UCAN: Uniting Couples in the Treatment of Anorexia Nervosa

Not Applicable

Completed

• Conditions: Anorexia Nervosa

• Registration Number: NCT00928109
• Lead Sponsor: University of North Carolina, Chapel Hill

Brief Summary

UCAN is a research program funded by the National Institute of Mental Health and is part of the UNC Eating Disorders Program. UCAN aims to help couples work together in the treatment of anorexia nervosa. Couples participate in UCAN over a period of six months and return for follow-up treatment three months after the end of the original six-month period. Patients receive weekly individual therapy, monthly psychiatry consultations, monthly dietary consultations in addition to being randomized to one of two types of weekly couples therapy. Participation in UCAN can help participants gain new confidence in facing anorexia as a team and can help us understand how best to involve partners in the treatment of eating disorders.

Detailed Description

Patients receive comprehensive eating disorder treatment at the UNC Eating Disorders Outpatient Program in addition to couples therapy. Eligibility: Participants may be eligible if they are 18 or older, have anorexia nervosa and are currently living with a partner with whom they have been in a committed relationship for at least a year. The partner must also be willing to enter treatment.

Study Timeline

• Study Start: 2008-04
• Study First Submitted: 2009-06-23
• Study First Submitted QC: 2009-06-24
• Study First Posted: 2009-06-25
• Primary Completion: 2012-06
• Study Completion: 2012-06
• Status Verified: 2012-11
• Last Update Submitted: 2012-11-08
• Last Update Posted: 2012-11-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Anorexia Nervosa,
• 18 years or older,
• BMI 16 or higher,
• In a committed relationship with a partner for 1 year or longer and currently living together.

Exclusion Criteria

• Alcohol or drug dependence in past year,
• Current significant suicidal ideation,
• Developmental disability that would impair the ability of the participant to benefit from the intervention,
• Psychosis,
• BMI less than 16.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Eating disorder behavior	9 months

Secondary Outcome Measures

Name	Time	Method
Couple Satisfaction	9 months

Trial Locations

Locations (1)

UNC Chapel Hill; 🇺🇸 Chapel Hill, North Carolina, United States