RECRUITING

Targeting Social Function to Improve Outcomes in Eating Disorders

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Targeting Social Function to Improve Outcomes in Eating Disorders

Quick Facts

Study Start:2024-02-28
Study Completion:2028-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06198023

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 30 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * DSM-5 criteria met for Anorexia Nervosa (AN), Atypical Anorexia Nervosa (AAN), Bulimia Nervosa (BN), Purging Disorder (PD), or subthreshold Bulimia Nervosa within the past twelve months
  1. * Current inpatient or residential treatment
  2. * Medical instability or safety/suicide risk as determined by the PI

Contacts and Locations

Study Contact

Ava Ryan
CONTACT
214-648-4617
edresearch@utsouthwestern.edu

Principal Investigator

Carrie J McAdams, MD PhD
PRINCIPAL_INVESTIGATOR
University of Texas Southwestern Medical Center

Study Locations (Sites)

UT Southwestern Multispecialty Psychiatry Clinic
Dallas, Texas, 75247
United States

Collaborators and Investigators

Sponsor: University of Texas Southwestern Medical Center

  • Carrie J McAdams, MD PhD, PRINCIPAL_INVESTIGATOR, University of Texas Southwestern Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-28
Study Completion Date2028-09

Study Record Updates

Study Start Date2024-02-28
Study Completion Date2028-09

Terms related to this study

Keywords Provided by Researchers

  • social function
  • social cognition
  • social processing
  • psychoeducation
  • group therapy
  • group intervention
  • art therapy

Additional Relevant MeSH Terms

  • Eating Disorders
  • Anorexia Nervosa
  • Bulimia Nervosa
  • Atypical Anorexia Nervosa
  • Purging (Eating Disorders)
  • Other Specified Feeding or Eating Disorder