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Optimizing Provider Training in Eating Disorders (OPTED)

NCT05389657 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 85

Last updated 2025-08-07

Study results available
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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.

Conditions

  • Anorexia Nervosa
  • Atypical Anorexia Nervosa

Interventions

BEHAVIORAL

Web-based training

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.

BEHAVIORAL

Live training

The live training will be delivered by two trainers over the course of two days via Zoom.

Sponsors & Collaborators

Principal Investigators

  • Erin C Accurso, PhD · University of California, San Francisco

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-14
Primary Completion
2024-06-03
Completion
2024-06-03

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT05389657 on ClinicalTrials.gov