Actively Recruiting

Phase Not Applicable
Age: 12Years - 18Years
All Genders
NCT05763849

Interoceptive Exposure for Adolescents With Low Weight Eating Disorders

Led by Icahn School of Medicine at Mount Sinai · Updated on 2025-06-04

120

Participants Needed

1

Research Sites

250 weeks

Total Duration

On this page

Sponsors

I

Icahn School of Medicine at Mount Sinai

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This project includes a parallel group randomized controlled trial comparing two psychological treatments: 1) Exposure-based Family Therapy (IE) vs. 2) Family Based Therapy (FBT) for low weight eating disorders with 12 month follow-up. Primary outcomes are expected body weight and clinical impairment. Three mechanisms of change (Autonomous Eating, Non-Judgmental Body Awareness, and Extinction Learning) will be examined in a process mediation models of change.

CONDITIONS

Official Title

Interoceptive Exposure for Adolescents With Low Weight Eating Disorders

Who Can Participate

Age: 12Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 12 to 18 years
  • Speak English
  • Permission from pediatrician or equivalent to receive outpatient care
  • Clinically significant restriction of food intake by EDA-5 or evidence of persistent food avoidance from patient or guardians
  • Inability to maintain greater than minimally low body weight based on BMI for age percentiles and growth trajectories
Not Eligible

You will not qualify if you...

  • Comorbid psychotic or bipolar disorder
  • Active suicidal ideation
  • Current substance dependence
  • Psychiatric medication initiated or dosage changes less than 2 weeks from baseline
  • Major medical illness such as diabetes mellitus or Crohn's disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Psychiatry, Eating and Weight Disorders Program

New York, New York, United States, 10028

Actively Recruiting

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Research Team

T

Thomas Hildebrandt, Psy.D.

CONTACT

J

Jessica Bibeau, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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