Alcohol Drinking Clinical Trial
— CTMIOfficial title:
A Randomized Clinical Trial of Culturally Tailored Motivational Interviewing
| Verified date | March 2019 |
| Source | Northeastern University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Culturally-tailored empirically-based interventions are needed because Latinos suffer a greater burden of alcohol-related health disparities and negative social consequences compared to other racial/ethnic groups, are less likely to initiate and to remain in treatment, and are more likely to live in communities with a high density of alcohol outlets. Pilot data from the PI's (New Investigator) K award (AA014905), which will serve as the basis for the current proposed larger-scale study, demonstrated that culturally tailored motivational interviewing (CTMI) outperformed motivational interviewing (MI) that was not tailored to the needs of Latino heavy drinkers. The public health impact of this study will be to develop a program of early screening and brief intervention to reduce hazardous drinking among Latinos, to minimize the burden of illness and social consequences that disproportionately affect Latino communities.
| Status | Completed |
| Enrollment | 301 |
| Est. completion date | November 30, 2017 |
| Est. primary completion date | October 30, 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Meet criteria for hazardous drinking (greater than or equal to 5/4 per occasion for males/females), two or more times in the past 30 days. - Latino - Are not currently in any substance use treatment program for alcohol use disorder, nor have been in the past year. - 18-65 years old - Able to speak English or Spanish Exclusion Criteria: - Psychotic symptoms, as evidenced by hallucinations or delusions. - Cognitive impairment, as evidenced by inability to understand informed consent. a. To determine comprehension, a research assistant will read informed consent aloud and will ask 3 questions 1. Is the study voluntary 2. Can he/she drop out at any time 3. Will there be study follow-up. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Northeastern University | Boston | Massachusetts |
| United States | South End Community Health Center | Boston | Massachusetts |
| Lead Sponsor | Collaborator |
|---|---|
| Northeastern University |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in Frequency of Heavy Drinking Days | The frequency of heavy drinking days will be assessed using a 90 day Timeline Follow Back (TLFB) collected at baseline prior to study intervention. TLFB will be administered again at the 3-, 6-, and 12-month follow up periods. Changes in frequency of heavy drinking days will be assessed across all study time points. | Baseline, 3-, 6-, and 12-month follow-up | |
| Secondary | Change in Frequency of Alcohol-Related Negative Consequences | Frequency of alcohol-related consequences will be assessed using the Drinker Inventory of Consequences (DrInC) and its' five subscales, as well as the Drinking and Driving Scale. The DrInC will be administered at baseline, 3-, 6-, and 12-month follow up whereas the Drinking and Driving scale will be administered at baseline and again at the 12-month follow up session. Changes in the frequency of reported negative alcohol-related consequences will be examined across these time points. | Baseline, 3-, 6-. 12-month follow up |
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