NCT Number: NCT00417521
Open Trial of Family-Based Treatment for Anorexia Nervosa
This trial seeks to investigate the feasibility and effectiveness of delivering a newly manualized family-based treatment for adolescents with anorexia nervosa
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Conditions
Age range
12 year–17 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
About this study
This open trial seeks to investigate the feasibility and effectiveness of delivering a newly manualized family-based treatment for adolescents with anorexia nervosa at a site beyond the treatment's origin. Adolescents ages 12-17 with anorexia nervosa or subthreshold anorexia nervosa were treated with up to one year of this approach.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Age 12-17
- Diagnosis of full or subthreshold anorexia nervosa
- At least one parent or guardian willing to participate in treatment
Exclusion criteria
- Bipolar Disorder, Psychotic Disorder, Substance Dependence
- Mental Retardation
- Acute suicidal risk
- Acute or unstable, poorly controlled chronic medical illness
- Weight below 75% ideal body weight
Treatment and study plan
Primary outcomes
-
weight
Time frame: end of treatment
Sponsors and collaborators
Lead sponsor
New York State Psychiatric Institute
Other
Registry information
Official study title
Pilot Study of Manualized Family Therapy for Adolescents With Anorexia Nervosa
Important dates
- Study start
- 2004
- Primary completion
- 2008
- Study completion
- 2008
- First posted
- Jan 1, 2007
- Registry last updated
- Sep 26, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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