Optimizing Fidelity to Family-Based Treatment for Adolescent Anorexia Nervosa
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT02139462 |
Recruitment Status :
Completed
First Posted : May 15, 2014
Last Update Posted : October 5, 2017
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Condition or disease | Intervention/treatment | Phase |
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Online Training for Therapists | Other: Standard FBT training Other: Novel FBT training | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 47 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Health Services Research |
Official Title: | Optimizing Fidelity to Family-Based Treatment for Adolescent Anorexia Nervosa |
Study Start Date : | May 2015 |
Actual Primary Completion Date : | September 2017 |
Actual Study Completion Date : | September 2017 |
Arm | Intervention/treatment |
---|---|
Experimental: Standard training
Therapists will receive standard training in FBT.
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Other: Standard FBT training
Therapists will receive standard training in Family Based Treatment (FBT) |
Experimental: Novel training
Therapists will receive a novel, more efficient training in FBT
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Other: Novel FBT training
Therapists will receive a novel training in Family Based Treatment (FBT) |
- Feasibility [ Time Frame: end of treatment (approximately 1.5 years after beginning training) ]The primary outcome will be feasibility (e.g., recruitment, attrition, assessment battery, resource costs) to conduct a sufficiently powered comparative study.
- Fidelity [ Time Frame: Session 4, end of training (approximately 1.5 years after beginning training) ]Secondary outcomes include exploring differences in therapist fidelity and relationships between fidelity and patient outcomes between these two groups (e.g., fidelity and weight change at session 4).

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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- masters or doctoral training in their field (psychology, psychiatry, family therapy).
- must be licensed
- have no reports of malpractice or loss of privileges at clinical institution
- minimum caseload 5 adolescents with AN each year over past 3 years
- no previous training in FBT
- computer/web access
Exclusion Criteria:
- Previous FBT training for AN

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02139462
United States, California | |
Stanford University | |
Stanford, California, United States, 94305 |
Principal Investigator: | James Lock, MD, PhD | Stanford University | |
Principal Investigator: | Daniel Le Grange, PhD | University of California, San Francisco | |
Principal Investigator: | W. Stewart Agras, MD | Stanford University |
Responsible Party: | James Dale Lock, Principal Investigator, Stanford University |
ClinicalTrials.gov Identifier: | NCT02139462 |
Other Study ID Numbers: |
1R21MH096779-01 ( U.S. NIH Grant/Contract ) SPO 103420 ( Other Grant/Funding Number: NIH ) |
First Posted: | May 15, 2014 Key Record Dates |
Last Update Posted: | October 5, 2017 |
Last Verified: | October 2017 |
FBT, fidelity, training |
Anorexia Anorexia Nervosa Signs and Symptoms, Digestive Feeding and Eating Disorders Mental Disorders |