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Clinical Trials/NCT03573167
NCT03573167
Completed
Not Applicable

Mobile Phone-Based Motivational Interviewing to Reduce Alcohol Use Problems in Kenya

University of Vermont0 sites322 target enrollmentSeptember 30, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alcohol Use Disorder
Sponsor
University of Vermont
Enrollment
322
Primary Endpoint
Reduction in alcohol use score as measured by the Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) from baseline to one (1) month.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The primary objective of this study was to test whether motivational interviewing (MI) provided over the mobile phone would reduce alcohol use among adults, including people living with HIV/AIDS, visiting primary care in Kenya. Heavy alcohol users voluntarily consented to being randomized to one of three study arms: standard in-person MI, mobile MI, or waitlist control receiving no intervention for 1 month followed by mobile MI. Alcohol use problems were assessed using validated screeners and changes in alcohol use were assessed at 1 month and 6 months after receiving the intervention. The investigators hypothesized that alcohol use would reduce after MI treatment compared to waitlist control, there would be no difference between standard in-person MI and mobile MI, and these reductions would be sustained out to six months following the intervention.

Registry
clinicaltrials.gov
Start Date
September 30, 2014
End Date
December 31, 2015
Last Updated
7 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Valerie Harder

Associate Professor

University of Vermont

Eligibility Criteria

Inclusion Criteria

  • Adults visiting the primary care clinic and screening positive for potential alcohol use problems.

Exclusion Criteria

  • Persons younger than 18 years old, with severe psychiatric morbidity, or cognitive impairment were not eligible for the study

Outcomes

Primary Outcomes

Reduction in alcohol use score as measured by the Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) from baseline to one (1) month.

Time Frame: 1 month

The investigators compared the change in AUDIT-C alcohol use score from baseline to one (1) month after the intervention between the investigators' three study arms.

Reduction in alcohol use score as measured by the Alcohol Use Disorders Identification Test (AUDIT) and AUDIT-C from baseline to six (6) months.

Time Frame: 6 months

The investigators compared the change in AUDIT and AUDIT-C alcohol use scores from baseline to six (6) months after the intervention between the investigators' two active study arms: 1) In-Person Motivational Interviewing (MI) and 2) Mobile MI.

Secondary Outcomes

  • Reduction in alcohol use score as measured by the AUDIT and AUDIT-C moderated by HIV co-morbidity from baseline to one (1) month and from baseline to six (6) months.(1 and 6 months)
  • Reduction in alcohol use score as measured by the AUDIT moderated by mental health co-morbidity, as measured by the Achenbach System of Empirically Based Assessments (ASEBA) Adults Self-Report, from baseline to six (6) months.(6 months)

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