SuperAssist: Client-Centered Supervision Assist App for Mental Health Providers
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Indiana University
- Study ID
- NCT07247045
- Status
- Enrolling By Invitation
Conditions
- Behavioral Health Client-centered Supervision
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Client-centered supervision training and use of a mobile app — OTHERBehavioral 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.
Study Details
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.
Key Dates
- Start date
- Apr 1, 2026
- Status verified
- May 2026
- Primary completion
- Oct 31, 2026
- Completion
- Oct 31, 2026
Study Design
- Enrollment
- 180 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- HEALTH_SERVICES_RESEARCH
Arms
- Experimental: SuperAssist Group-Behavioral Health StaffClient-centered supervision training and use of a mobile app for behavioral health staff
- No Intervention: Control Group-Behavioral Health Staff
- Experimental: SuperAssist Group-ClientsClients of behavioral health staff assigned to the Experimental Arm
- No Intervention: Control Group-ClientsClients of behavioral health staff assigned to the Control Arm
Primary Outcome Measure
Change from Baseline Perception of Supervisory Support (PSS) Scale at 3 months [ Time Frame: measured with staff at 3 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Places for People | St Louis | Missouri | 63118 | - |
Find similar trials in St Louis, MO
By research site