Evaluation of Global Smart Drinking Goals Initiative
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: GSDG multi-component intervention.
- Who it may be relevant to
- Registry conditions: Binge Drinking, Underage Drinking, Drinking and Driving, Alcohol-Related Harms. Basic parameters: from 12 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Measurement and Evaluation of Global Smart Drinking Goals Initiative
Overview
This study will evaluate effects of a multi-component, population-level intervention on alcohol use and related harms in six intervention cities relative to six matched comparison cities. Intervention components include screening and brief interventions by health providers, other evidence-based interventions (e.g., enforcement of drink-driving or underage drinking laws), and novel or partially tested interventions that warrant further evaluation. Key outcomes of interest include alcohol-related harms such as alcohol-related motor vehicle crashes and fatalities, heavy/binge drinking, underage drinking, and drinking and driving.
Detailed description
This study will evaluate effects of a multi-component, population-level intervention on alcohol use and related harms in six intervention cities relative to six matched comparison cities. The trial is expected to expand to nine intervention and nine comparison cities in 2018. Intervention components include screening and brief interventions by health providers, other evidence-based interventions (e.g., enforcement of drink-driving or underage drinking laws), and novel or partially tested interventions that warrant further evaluation. Key outcomes of interest include alcohol-related harms such as alcohol-related motor vehicle crashes and fatalities, heavy/binge drinking, underage drinking, and drinking and driving.
Multiple years of pre- and post-intervention survey data will be collected from cross-sectional samples of adults and youth in each city to assess intervention effects on harmful alcohol use. Multiple years of archival data will also be collected from each city to assess intervention effects on alcohol-related harms such as motor vehicle crashes and fatalities, violence and unintentional injuries. Multi-level analyses will be conducted with data for the total sample of 18 cities and for each pair of cities to determine whether the overall goal of reducing harmful alcohol use by at least 10% is achieved.
Interventions
- Behavioral GSDG multi-component intervention
Multi-component intervention, including screening and brief intervention, other evidence-based interventions, and novel or partially tested interventions that warrant further evaluation.
Primary outcome measures
- Health and social harms related to alcohol use [Time frame: 1 year]
Secondary outcome measures (10)
- Heavy/binge drinking [Time frame: 1 year]
- Underage drinking [Time frame: 1 year]
- Perceived alcohol use and alcohol-related attitudes among family and friends [Time frame: 1 year]
- Alcohol expectancies [Time frame: 1 year]
- Awareness of alcohol policies [Time frame: 1 year]
- Perceived enforcement of alcohol policies [Time frame: 1 year]
- Awareness of chronic health risks associated with alcohol use [Time frame: 1 year]
- Awareness of alcohol health guidance labels and information [Time frame: 1 year]
- Consumption of no-alcohol and low-alcohol beer [Time frame: 1 year]
- Screening and brief intervention for heavy/binge drinking [Time frame: 1 year]
Eligibility criteria
Inclusion criteria
- At least 12 years old
- Parental consent is be required if under 18 years old
Exclusion criteria
- Institutionalized individuals
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Prevention
Study locations
United States · 1 center
- HBSA — Calverton
Identifiers
NCT: NCT03262259 · 0881