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Attachment-Based Family Therapy for Adolescents With Binge Eating

Attachment-Based Family Therapy for Adolescents With Transdiagnostic Binge Eating

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04779801
Acronym
ABFT
Enrollment
20
Registered
2021-03-03
Start date
2020-12-10
Completion date
2022-04-10
Last updated
2021-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Binge-Eating Disorder, Bulimia Nervosa, Other Specified Feeding or Eating Disorder

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.

Interventions

16 weeks of Attachment-Based Family Therapy treatment.

Sponsors

Drexel University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 22 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Five-Minute Speech Sample (FMSS)Change in critical comments and emotional overinvolvement from baseline to treatment completion, at 16 weeksThe Five-Minute Speech Sample is a widely-used interview to assess critical comments and emotional overinvolvement in families.

Secondary

MeasureTime frameDescription
Eating Disorder Examination (EDE)Change in frequency of binge-eating and, if applicable, purging from baseline to treatment completion, at 16 weeksThe Eating Disorder Examination is a widely-used, semi-structured interview for the assessment of eating disorder symptoms.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026