NCT07218562

Brief Summary

The investigators propose to develop and 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
18

participants targeted

Target at below P25 for phase_2

Timeline
Completed

Started Jan 2026

Shorter than P25 for phase_2

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 30, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

October 20, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

January 12, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 8, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 8, 2026

Completed
5 months until next milestone

Results Posted

Study results publicly available

October 2, 2026

Completed
Last Updated

October 2, 2026

Status Verified

September 1, 2026

Enrollment Period

4 months

First QC Date

September 30, 2025

Results QC Date

August 10, 2026

Last Update Submit

September 9, 2026

Conditions

Keywords

peer recovery support specialistopioid use disordersubstance use disorderoverdose prevention

Outcome Measures

Primary Outcomes (4)

  • Acceptability, Appropriateness, and Feasibility

    Measured using the Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM), and Feasibility of Intervention Measure (FIM), 12 validated items measuring participants' level of agreement (1/Completely disagree - 5/Completely agree) with the intervention's relevance, practicality, and fit for their work. Each of the three scales (AIM, IAM, and FIM) contains 4 questions and is scored by averaging responses. Each has a minimum score of 1 and a maximum score of 5. Higher scores indicate higher perceived levels of Acceptability, Appropriateness, or Feasibility of the intervention.

    At the conclusion of PATH eLearning modules, approximately 1 month post-baseline

  • Acceptability, Appropriateness, and Feasibility

    Measured using the Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM), and Feasibility of Intervention Measure (FIM), 12 validated items measuring participants' level of agreement (1/Completely disagree - 5/Completely agree) with the intervention's relevance, practicality, and fit for their work. Each of the three scales (AIM, IAM, and FIM) contains 4 questions and is scored by averaging responses. Each has a minimum score of 1 and a maximum score of 5. Higher scores indicate higher perceived levels of Acceptability, Appropriateness, or Feasibility of the intervention.

    At the conclusion of PATH ECHO sessions, approximately 3 months post-baseline

  • Training Satisfaction

    Measured using the Training Satisfaction Questionnaire, a custom 5-point Likert-scale (1/Totally disagree - 5/Totally agree) survey with 12-items assessing overall satisfaction with the learning experience, content relevance, and applicability to peer support practice. The questionnaire includes 3 sub-scales: Objectives and Content (3 items), Methods and Training Context (6 items), and Usefulness and Overall Rating (3 items). Each sub-scale is scored by averaging responses and has a minimum score of 1 and a maximum score of 5. Higher scores indicate higher levels of satisfaction with the training.

    At the conclusion of PATH eLearning modules, approximately 1 month post-baseline

  • Training Satisfaction

    Measured using the Training Satisfaction Questionnaire, a custom 5-point Likert-scale (1/Totally disagree - 5/Totally agree) survey with 12-items assessing overall satisfaction with the learning experience, content relevance, and applicability to peer support practice. The questionnaire includes 3 sub-scales: Objectives and Content (3 items), Methods and Training Context (6 items), and Usefulness and Overall Rating (3 items). Each sub-scale is scored by averaging responses and has a minimum score of 1 and a maximum score of 5. Higher scores indicate higher levels of satisfaction with the training.

    At the conclusion of PATH ECHO sessions, approximately 3 months post-baseline

Secondary Outcomes (18)

  • Job Crafting

    Baseline

  • Job Crafting

    At the conclusion of PATH eLearning modules, approximately 1 month post-baseline

  • Job Crafting

    At the conclusion of PATH ECHO sessions, approximately 3 months post-baseline

  • Overdose Prevention Knowledge, Attitudes, and Skills

    Baseline

  • Overdose Prevention Knowledge, Attitudes, and Skills

    At the conclusion of PATH eLearning modules, approximately 1 month post-baseline

  • +13 more secondary outcomes

Study Arms (1)

PATH pilot participants

EXPERIMENTAL

Receive PATH pilot intervention

Behavioral: PATH (Peer Advanced Training for total Health)

Interventions

PATH is 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. PATH will include 4 hours of eLearning modules completed within a 1-month period, as well as 8 weekly ECHO sessions lasting 1.5 hours each delivered over 2 months. Each ECHO session includes a 30-minute presentation followed by one hour of case-based discussion about a real client or problem. The entire PATH intervention will take 16 hours (4 hours of eLearning and 12 hours of ECHO participation) over 3 months. Participants are expected to complete all 16 hours, completing the 4 hours of eLearning before starting the 12 hours of ECHO activities.

PATH pilot participants

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • current PRSS staff or administrator employed by a partnering Recovery Community Organization (RCO)
  • is at least 18 years of age.

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chestnut Health Systems Lighthouse Institute

Chicago, Illinois, 60610, United States

Location

MeSH Terms

Conditions

Burnout, PsychologicalCompassion FatigueOpioid-Related DisordersSubstance-Related Disorders

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehaviorMental FatigueFatigueSigns and SymptomsPathological Conditions, Signs and SymptomsOccupational StressNarcotic-Related DisordersChemically-Induced DisordersMental Disorders

Results Point of Contact

Title
Dennis Watson
Organization
Chestnut Health Systems

Study Officials

  • Dennis P Watson, PhD

    Chestnut Health Systems

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
phase 2
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior Research Scientist

Study Record Dates

First Submitted

September 30, 2025

First Posted

October 20, 2025

Study Start

January 12, 2026

Primary Completion

May 8, 2026

Study Completion

May 8, 2026

Last Updated

October 2, 2026

Results First Posted

October 2, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will share

De-identified individual and aggregate PRSS survey data (raw and recoded) will be shared publicly after completing all data and analyses. Files will be shared in the format most relevant to the software used to develop them, as well as CSV files. De-identified qualitative transcripts will be maintained and shared only with an established data-sharing agreement. Files containing coding lists and summaries and transcript attributes will also be shared with appropriate agreements in place. Open sharing of qualitative data may risk identifying participants, particularly in small rural organizations where contextual details are difficult to mask. Standard protections, like de-identification and Certificates of Confidentiality, may be insufficient.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Access Criteria
The study protocol, statistical analysis plan, and informed consent form will be made publicly available on Open Science Framework.

Locations