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Understanding Pathways to Wellness and Recovery in Detroit - Digital Recovery Support Services

NCT07724275 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 65

Last updated 2026-07-24

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if digital recovery support services (such as smartphone app) help to support alcohol recovery. We focus on a community of Black and African American people with alcohol use disorder (AUD) who receive in-person recovery support services from a recovery community center.

Participants will:

* Have an initial 2-hour in-person visit with the research team. During this visit, participants will be asked about themselves and their recovery from alcohol problems. They will also learn about digital recovery resources.
* Use digital recovery resources on their own for 12 weeks.
* Complete a short, weekly survey about their experience using digital recovery resources.
* Have a follow-up 1-hour in-person visit where the researcher asks about again about the participants, their recovery and how they felt about using the digital recovery support services.

Conditions

Interventions

BEHAVIORAL

Digital recovery support services

The primary intervention is the provision of a menu of digital recovery support services (D-RSS) to participants, along with a phone and data plan (if needed) and technical assistance. We have created a menu of D-RSS options that have been vetted by our team as appropriate for a range of recovery goals (e.g., manage emotions, track sobriety, connect with others) and for a range of technological literacy, as well as being culturally relevant or at minimum culturally agnostic. Types of D-RSS presented to participants include mobile applications, websites, and video playlists, all of which relate to and support addiction recovery. Participants also may use other D-RSS that they identify.

Sponsors & Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

    collaborator NIH

  • Detroit Recovery Project INC

    collaborator UNKNOWN

  • Brandeis University

    lead OTHER

Principal Investigators

  • Sharon Reif, PhD · Brandeis University

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-13
Primary Completion
2026-12-31
Completion
2027-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07724275 on ClinicalTrials.gov