.72; 17.67 | .982 |
| SECONDARY Number of Participants Who Met SCID-IV Criteria for Alcohol Dependence at 4 Months |
13; 21; 16 | .685 |
| SECONDARY Number of Participants Who Relapsed to Hazardous Drinking |
27; 39; 34 | .608 |
Eligibility Criteria
Inclusion Criteria
- diagnostic and Statistical Manual IV diagnosis of panic disorder, generalized anxiety disorder, and/or social anxiety disorder within the past 30 days;
- inpatient treatment at Lodging Plus primarily for alcohol (vs. other drug) dependence
- alcohol use in the 30 days preceding the study
- ability to provide informed consent
- minimum of a sixth grade reading level (deemed necessary to complete study materials);
- willingness to provide contact information to confirm study follow-up appointments
- lives within proximity to the Twin Cities (e.g., within about an hour's drive) for the purpose attending follow-up visits
Exclusion Criteria
- lifetime history of psychosis or mania by history
- cognitive or physical impairment that precludes study participation
- currently and seriously suicidal (i.e., plan and intent)
Data sourced from ClinicalTrials.gov (NCT02161211). 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. Informational only — not medical advice.