Peer Burnout Reduction Intervention in Harm Reduction Services
This clinical trial aims to assess the acceptability, appropriateness, and feasibility of a peer burnout reduction intervention in harm reduction services. Participants will evaluate the intervention's relevance, practicality, and fit using the Acceptability, Appropriateness, and Feasibility Scales. Additionally, satisfaction with the training will be measured using a custom survey.
PATH (Peer Advanced Training in Harm reduction)
Compassion Fatigue+12
+ Occupational Stress
+ Burnout, Psychological
Services Research Study
Summary
Study start date: January 15, 2026
Actual date on which the first participant was enrolled.This study is designed to test a new program called PATH, aimed at reducing burnout among peer recovery support specialists (PRSS) working in Recovery Community Organizations (RCOs). The study involves both these specialists and their supervisors to see how well the program works, how suitable it is, and whether it can be easily implemented. The goal is to help these workers manage stress better, feel more satisfied in their roles, and improve their health-related knowledge and skills. This is important because these workers play a crucial role in supporting people recovering from substance use disorders, and reducing their stress can lead to better support for the people they help. Participants will engage in a total of 15 hours of training over three months, which includes online learning and interactive group sessions called ECHO meetings. The online modules take three hours and must be completed before the ECHO sessions, which occur weekly and involve discussions on real-life cases. Throughout the study, participants' engagement will be monitored, and they will complete surveys before and after the training to assess their experiences and measure changes in burnout and job satisfaction. There will also be focus groups and interviews to gather more detailed feedback. The study will measure the program's impact on reducing stress and improving job satisfaction among these essential workers.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.100 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * employed at a Recovery Community Organization or an organization providing direct harm reduction services, including syringe and/or outreach services * current PRSS staff or administrator involved in HR service delivery * is at least 18 years of age. Exclusion Criteria: * none
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location