Test of a new motivational intervention for alcohol misuse,incorporating mobile phone reminders
- Conditions
- Risky alcohol useMental Health - Addiction
- Registration Number
- ACTRN12614000720617
- Lead Sponsor
- Institute of Health and Biomedical Innovation, Queensland University of Technology
- Brief Summary
Samples from this trial and the trial of 12614000718640 were combined for the analysis. FIT gave substantial reductions in alcohol consumption, which were similar to or greater than within-condition effects obtained in studies with similar samples that offered extensive alcohol control skills training. At the final assessment, all but 11% had some reduction in weekly drinking below Baseline levels, although only 22% were below both weekly and single-occasion criteria for risky drinking over the previous month.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 14
Weekly alcohol intake of greater than 140g in total (14 Australian standard drinks)
Access to an iPhone or iPad
Injected drug use in the past month
Daily use of illicit substances
History of psychosis, brain injury, intellectual disorder, or dementia
Current pregnancy
High dependence on medical care
Current suicide risk
Self harm requiring treatment within the previous 12 months
Current engagement in other treatment for alcohol use
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in the number of standard drinks consumed weekly, as measured by the Timeline Follow Back[6 months following initial screening]
- Secondary Outcome Measures
Name Time Method Increase in: <br>*Salience of cues consistent with abstinence/reduced drinking (as measured by the Goal Motivation Scale).[6 months following baseline evaluation];Increase in:<br>*Elaboration of adaptive thoughts about alcohol (as measured by the Goal Motivation Scale).<br>[6 months following baseline evaluation];Increase in: <br>*Vividness of imagery (as measured by participant-reported ratings of vividness following in-session imagery practice).[6 months following baseline evaluation]