Personalized treatment for eating disorders
Innovations in Personalizing Treatment for Eating Disorders Using Idiographic Methods and the Impact of Personalization on Psychological, Physical, and Sociodemographic Outcomes
This study is testing a new personalized treatment for adults with eating disorders like anorexia and bulimia to see if it can help them respond better to therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 320 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | University of Louisville Academic / other |
| Locations | 1 site (Louisville, Kentucky) |
| Trial ID | NCT06208605 on ClinicalTrials.gov |
What this trial studies
This study aims to develop personalized treatment approaches for individuals suffering from eating disorders, particularly anorexia nervosa and bulimia nervosa. By utilizing Transdiagnostic Network Informed Personalized Treatment and Enhanced Cognitive Behavioral Therapy, the study seeks to improve treatment responses by considering individual social contexts and psychological needs. The goal is to address the high rates of treatment non-response and the significant burden associated with eating disorders. The study will involve participants aged 18-65 who have a current diagnosis of an eating disorder.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 with a current diagnosis of an eating disorder, excluding those with avoidant/restrictive food intake disorder (ARFID).
Not a fit: Patients experiencing active suicidality, mania, or psychosis may not benefit from this study due to the nature of their conditions.
Why it matters
Potential benefit: If successful, this study could lead to more effective and personalized treatment options for individuals with eating disorders, improving their recovery outcomes.
How similar studies have performed: While personalized treatment approaches for eating disorders are still emerging, there is a growing body of evidence suggesting that tailored interventions can improve outcomes, indicating potential success for this novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Current diagnosis of any active eating disorder except ARFID * Ages 18-65 Exclusion Criteria: * Active Suicidality * Active Mania * Active psychosis
Where this trial is running
Louisville, Kentucky
- Eating Anxiety Laboratory and Clinic — Louisville, Kentucky, United States (Recruiting)
Study contacts
- Principal investigator: Cheri A Levinson, PhD — University of Louisville
- Study coordinator: Cheri A Levinson, PhD
- Email: cheri.levinson@louisville.edu
- Phone: 502-852-7795
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.