CClinicalTrials.gg
Status unknownNCT04779801ABFTUpdated Mar 3, 2021

Attachment-Based Family Therapy for Adolescents With Binge Eating

An interventional study of Attachment-Based Family Therapy in Bulimia Nervosa, Binge-Eating Disorder and Other Specified Feeding or Eating Disorder, sponsored by Drexel University. Status unknown at 1 site in United States. Open to participants aged 12 Years to 22 Years. Per ClinicalTrials.gov, last updated 2021-03-03.

Sponsored by Drexel University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2020), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
12 Years to 22 Years
Sex
All
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Study 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.

Read the 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.

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Conditions studied

  • Bulimia Nervosa
  • Binge-Eating Disorder
  • Other Specified Feeding or Eating Disorder
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In context

Bulimia

319 studies on the registry are indexed under Bulimia; 53 are open to participants now.

This study's planned enrollment of 20 is below the median of 61 across 249 interventional studies indexed under Bulimia.

Browse Bulimia studies →

Lead sponsor

Drexel University is the lead sponsor of 110 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Years to 22 Years
Sexes eligible
All
Accepts 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

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
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    ABFT

    Adolescents and one or both parents will complete 16 weeks of Attachment-Based Family Therapy treatment.

    Behavioral: Attachment-Based Family Therapy

Interventions

  • BehavioralAttachment-Based Family Therapy

    16 weeks of Attachment-Based Family Therapy treatment.

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What researchers measure

Primary outcomes

  1. Five-Minute Speech Sample (FMSS)

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

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

Secondary outcomes

  1. Eating Disorder Examination (EDE)

    The Eating Disorder Examination is a widely-used, semi-structured interview for the assessment of eating disorder symptoms.

    Time frame: Change in frequency of binge-eating and, if applicable, purging from baseline to treatment completion, at 16 weeks

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Study locations

1 of 1 sites recruiting
  • Drexel University
    Philadelphia, Pennsylvania 19104, United States
    • Sophie R Abber, B.A. · Contact · wellteen@drexel.edu · 215-553-7110
    • Stephanie M Manasse, Ph.D. · Principal investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04779801
Lead sponsor
Drexel University
Responsible party
Sponsor
First posted
Mar 3, 2021
Start date
Dec 10, 2020
Primary completion
Dec 10, 2021 (estimated)
Completion
Apr 10, 2022 (estimated)
Last update
Mar 3, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2020. You cannot join it, but the record below documents what was studied.

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