Optimizing Provider Training in Eating Disorders (OPTED)
OPTED
Dissemination and Implementation of Family-Based Treatment in Publicly-Funded Clinics: Optimizing Provider Training in Eating Disorders (OPTED)
1 other identifier
interventional
85
1 country
1
Brief Summary
This is a randomized controlled trial for mental health clinicians comparing two methods of training in family-based treatment (FBT) for restrictive eating disorders.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 18, 2022
CompletedFirst Posted
Study publicly available on registry
May 25, 2022
CompletedStudy Start
First participant enrolled
July 14, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 3, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 3, 2024
CompletedResults Posted
Study results publicly available
August 7, 2025
CompletedAugust 7, 2025
July 1, 2025
1.9 years
May 18, 2022
June 27, 2025
July 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Number of Participants Who Complete Training
Training completion will be the number of participants who complete the full course of training.
Post-training (measured at the time of planned completion, which will be 10 weeks from the start of web-based training, or on the second day of live training)
Family-Based Treatment Knowledge Assessment (FBT-KA) Score at Post-Training
The FBT Knowledge Assessment (FBT-KA) is an 28-item multiple-choice test that measures knowledge about FBT. Scores range from 0 to 28, with higher scores indicating more knowledge.
Baseline and post-training (measured immediately following completion of training)
Secondary Outcomes (1)
Number of Participants Who Receive FBT Consultation at 12 Months
12-month follow-up (measured at 12 months from the deadline for completion of training)
Study Arms (2)
Web-based training
EXPERIMENTALWeb-based training will provide online training primarily focused on family-based treatment and appropriate adaptations to the treatment model.
Live training
ACTIVE COMPARATORLive training will include two days of expert-led live training (via zoom). The content of the training will be similar to that provided in web-based training, primarily focused on family-based treatment and appropriate adaptations to the treatment model.
Interventions
Web-based training will be divided into training modules that will be completed by participants over the course of 6-8 weeks. Training will include didactic training videos, knowledge checks, example sessions, and a library of resources.
The live training will be delivered by two trainers over the course of two days via Zoom.
Eligibility Criteria
You may qualify if:
- Mental health provider licensed to practice in the state of California, or unlicensed mental health providers in California who are formally employed by their agency/clinic and have a licensed clinical supervisor who agrees to take legal responsibility for any cases treated with FBT
- Must treat patients with Medicaid insurance in a participating county
You may not qualify if:
- \- Students (practicum students, interns, externs) or other learners
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of California, San Francisco
San Francisco, California, 94103, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Erin Accurso
- Organization
- University of California, San Francisco
Study Officials
- PRINCIPAL INVESTIGATOR
Erin C Accurso, PhD
University of California, San Francisco
Publication Agreements
- PI is Sponsor Employee
- Yes
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 18, 2022
First Posted
May 25, 2022
Study Start
July 14, 2022
Primary Completion
June 3, 2024
Study Completion
June 3, 2024
Last Updated
August 7, 2025
Results First Posted
August 7, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share