Impact of Stress First Aid for Workers in Substance Misuse Settings

NCT ID: NCT07177014

Last Updated: 2025-10-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

500 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-01

Study Completion Date

2029-02-28

Brief Summary

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Test the effectiveness of SFA adapted for the harm reduction workforce (SFA/HRW) compared to a no treatment control condition on social-support and burnout of HRWs in a cluster-randomized hybrid type I trial.

Detailed Description

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Conditions

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Occupational Health

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Cluster-randomized hybrid type I trial of SFA adapted for the harm reduction workforce (SFA/HRW) compared to a no treatment control condition.
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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No Treatment

Control: No Treatment

Group Type NO_INTERVENTION

No interventions assigned to this group

Stress First Aid for Harm Reduction Workers

Treatment group receives Stress First Aid for Harm Reduction Workers, a 2-hour training and up to six virtual 30-minute monthly learning collaborative meetings.

Group Type EXPERIMENTAL

Stress First Aid for Harm Reduction Workers (SFA/HRW)

Intervention Type BEHAVIORAL

Stress First Aid for Harm Reduction Workers is a 2-hour training and up to six virtual 30-minute monthly learning collaborative meetings.

Interventions

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Stress First Aid for Harm Reduction Workers (SFA/HRW)

Stress First Aid for Harm Reduction Workers is a 2-hour training and up to six virtual 30-minute monthly learning collaborative meetings.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* At least 18 years of age
* Employed in a paid role as a harm reduction worker or community health/outreach worker (whose work includes harm reduction) with people who use drugs within TX, LA, AR, OK, NM and tribal areas
* Able and willing to provide informed consent

Exclusion Criteria

\- Inability to provide consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

University of Texas at Austin

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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R61DA059887

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY00008024

Identifier Type: -

Identifier Source: org_study_id

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