Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
NCT06198023

Targeting Social Function in Anxiety and Eating Disorders

Led by University of Texas Southwestern Medical Center · Updated on 2026-05-05

60

Participants Needed

1

Research Sites

235 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Social processing and cognition are often altered in patients with eating disorders. The goal of this clinical trial is to assess two different social therapeutic interventions -- one educational, one interactive -- for their effectiveness in improving clinical outcomes in patients with eating disorders. Patients in both interventions will receive education about social function in eating disorders, but those in the interactive treatment group will complete an additional collaborative art task. Participants will: * attend a baseline study visit to complete clinical interviews, cognitive testing, and behavioral tasks * complete a pre-intervention assessment with questionnaires * attend eight sessions of their assigned treatment group over the course of 12 weeks * complete three virtual follow-up assessments 4, 8, and 12 months from their baseline * attend a final study visit to repeat some clinical interviews, cognitive testing, and behavioral tasks Researchers will compare changes in eating disorder, mood, and anxiety symptoms as well as test results from baseline and final study visits for each group to see if * patients can be treated effectively with education alone or if an interactive group component produces additional benefits * cognitive and behavioral task performance are associated with recovery or illness state.

CONDITIONS

Official Title

Targeting Social Function in Anxiety and Eating Disorders

Who Can Participate

Age: 18Years - 30Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Met DSM-5 criteria in the past 12 months for an eating disorder (Anorexia Nervosa, Atypical Anorexia Nervosa, Bulimia Nervosa, Avoidant-Restrictive Food Intake Disorder, or Other Specified Feeding or Eating Disorder) and/or an anxiety disorder (Generalized Anxiety Disorder, Social Anxiety Disorder)
  • Between the ages of 18 and 30 years
Not Eligible

You will not qualify if you...

  • Currently receiving inpatient or residential treatment
  • Medical instability or safety/suicide risk as determined by the principal investigator

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

UT Southwestern Multispecialty Psychiatry Clinic

Dallas, Texas, United States, 75247

Actively Recruiting

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Research Team

A

Ava Ryan

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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