Feasibility of an Interdisciplinary Intervention to Improve Care Transitions for Hospitalized Patients With Substance Use Disorders

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMichael Incze

About this trial

The purpose of this study is to evaluate the feasibility and preliminary effectiveness of a primary care-based Interdisciplinary Addiction Care Transition (IntACT) team that will meet patients with substance use disorders (SUD) during a medical hospitalization and provide intensive care management, peer support, and interim SUD and medical care after discharge while facilitating a transition to long term community-based treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18 years and older

Hospitalized at University of Utah Medical Center (UUMC) for any medical reason, and

Electronic Health Record (EHR) documented diagnosis of any SUD.

Disqualifiers

Currently incarcerated

Tobacco use as only documented substance use disorder

Trial design

Design model

Parallel

Treatments tested in this trial

  • IntACT

    Behavioral

    Participants randomized to IntACT will receive usual inpatient and outpatient services plus an interdisciplinary addiction care transition team providing: (1) in-hospital discharge planning support, (2) proactive post-discharge outreach and care coordination, (3) intensive care management and peer support, and (4) interim SUD and medical care coordination for up to 4 months post-randomization, with the goal of facilitating transition to longitudinal community-based care.

  • Usual Care

    Behavioral

    Participants randomized to Usual Care will receive standard of care services routinely available at University of Utah Health, including inpatient addiction consult services when ordered, discharge planning by hospital medical and social work teams, and referrals/follow-up options based on insurance and patient preference. Usual Care participants will not receive the structured IntACT intervention components provided in the intervention arm, including proactive post-discharge outreach by the IntACT care manager/peer support specialist, intensive care management, dedicated peer navigation, scheduled interdisciplinary team review, or interim addiction/primary care transition services delivered by the IntACT team as part of the study. If a Usual Care participant independently establishes care with SPARC clinic or other services through standard referral pathways, this will be permitted and will be captured as part of outcome assessment.

Treatment groups

75 Participants
are divided into 2 treatment groups
Group A: IntACT InterventionExperimental treatment 1 intervention
Group B: Usual CareActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Care Linkage

percentage of patients who attend any follow up visit within 14 days of hospital discharge. Assessed using administrative records and patient self-report.

Time frame
14 Days
2

Retention in Treatment

Percentage of patients who have attended a medical or substance use treatment appointment within the past 30 days. Assessed at 2 months, 4 months, and 6 months after randomization. Assessed using clinic/administrative records and patient-self-report.

Time frame
6 Months
3

Intervention Feasibility

Implementation-related outcomes will be collected from N=20 clinicians who are exposed to the IntACT intervention and IntACT team members, respectively. Implementation outcomes include Feasibility, assessed via the 4-item Feasibility of Intervention measure (range 0-12, higher is more feasible)

Time frame
Completed once within 2 weeks of exposure to the intervention
4

Intervention Acceptability

Implementation-related outcomes will be collected from N=20 clinicians who are exposed to the IntACT intervention and IntACT team members, respectively. Implementation outcomes include Acceptability, assessed via the 4-item Acceptability of Intervention measure (range 0-12, higher is more acceptible)

Time frame
Completed once within 2 weeks of exposure to the intervention

Secondary outcomes

1

Time to first follow-up visit, assessed using clinic/administrative records and participant self-report.

Time until participant presents for first follow up visit.

Time frame
6 Months
2

Emergency Department visits and hospitalizations

Number of self-reported ED visits and re-hospitalizations

Time frame
6 Months
3

Substance use

Number of self-reported substance uses using Timeline Follow Back

Time frame
6 Months
4

Participant quality of life

Quality of life outcomes measured by the 12-Item Short Form Health Survey (range 0-100, hgiher score means greater quality of life), a self-reported questionnaire assessing functional health and well-being,

Time frame
6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Michael Incze

Lead sponsor

University of Utah

Sponsor institution

National Institute on Drug Abuse (NIDA)

Collaborator