Eating Disorders in Adolescence Clinical Trials
2 recruiting trials for Eating Disorders in Adolescence. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Eating Disorders in Adolescence clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Servicio Canario de Salud (1), Fundació Sant Joan de Déu (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is Universal primary prevention program based on ICTs (other, 1 trial), followed by ED-MINERVA Program.
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Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
Evaluation of a Digital School-Based Intervention for the Primary Prevention of Eating Disorders in Pre-Adolescents...
Background: Eating Disorders (ED) are mental health conditions, characterized by pathological behaviors toward food intake or a persistent obsession with weight control. EDs have...
Evaluation of a New Treatment Program for Adolescents With Eating Disorders: MINERVA Program
The aim of this study is to investigate the efficacy, efficiency, and patient experience of a new intervention program on adolescents with high-complexity eating disorders (ED). A...
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Frequently Asked Questions
There are currently 2 clinical trials for Eating Disorders in Adolescence, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Eating Disorders in Adolescence, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Eating Disorders in Adolescence, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.