Recruiting soon

Peer Burnout Reduction Intervention in Harm Reduction Services

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

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.

What is being tested

PATH (Peer Advanced Training in Harm reduction)

Behavioral
Who is being recruted

Compassion Fatigue+12

+ Occupational Stress

+ Burnout, Psychological

Over 18 Years
See all eligibility criteria
How is the trial designed

Services Research Study

Phase 2
Interventional
Study Start: January 2026
See protocol details

Summary

Principal SponsorChestnut Health Systems
Study ContactDennis Watson, PhDMore contacts
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

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.

Official TitlePATH to Reducing Burnout Among Peers Who Deliver Harm Reduction Services: Improving Workforce and Service System Outcomes Through a Combined eLearning and Group Consultation Intervention (R61 Phase Pilot) 
Principal SponsorChestnut Health Systems
Study ContactDennis Watson, PhDMore contacts
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

100 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Compassion FatigueOccupational StressBurnout, PsychologicalNarcotic-Related DisordersBehaviorMental DisordersBehavioral SymptomsFatigueMental FatigueOpioid-Related DisordersSigns and SymptomsStress, PsychologicalPathological Conditions, Signs and SymptomsSubstance-Related DisordersChemically-Induced Disorders

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.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Receive PATH pilot intervention

Study 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

Suspended

Chestnut Health Systems Lighthouse Institute

Chicago, United StatesSee the location
Recruiting soonOne Study Center