N/A
N=85
Optimizing Provider Training in Eating Disorders (OPTED)
Anorexia Nervosa · Atypical Anorexia Nervosa
Bottom Line
View on ClinicalTrials.gov: NCT05389657 ↗Enrolled (actual)
85
Serious AEs
0.0%
Results posted
Aug 2025
Primary outcome: Primary: Number of Participants Who Complete Training — 48; 22; 8; 7 Participants — p=0.47
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Web-based training (Behavioral); Live training (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of California, San Francisco
- Primary completion
- Jun 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Who Complete Training |
48; 22; 8; 7 | 0.47 |
| PRIMARY Family-Based Treatment Knowledge Assessment (FBT-KA) Score at Post-Training |
20.52; 18.30 | .29 |
| SECONDARY Number of Participants Who Receive FBT Consultation at 12 Months |
28; 10; 21; 11; 7; 8 | 0.92 |
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.
Eligibility Criteria
Inclusion Criteria
- 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
Exclusion criteria
- Students (practicum students, interns, externs) or other learners
Data sourced from ClinicalTrials.gov (NCT05389657). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.