PROspective Longitudinal All-comer Inclusion Study in Eating Disorders
Recruiting
Observational Study
Anorexia Nervosa
Bulimia Nervosa
Binge-Eating Disorder
Eating Disorder NOS
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,000 (estimated)
- Sponsor
- Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg Hospital · Other
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About This Trial
The PROLED study is a prospective and longitudinal study of patients with Eating Disorders. Annual interviews and collection of biological samples are done, as well as during changes in disease course e.g. during hospitalization. Included are qualitative interviews, psychometric tests, questionnaires which are used to collect data on psychopathology. There is also collection of blood, urine and fa…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Eating Disorder (ICD-10)
Exclusion Criteria:
* Forced care/non-voluntary
Contacts