Eating Disorder Clinical Trial
Official title:
Treatment Outcome in Eating Disorders
NCT number | NCT03599921 |
Other study ID # | 47919 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | May 6, 2015 |
Est. completion date | January 1, 2021 |
Verified date | July 2021 |
Source | Children's Hospitals and Clinics of Minnesota |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Do the current eating disorder treatments, i.e., Family-based Treatment (FBT) and Enhanced Cognitive behavioral therapy (CBT-E), offered at the Center for the Treatment of Eating Disorders (CTED) demonstrate effectiveness? Specifically, which type of treatment is most effective for which diagnoses? Participants with Anorexia Nervosa (AN), Bulimia Nervosa (BN), Other Specified Feeding or Eating Disorder (OSFED), or Unspecified Feeding or Eating Disorder (UFED) in this study will self select one of the two treatment groups, FBT or CBT-E. Additionally, does Family-based Treatment (FBT) modified for Avoidant/Restrictive Food Intake Disorder (ARFID) and Family-based Treatment (FBT) combined with the Unified Protocol (UP) for Transdiagnostic Treatment of Emotional Disorders (FBT+UP for ARFID) demonstrate effectiveness for patients with an Avoidant/Restrictive Food Intake Disorder (ARFID) diagnosis?
Status | Completed |
Enrollment | 275 |
Est. completion date | January 1, 2021 |
Est. primary completion date | January 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 6 Years and older |
Eligibility | Inclusion Criteria: - Patients must be at least 6 years of age, attending the CTED clinic for outpatient treatment of a Diagnostic and Statistical Manual, 5th Edition (DSM-5) diagnosed eating disorder in order to be included in this study. Exclusion Criteria: - Participants who are receiving inpatient services only and will not return to CTED for outpatient treatment. - Participants with a co-morbid medical disorder known to influence eating or weight. - Participants presenting with a significant psychotic disorder. - Participants who are acutely suicidal. - Participants who demonstrate significant substance abuse and/or substance dependence. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Children's Hospitals and Clinics of Minnesota | University of California, San Francisco |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Therapy effectiveness | 1) Evaluate which therapies work effectively for the treatment of eating disorders, and which types of treatments are most effective for specific diagnoses. | Measured at end of treatment (an average of 6-9 months) and at 6 and 12 month follow-up. | |
Secondary | Treatment moderators | 1) Explore predictors and moderators of treatment outcome. | Measured at end of treatment (an average of 6-9 months) and at 6 and 12 month follow-up. |
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