NCT05389657

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
85

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 25, 2022

Completed
2 months until next milestone

Study Start

First participant enrolled

July 14, 2022

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 3, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 3, 2024

Completed
1.2 years until next milestone

Results Posted

Study results publicly available

August 7, 2025

Completed
Last Updated

August 7, 2025

Status Verified

July 1, 2025

Enrollment Period

1.9 years

First QC Date

May 18, 2022

Results QC Date

June 27, 2025

Last Update Submit

July 17, 2025

Conditions

Keywords

TrainingEating disordersFamily based treatmentMedicaidCommunity mental healthChildren and adolescentsMental health clinicians

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

EXPERIMENTAL

Web-based training will provide online training primarily focused on family-based treatment and appropriate adaptations to the treatment model.

Behavioral: Web-based training

Live training

ACTIVE COMPARATOR

Live 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.

Behavioral: Live training

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.

Web-based training
Live trainingBEHAVIORAL

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

Live training

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Anorexia NervosaFeeding and Eating Disorders

Condition Hierarchy (Ancestors)

Mental DisordersSigns and Symptoms, DigestiveSigns and SymptomsPathological Conditions, Signs and Symptoms

Results Point of Contact

Title
Erin Accurso
Organization
University of California, San Francisco

Study Officials

  • Erin C Accurso, PhD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

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

Locations