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SuperAssist: Client-Centered Supervision Assist App for Mental Health Providers

NCT07247045 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2026-05-07

No results posted yet for this study

Summary

The goal of this pilot study is to test a Supervision Assist App (SuperAssist) for implementing Client-Centered Supervision (CCS) to improve supervision practices for mental health providers (providers). During previous Aims 1 and 2, a SuperAssist beta version was designed and developed before beta testing of SuperAssist with providers and supervisors. During this pilot randomized controlled trial (Aim 3), the investigators will evaluate the feasibility, preliminary outcomes, and change mechanisms of SuperAssist.

Conditions

  • Behavioral Health Client-centered Supervision

Interventions

OTHER

Client-centered supervision training and use of a mobile app

Behavioral health staff will learn how to implement client-centered practice and supervision with SuperAssist (Supervision Assist App). SuperAssist is designed to facilitate supervision practices around clients' identified goals and needs, which may positively impact clinician job well-being (e.g., burnout, job satisfaction), professional growth, the quality of care, and eventually client outcomes.

Sponsors & Collaborators

  • National Institute of Mental Health (NIMH)

    collaborator NIH

  • Indiana University

    lead OTHER

Principal Investigators

  • Sadaaki Fukui, PhD, MSW, MA · Indiana University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-01
Primary Completion
2026-10-31
Completion
2026-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07247045 on ClinicalTrials.gov