18 and older, any sex, with Alcohol Use, Unspecified. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Feasibility of the Intervention - ScreeningPrimary· Day 1 of Intervention
Percent of participants who complete intervention phone call
Group
Value
95% CI
Episodic Future Thinking (EFT)
17
Volitional Choice (VC)
21
Episodic Future Thinking Plus Volitional Choice
19
Monitoring Only
18
Feasibility of the Intervention - EnrollmentPrimary· Day 1 of Intervention
Percent of participants who elect to receive text messages
Group
Value
95% CI
Episodic Future Thinking (EFT)
17
Volitional Choice (VC)
21
Episodic Future Thinking Plus Volitional Choice
19
Monitoring Only
18
Intervention Acceptability: Number of Participants Who Rated the Intervention as AcceptablePrimary· 2 Weeks Post-Intervention
Number of participants with positive acceptability ratings who indicated enjoying the intervention at least a little bit. In a phone survey, participants were asked to rate their enjoyment of the intervention on a scale of 1-5, where 1 was "not at all" and 5 was "extremely". Scores of 2 ("a little bit") or more were considered to be positive indicators of acceptability.
Group
Value
95% CI
Episodic Future Thinking (EFT)
17
Volitional Choice (VC)
19
Episodic Future Thinking Plus Volitional Choice
19
Monitoring Only
17
Alcohol ConsumptionSecondary· The 2 weeks (14-days) of the intervention period
Average number of standard drinks consumed during the 2-week intervention period per person. A "standard drink" was considered to be 12 oz beer, 1.5 ounce shot of liquor, or 5 oz glass of wine.
Group
Value
95% CI
Episodic Future Thinking (EFT)
22.1
± 25.5
Volitional Choice (VC)
17.9
± 14.9
Episodic Future Thinking Plus Volitional Choice
28.1
± 50.4
Monitoring Only
23.9
± 22.8
Sponsor's own description
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.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University of Michigan
Last refreshed: 26 March 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05235971.