Pilot Testing a Novel Remotely Delivered Intensive Outpatient Program for Individuals With OUD

Mass General Brigham

Status: Enrolling

Conditions: Serious Bacterial Infections; Opioid Use Disorder

Treatments: Behavioral: Smart IOP Intervention; Behavioral: Peer Recovery Coach

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT05817825

R21DA056799 (U.S. NIH Grant/Contract)

2023P000709

Details and patient eligibility

About

This study aims to test a remotely delivered IOP program ("SmartIOP") for OUD patients who are hospitalized for serious injection-related infections. This will be a pilot trial to assess the feasibility of the IOP program and examine OUD-related outcomes following discharge from the hospital.

Full description

The aim is to conduct a single-arm pilot study of 20 participants who are hospitalized for serious injection-related infections to complete the newly tailored program. The intervention to be developed and tested has two components: 1) the remotely delivered IOP ("Smart IOP"), and 2) a peer recovery coach who will provide support and accountability to the participant. The feasibility of the intervention will be established by evaluating recruitment and the acceptability of the program according to a priori benchmarks. The study team will assess the program's preliminary efficacy by evaluating OUD-related outcomes for up to 28 days after discharge from the hospital. The study will be conducted at Brigham and Women's Hospital (BWH), an urban, 793-bed academic medical center located in Boston, MA, and a major teaching hospital for Harvard Medical School.

Enrollment: 20 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• English-speaking adults aged 18 and above
• Any DSM-5 substance use disorder
• Can identify at least 2 individuals who can act as points of contact following discharge from the hospital

Exclusion criteria

• Psychotic disorder, active suicidality, or homicidally
• Condition likely to be terminal during the study period
• Unable to perform consent due to impaired mental status

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Treatment Group

Experimental group

Description:

The intervention to be developed and tested has two components: 1) the remotely delivered IOP ("Smart IOP"), and 2) a peer recovery coach to provide support and accountability to the participant.

Treatment:

Behavioral: Peer Recovery Coach

Behavioral: Smart IOP Intervention