Long-term study on eating disorders
Official title: PROspective Longitudinal All-comer Inclusion Study in Eating Disorders
Run by Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg Hospital · NCT03224091 · Data updated 2026-11-12
This study is trying to understand eating disorders like Anorexia and Bulimia by looking at patients over time to find clues that could help improve treatments.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg Hospital Academic / other |
| Locations | 1 site (Ballerup Municipality, Capitol Region) |
| Status | Recruiting |
| Started | January 25, 2016 |
| Main results expected | April 1, 2030 |
| Study ends | April 1, 2030 |
| Registry record updated | April 7, 2022 |
| Trial ID | NCT03224091 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals diagnosed with an eating disorder as per ICD-10 criteria.
✕Probably not a fit
Patients who are under forced care or non-voluntary treatment may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The PROLED study is a prospective and longitudinal examination of patients with various eating disorders, including Anorexia Nervosa and Bulimia Nervosa. It involves annual interviews, qualitative assessments, and the collection of biological samples such as blood, urine, and feces to better understand the psychopathology and pathophysiology of these conditions. The study aims to identify biomarkers that could inform prognosis and treatment responses, addressing the significant unmet medical needs in this area. By analyzing the data collected, researchers hope to uncover novel molecular targets for future treatments.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and treatment options for patients with eating disorders.
How similar studies have gone: While the study's approach is comprehensive, similar studies have shown promise in understanding the biological underpinnings of eating disorders, suggesting potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Eating Disorder (ICD-10) Exclusion Criteria: * Forced care/non-voluntary
Where it's running
-
Mental Health Center
Ballerup Municipality, Capitol Region, Denmark Recruiting
Study contacts
- Study coordinator: Magnus JC Sjögren, MD, PhD
- Email: jan.magnus.sjoegren@regionh.dk
- Phone: +4538645157
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Eating Disorder Dynamic Intervention
A digital program is tested to help adults with eating disorders by sending real-time, personalized coping tips based on smartphone surveys and sensor data.
-
An AI chatbot to help teens and young adults with eating disorders manage anxiety about weight gain
This project will test an AI-powered chatbot that delivers exposure-based exercises to help adolescents and young adults in a partial hospitalization program reduce anxiety about weight gain.
-
Long-term observation of severe eating disorders
This study is tracking adolescents and adults with severe eating disorders over many years to see what factors affect their health and recovery.
-
Genetic study on eating disorders
This study is trying to understand the genetic and environmental causes of eating disorders by gathering information from 20,000 people with different eating disorders and healthy individuals.
-
New treatment program for adolescents with eating disorders
This study is testing a new treatment program for teenagers with serious eating disorders to see if it helps them feel better and recover over about 16 to 20 weeks.
-
Cognitive evaluation for people with eating disorders
This project tests whether thinking skills (like cognitive flexibility and inhibitory control) and automatic food-related attitudes differ among people aged 14–65 with ARFID, anorexia, or bulimia.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.