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Enrolling By Invitation NCT07886944

PATH to Reducing Burnout Among Peers Who Deliver Overdose Prevention Services (R33 Phase Clinical Trial)

Conditions: Burnout, Secondary Trauma, Compassion Fatigue, Opioid Use Disorder, Stimulant Use Disorder, Substance Use Disorder

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 200
Sponsor: Chestnut Health Systems

Location: Chestnut Health Systems Lighthouse Institute Chicago Illinois

Summary

The investigators propose to test the effectiveness of PATH (Peer Advanced Training for total Health) as an educational workforce intervention for improving peer recovery support specialists' (PRSS) overdose prevention (OP) service delivery ability and quality and as a PRSS workforce and service system support. The PATH intervention combines (a) virtual education and (b) case-based consultation. The investigators hypothesize that PATH will improve organizational-level PRSS burnout, additional workforce outcomes, and OP service quality.

Eligibility Criteria

Survey inclusion criteria are: -Current peer recovery support specialist (PRSS) staff, including employee or volunteer, of a participating Recovery Community Organization (RCO) PRSS semi-structured qualitative interview inclusion criteria are: * Current PRSS who delivers direct, individualized peer recovery coaching services at a participating RCO, * Employed at their organization for at least 90 days. Administrator semi-structured qualitative interview inclusion criteria are: -Current administrator at a participating RCO Client semi-structured qualitative interview inclusion criteria are: * Has has service contact with the RCO at least 90 days prior to the RCO's PATH completion date * Has one or more nuanced harm reduction goals in the recovery plan (i.e., goals extending beyond basic overdose prevention) * Has received services from a PRSS participating in the post-PATH semi-structured interview

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07886944). StuddyBuddy aggregates publicly available trial information.