Pilot Testing a Novel Remotely Delivered Intensive Outpatient Program for Individuals With OUD
Recruiting
N/A
Interventional Study
Opioid Use Disorder
Serious Bacterial Infections
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 20 (estimated)
- Sponsor
- Brigham and Women's Hospital · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
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 …
Contacts