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Behavioral Intervention
Provider Training for Eating Disorders (OPTED Trial)
N/A
Waitlist Available
Led By Erin C Accurso, PhD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12-month follow-up
Awards & highlights
Summary
This trial is testing two ways of training clinicians in a family-based approach to treating restrictive eating disorders.
Who is the study for?
This trial is for licensed mental health providers in California who treat patients with Medicaid and work in a participating county. Unlicensed providers can join if they have a licensed supervisor. It's not open to students or learners.
What is being tested?
The study compares two training methods for treating restrictive eating disorders: web-based training versus live, in-person training. Mental health clinicians will be randomly assigned to one of these methods.
What are the potential side effects?
Since this trial involves professional training rather than medical treatments, traditional side effects are not applicable. However, participants may experience differences in learning effectiveness or satisfaction.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12-month follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12-month follow-up
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Family-Based Treatment Knowledge Assessment (FBT-KA) Score at Post-Training
Number of participants who complete training
Secondary study objectives
Number of participants who receive FBT consultation at 12 months
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Web-based trainingExperimental Treatment1 Intervention
Web-based training will provide online training primarily focused on family-based treatment and appropriate adaptations to the treatment model.
Group II: Live trainingActive Control1 Intervention
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.
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Who is running the clinical trial?
National Institute of Mental Health (NIMH)NIH
2,869 Previous Clinical Trials
2,777,451 Total Patients Enrolled
47 Trials studying Anorexia Nervosa
22,758 Patients Enrolled for Anorexia Nervosa
University of California, San FranciscoLead Sponsor
2,551 Previous Clinical Trials
15,257,801 Total Patients Enrolled
5 Trials studying Anorexia Nervosa
467 Patients Enrolled for Anorexia Nervosa
Erin C Accurso, PhDPrincipal InvestigatorUniversity of California, San Francisco
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Research Study Groups:
This trial has the following groups:- Group 1: Web-based training
- Group 2: Live training
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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