Improving social function in individuals with eating disorders
Targeting Social Function to Improve Outcomes in Anxiety and Eating Disorders
This study is testing two different treatments to see if they can help people with eating disorders improve their social skills and overall well-being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 30 Years |
| Sex | All |
| Sponsor | University of Texas Southwestern Medical Center Academic / other |
| Locations | 1 site (Dallas, Texas) |
| Trial ID | NCT06198023 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates two therapeutic interventions aimed at enhancing social function in patients with eating disorders. Participants will receive either educational or interactive treatment, with the latter including a collaborative art task. The study involves baseline assessments, eight treatment sessions over 12 weeks, and follow-up evaluations at 4, 8, and 12 months. The goal is to determine the effectiveness of these interventions in improving clinical outcomes related to eating disorders and associated anxiety.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18-30 who have met DSM-5 criteria for an eating disorder or anxiety disorder in the past year.
Not a fit: Patients currently in inpatient or residential treatment or those deemed medically unstable or at risk for suicide may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved social functioning and overall clinical outcomes for patients with eating disorders.
How similar studies have performed: Previous pilot studies targeting social function in eating disorders have shown clinical improvements, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * In the past 12 months, has met DSM-5 criteria met 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 18-30 Exclusion Criteria: * Current inpatient or residential treatment * Medical instability or safety/suicide risk as determined by the PI
Where this trial is running
Dallas, Texas
- UT Southwestern Multispecialty Psychiatry Clinic — Dallas, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Carrie J McAdams, MD PhD — University of Texas Southwestern Medical Center
- Study coordinator: Ava Ryan
- Email: edresearch@utsouthwestern.edu
- Phone: 214-648-4617
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.