Project POINT: Effectiveness and Scalability of an Overdose Survivor Intervention (POINT)
Substance Use Disorders, Overdose
About this trial
This is an interventional supportive care trial for Substance Use Disorders focused on measuring Opioid Use Disorder, Peer Recovery Coach
Eligibility Criteria
Inclusion Criteria:
- Revived from a drug overdose or admitted to the ED for an opioid-related health issue, including opioid withdrawal, abscess (from IV opioid use), endocarditis (from IV opioid use), or active opioid intoxication
- Score at least "1" on the DSM-5 for Opioid Use Disorder screening tool
- Eligible for discharge from the Methodist or Ball Memorial Hospital Emergency Department and deemed able to speak to research staff by ED staff
- Be 18 or older
- Be medically stable (i.e., cleared to leave the ED by a physician) and capable of providing consent.
(Individuals discharged from the ED during a POINT shift who do not wish to participate in the study are still eligible to receive POINT services.)
Sites / Locations
- Indiana University Health Methodist Hospital
- Indiana University Health Ball Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
POINT
Standard Care
This arm will be offered both POINT services (in addition to standard emergency care) and enrollment in study data collection. If they choose to enroll in POINT, they may choose whether or not to enroll in data collection, as it is not required. Should they enroll in data collection, they will be consented and enrolled in the research study as a participant in the POINT study arm.
This arm will only be offered enrollment in study data collection, as they will receive standard emergency care. If they choose to enroll, they will be consented in the research study as the Standard Care arm.