ovel treatments for alcohol dependence: A randomized controlled trial of structured stepped-care intervention for psychiatric comorbidity

Recruiting

• Conditions: Alcohol Dependence; Mental Health - Anxiety; Mental Health - Addiction

• Registration Number: ACTRN12607000039482
• Lead Sponsor: niversity of Sydney

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2007-01-12
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Inclusion criteria for step 1: (i) alcohol dependence according to DSM-IV criteria (Diagnostic and Statistical Manual of Mental Disorders 4th edition), with alcohol as the subject’s drug of choice, (ii) adequate cognition and English language skills to give valid consent and complete research interviews (as assessed by the mini mental state examination), (iii) willingness to give written consent, (iv) abstinence from alcohol for between 3 and 21 days (standard clinical criteria for use of acamprosate or naltrexone), (v) resolution of any clinically evident alcohol withdrawal (score 0-1 on RPA hospital alcohol withdrawal scale), and a positive score on the initial comorbidity suspicion checklist (CSC).
Entry criteria to step 2: (i) Completion of 3 weeks on acamprosate and/or natlrexone, (ii) resolution of any clinically evident alcohol withdrawal (score 0-1 on RPA hospital alcohol withdrawal scale), (iii) case formulation and diagnosis for anxiety or depression (see below).

Exclusion Criteria

Exclusion criteria for step 1: (i) sensitivity to study medications or therapy with these drugs within 6 months, (ii) active major psychiatric disorder associated with significant suicide risk, (iii) pregnancy or lactation, (iv) advanced liver disease (hepatocellular failure, variceal bleeding, ascites or encephalopathy), (v) other serious medical illness that would interfere with adherence to the study protocol.
Exclusion criteria 2: (i) Non-compliance on acamprosate and/or naltrexone, (ii) alcohol consumption at baseline levels, (iii) resolution of clinically evident anxiety or depression as assessed by the case formulation (see below). These patients will be offered further treatment as appropriate within the service and continue to be monitored.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
(i) time to relapse (>5 drinks on any one day)[Measured at week 12 (post-treatment) and week 26 (follow-up)];(ii) clinician rated severity from Anxiety Disorders Interview Schedule for DSM-IV (ADIS-IV) and Hamilton DepressionRating Scale (HDRS) on anxiety and depressive diagnoses.[Measured at week 12 (post-treatment) and week 26 (follow-up)]

Secondary Outcome Measures

Name	Time	Method
(i) time to consumption of any alcohol (lapse) identified by self-reported alcohol consumption.[Measured at week 12 (post-treatment) and week 26 (follow-up).];(ii) self-reported amount of alcohol consumed, expressed as the average consumption per drinking day.[Measured at week 12 (post-treatment) and week 26 (follow-up).];(iii) improvement in depressive or anxiety symptoms (Depression Anxiety and Stress Scale; DASS-21).[Measured at week 12 (post-treatment) and week 26 (follow-up).];(iv) biological markers of alcohol consumption at 6, 12 and 26 weeks (carbohydrate-deficient transferrin (CDT), Liver Function Tests (LFTs) and Mean Cell Volume (MCV)).[Measured at week 12 (post-treatment) and week 26 (follow-up).];(v) episodes of alcohol related harm (psychosocial, occupational, forensic, medical).[Measured at week 12 (post-treatment) and week 26 (follow-up).]