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Tundra lists 3 Eating Disorder NOS clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.
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NCT07896707
ASSESSMENT OF ORAL HEALTH AND ORAL HEALTH-RELATED QUALITY OF LIFE IN PATIENTS AGED 12-18 YEARS WITH EATING DISORDERS
Although numerous instruments are available to assess oral health-related quality of life (OHRQoL) in adults, there is a paucity of studies evaluating the impact of oral health on quality of life in children and adolescents. In Türkiye, no study has been conducted to assess oral health-related quality of life in patients with eating disorders. The aim of this study is to evaluate and compare the oral health status of individuals diagnosed with eating disorders and healthy individuals without an eating disorder diagnosis using various clinical indices, as well as to assess oral health-related quality of life through questionnaires completed by both patients and their parents. At the conclusion of the study, the treatment needs of the patients will be communicated to both the patients and their parents, and the patients will be referred to the departments of pediatric dentistry and other relevant specialties at a university hospital to receive the necessary dental treatments.
Gender: All
Ages: 12 Years - 18 Years
Updated: 2026-10-27
1 state
NCT06978452
Behavioural Development, Long-term Outcomes and Opportunities to Optimize Youth Mental Health Trajectories
Behavioural Development, Long-term Outcomes and Opportunities to Optimize Youth Mental Health (BLOOM) is a project that aims to overcome age and diagnostic boundaries to generate person-specific longitudinal profiles of mental health in youth aged 9 to 25. The overarching objective is to lay the informational foundation to accurately predict both clinical outcomes and opportunities to optimize health trajectories. This project will recruit youth in need without any mental health diagnosis and follow them annually for 5 years. The present study includes assessment of antecedents, opportunities and outcomes that will establish eligibility for preventive interventions
Gender: All
Ages: 9 Years - 25 Years
Updated: 2025-05-18
1 state
NCT03224091
PROspective Longitudinal All-comer Inclusion Study in Eating Disorders
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 faeces.
Gender: All
Ages: 18 Years - 65 Years
Updated: 2022-04-07
1 state