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Clinical Trials/NCT04779801
NCT04779801
Unknown
N/A

Attachment-Based Family Therapy for Adolescents With Transdiagnostic Binge Eating

Drexel University1 site in 1 country20 target enrollmentDecember 10, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Bulimia Nervosa
Sponsor
Drexel University
Enrollment
20
Locations
1
Primary Endpoint
Five-Minute Speech Sample (FMSS)
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to examine whether Attachment-Based Family Therapy (ABFT), a well-validated treatment for adolescents with depression and suicidality, is feasible and acceptable for adolescents with binge eating and their families.

Detailed Description

This study involves a phone screen and baseline assessment to determine eligibility. Participants who are eligible for the study will receive 16 weeks of ABFT treatment. The treatment primarily focuses on improving communication and relationships within the family, and will also address disordered eating behaviors (e.g., binge eating, laxative use, self-induced vomiting). All participants enrolled in the study will receive the same treatment. Participants will also complete research assessments throughout treatment, at the end of treatment, and 3-months after the end of treatment. Research assessments include a battery of questionnaires and interviews.

Registry
clinicaltrials.gov
Start Date
December 10, 2020
End Date
April 10, 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Speak, write, and understand English
  • Age 12-22 years old
  • Have a diagnosis of DSM-5 AN, BN, BED, or OSFED
  • Medically stable for outpatient treatment
  • Must have a parent, guardian, or primary caregiver who is willing to participate in the study and treatment

Exclusion Criteria

  • Acute suicide risk
  • No parent or guardian agreement to participate
  • Are currently receiving psychological treatment for an eating disorder
  • Are currently receiving weight loss treatment
  • Co-morbid clinically significant psychological disorder that would require attention beyond the study treatment (e.g., psychotic disorder, substance dependence)
  • Diagnosis of intellectual disability

Outcomes

Primary Outcomes

Five-Minute Speech Sample (FMSS)

Time Frame: Change in critical comments and emotional overinvolvement from baseline to treatment completion, at 16 weeks

The Five-Minute Speech Sample is a widely-used interview to assess critical comments and emotional overinvolvement in families.

Secondary Outcomes

  • Eating Disorder Examination (EDE)(Change in frequency of binge-eating and, if applicable, purging from baseline to treatment completion, at 16 weeks)

Study Sites (1)

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