Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05054738

Impact of Combined Recovery Program and Home Telehealth Among Veterans With Substance Use Disorders in the VA Inpatient Setting

Led by VA Office of Research and Development · Updated on 2026-05-04

195

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate how well three types of treatments work to improve outcomes for Veterans with substance use problems admitted to a psychiatric inpatient unit. The study focuses on Veterans diagnosed with substance use disorders who often face challenges such as co-occurring mental illness, homelessness, and high rates of hospital readmissions. It seeks to understand if combining different treatment approaches can help reduce substance use, improve recovery, and enhance quality of life. The study compares three treatment approaches: the Combined Recovery Program (CRP), a six-session group therapy focusing on motivation and life skills provided during inpatient stay; the Stable & Able (S&A) Home Telehealth program, which offers daily support for up to three months after discharge; and Treatment-as-Usual (TAU), which includes standard inpatient mental health sessions. Participants are randomly assigned to receive CRP with TAU, CRP plus S&A with TAU, or TAU alone. The CRP and S&A aim to support recovery and stable living, including skills like money management and home maintenance. Participants start the study during their inpatient stay with CRP and/or TAU, and may continue with the S&A program after discharge. They will be evaluated at baseline, one month, and three months after treatment starts. Researchers will measure alcohol and drug use, attendance at treatment and support sessions, community involvement, mental health status, and quality of life. The study includes interviews with participants and staff to explore factors that affect treatment success. The total participation time spans from inpatient admission through three months post-discharge.

CONDITIONS

Brief Title

CRP and S&A for Inpatient Veterans

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meeting DSM-V criteria for current substance use disorder diagnosis of alcohol and/or illicit drug use
  • Used substances in the past 30 days before inpatient admission
  • Able to understand and communicate in English
  • Able to provide informed consent
  • Functioning intellectually to complete assessments
  • Willing to commit to six inpatient group therapy sessions, the Stable & Able telehealth program, and follow-up assessments at baseline, 1 month, and 3 months
Not Eligible

You will not qualify if you...

  • Hearing or vision impairments that interfere with study procedures
  • Inability to speak or understand English
  • Acute psychosis

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Inpatient Treatment

Duration - Duration of inpatient stay

Participants attend a six-session Combined Recovery Program (CRP) group during their inpatient stay, focusing on motivational enhancement and daily living skills.

Six group sessions during inpatient stay

Outpatient Treatment via Home Telehealth

Duration - 90 days after hospital discharge

Participants in the Stable & Able (S&A) program receive daily telehealth support to maintain sobriety and skills after discharge.

Daily remote contacts for up to 3 months

Follow-up Assessments

Duration - 3 months post-discharge

Participants complete follow-up assessments at 1 month and 3 months after discharge to evaluate treatment engagement, substance use, and quality of life.

2 follow-up visits (1 month and 3 months)

Trial Site Locations

Total: 1 location

1

Ralph H. Johnson VA Medical Center, Charleston, SC

Charleston, South Carolina, United States, 29401-5703

Actively Recruiting

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Research Team

E

Elizabeth J Santa Ana, PhD MA BA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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