Clinical trial Recruiting at 1 site Observational Ages 16 and up

Assessment of eating disorders in adults using questionnaires

Official title: Evaluation of Eating Difficulties Assessment Measures in Clinical Practice and in Epidemiological Surveys

Run by University of Leicester · NCT06103929 · Data updated 2026-11-12

This study is testing if simple questionnaires can help identify eating disorders like anorexia and bulimia in adults as accurately as detailed interviews with specialists.

Quick facts

Study typeObservational
Ages16 Years and up
SexAll
Enrollment100 (estimated)
SponsorUniversity of Leicester
Academic / other
Locations1 site (Leicester)
StatusRecruiting
StartedJanuary 15, 2024
Main results expectedMay 2027
Study endsMay 2027
Registry record updatedFebruary 14, 2024
Trial IDNCT06103929 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 16 years or older who have been referred to specialist eating disorder services.

Probably not a fit

Patients under 16 years old or those with a clinical diagnosis of intellectual disability 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

This observational study aims to evaluate the effectiveness of low-cost self-completion questionnaires in predicting the results of detailed semi-structured interviews for diagnosing eating disorders. It focuses on common forms of eating disorders such as anorexia nervosa, bulimia nervosa, and binge-eating disorder. The study will involve adults referred to specialist eating disorder services, utilizing established diagnostic criteria as a reference standard. The methodology includes calculating sensitivity, specificity, and other statistical measures to assess the reliability of the questionnaires compared to clinician assessments.

Why it matters

Potential benefit: If successful, this study could enhance early detection and diagnosis of eating disorders, leading to timely and effective treatment for patients.

How similar studies have gone: Previous studies have shown promise in using similar assessment tools for diagnosing eating disorders, indicating potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Individuals aged 16 years or older (on the date of referral to specialist eating disorder services)
* Individuals referred to specialist adult eating disorder services during the study period

Exclusion Criteria:

* Patients under 16 years old and having not been referred to specialist eating disorder services.
* Patients with a clinical diagnosis of intellectual disability will be excluded on the basis that the SCAN is not intended for use in this patient group.
* Patients lacking capacity to consent to take part.
* Participants who lose capacity during their participation will be withdrawn from the study (with data collected up until the point of withdrawal being retained).
* Participants who are unable to understand written and verbal English.

Where it's running

  • Leicestershire Partnership NHS Trust
    Leicester, United Kingdom
    Recruiting

Study contacts

  • Principal investigator: Samuel J. Tromans — University of Leicester
  • Study coordinator: Associate Professor of Psychiatry & Honorary Consultant Psych, MRCPsych,PhD
  • Email: st386@leicester.ac.uk
  • Phone: +44 (0)116 252 5451

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.