Eating Disorder Prevention

2

Review clinical trials related to Eating Disorder Prevention. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Adolescent Chatbot

The purpose of this study is to test an eating disorders prevention digital chatbot program in a diverse group of adolescents.

Participants needed: 400
Trial details
Phase: Phase 2Age: 13-17Biological sex: AllType: InterventionalSponsor: Washington University School of MedicineUpdated: Jul 31, 2025Locations: 1
Eligibility criteria

13 - 17 years old [+5]

Below 13 or older than 17 years of age [+6]

Status: Not yet recruiting

Early Detection of Patients with Eating Disorders in General Practice

The goal of this observational study is to assess the efficacy of the Eating Disorder Proxy Screening Tool for General Practitioner (ED-PSTGP) as a tool for the early detection of eating disorders (EDs) in General Practice (GP). The ED-PSTGP is a hetero-evaluative questionnaire that investigates the presence of suspected eating disorder symptoms among the family members of the person completing the questionnaire. The study will involve adult patients over 18 years old enrolled in a general practice and their family members aged 16 years or older. The main questions it aims to answer are: * Can the ED-PSTGP questionnaire effectively identify patients with potential eating disorders through responses from a family member? * How effective is the ED-PSTGP questionnaire in general practice as an early detection tool for eating disorders? Participants will: * Be asked by their General Practitioner (GP) to complete the ED-PSTGP questionnaire. * If a positive result is found, invite the potentially affected family member to complete additional screening questionnaires online. The potentially affected family member will be offered a teleconsultation with specialists and encouraged to contact the nearest reference center for ED treatment to further investigate potential eating disorders.

Participants needed: 1,200
Trial details
Age: 16+Biological sex: AllType: ObservationalSponsor: Donini Lorenzo MUpdated: Sep 19, 2024
Eligibility criteria

Age ≥ 18 years, for patients enrolled by a General Practitioner (GP) to complete... [+2]

Inability to provide informed consent