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Optimizing Provider Training in Eating Disorders (OPTED) (OPTED)

Primary Purpose

Anorexia Nervosa, Atypical Anorexia Nervosa

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Web-based training
Live training
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Anorexia Nervosa focused on measuring Training, Eating disorders, Family based treatment, Medicaid, Community mental health, Children and adolescents, Mental health clinicians

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • University of California, San Francisco

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Web-based training

Live training

Arm Description

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

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.

Outcomes

Primary Outcome Measures

Number of participants who complete training
Training completion will be the number of participants who complete the full course of training.
Change in Family-Based Treatment Knowledge Assessment (FBT-KA) Score at Post-Training
The FBT Knowledge Assessment (FBT-KA) is an 18-item multiple-choice test that measures knowledge about FBT. Scores range from 0 to 18, with higher scores indicating more knowledge. Change will be examined from baseline (pre-training) to post-training.

Secondary Outcome Measures

Number of participants who receive FBT consultation at 12 months
Providers will report on their receipt (yes/no) of FBT-specific consultation in the 12 months following completion of training.

Full Information

First Posted
May 18, 2022
Last Updated
September 20, 2023
Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT05389657
Brief Title
Optimizing Provider Training in Eating Disorders (OPTED)
Acronym
OPTED
Official Title
Dissemination and Implementation of Family-Based Treatment in Publicly-Funded Clinics: Optimizing Provider Training in Eating Disorders (OPTED)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 14, 2022 (Actual)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
February 28, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.
Detailed Description
This is a randomized controlled trial for mental health clinicians comparing two methods of training in family-based treatment (FBT) for restrictive eating disorders. Clinicians who treat youth and accept Medicaid insurance within a predetermined group of participating California counties will be randomized to receive either web-based training (WBT) or live two-day training in FBT. Data will be collected on the feasibility, acceptability, appropriateness, and effectiveness of the training (web-based vs. live). Following training, a subset of clinicians may opt into group consultation for one year. Consultation groups will be kept separate by training condition. Data will also be collected from clinicians on the extent to which they perceive the treatment itself (i.e., FBT) as feasible, acceptable, and appropriate for Medicaid-insured youth. In addition to implementation outcomes, de-identified clinical data will be collected from providers about their cases up to one year following the initial training.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anorexia Nervosa, Atypical Anorexia Nervosa
Keywords
Training, Eating disorders, Family based treatment, Medicaid, Community mental health, Children and adolescents, Mental health clinicians

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
85 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Web-based training
Arm Type
Experimental
Arm Description
Web-based training will provide online training primarily focused on family-based treatment and appropriate adaptations to the treatment model.
Arm Title
Live training
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Web-based training
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Live training
Intervention Description
The live training will be delivered by two trainers over the course of two days via Zoom.
Primary Outcome Measure Information:
Title
Number of participants who complete training
Description
Training completion will be the number of participants who complete the full course of training.
Time Frame
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)
Title
Change in Family-Based Treatment Knowledge Assessment (FBT-KA) Score at Post-Training
Description
The FBT Knowledge Assessment (FBT-KA) is an 18-item multiple-choice test that measures knowledge about FBT. Scores range from 0 to 18, with higher scores indicating more knowledge. Change will be examined from baseline (pre-training) to post-training.
Time Frame
Baseline and post-training (measured immediately following completion of training)
Secondary Outcome Measure Information:
Title
Number of participants who receive FBT consultation at 12 months
Description
Providers will report on their receipt (yes/no) of FBT-specific consultation in the 12 months following completion of training.
Time Frame
12-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erin C Accurso, PhD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94103
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Optimizing Provider Training in Eating Disorders (OPTED)

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