N/A
N=75
Behavioral Economic Treatment to Enhance Rural (BETTER) Living
Alcohol Use, Unspecified
Bottom Line
View on ClinicalTrials.gov: NCT05235971 ↗Enrolled (actual)
75
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Feasibility of the Intervention - Screening — 17; 21; 19; 18 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Episodic Future thinking (Behavioral); Volitional choice (Behavioral); Monitoring only (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Michigan
- Primary completion
- May 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Feasibility of the Intervention - Screening |
17; 21; 19; 18 | — |
| PRIMARY Feasibility of the Intervention - Enrollment |
17; 21; 19; 18 | — |
| PRIMARY Intervention Acceptability: Number of Participants Who Rated the Intervention as Acceptable |
17; 19; 19; 17 | — |
| SECONDARY Alcohol Consumption |
22.1; 17.9; 28.1; 23.9 | — |
Summary
The purpose of this trial is to get feedback to help develop programs delivered by phone and text messages to improve wellness and health behaviors. This study will enroll adult participants that have been seen in primary care settings and live in rurally designated areas.
Eligibility Criteria
Screening Inclusion Criteria:
- adults presenting in Michigan Medicine primary care
- home address in a rurally designated area (e.g., zip code, county),
- documented alcohol use in the Electronic Health Record (EHR) (e.g., alcohol use disorder diagnosis, alcohol misuse or heavy alcohol consumption).
Baseline inclusion criteria:
- an Alcohol Use Disorders Identification Test (AUDIT-C) score of ≥3 in females or ≥4 in males
- regular access to an internet-enabled device (e.g., smart phone, computer, tablet).
Exclusion Criteria
- Does not understand English
- currently pregnant
- unable to provide informed consent due to medical/psychiatric reasons
- currently in treatment for a substance use disorder.
Data sourced from ClinicalTrials.gov (NCT05235971). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.