Actively Recruiting

Age: 16Years +
All Genders
NCT06103929

Adult Eating Disorder Assessment Study

Led by University of Leicester · Updated on 2024-02-14

100

Participants Needed

1

Research Sites

171 weeks

Total Duration

On this page

Sponsors

U

University of Leicester

Lead Sponsor

L

Leicestershire Partnership NHS Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

The hypothesis of the study is that low-cost self-completion questionnaires relating to eating disorder symptoms will predict the subsequent results of a detailed, semi-structured interview assessment of eating disorder symptoms that has been calibrated according to expert clinical diagnostic case thresholds. Eating disorders are recognised as a research priority among healthcare professionals, adults with lived experience, and their carers alike. There is a need for measurement methods that can reliably and systematically identify symptoms of common forms of eating disorder, including those fulfilling agreed diagnostic criteria for anorexia nervosa, bulimia nervosa, and binge-eating disorder. Effective diagnostic interview tools can facilitate early detection of eating disorders. To develop rules for determining whether diagnostic criteria for eating disorders are met, a study involving adults referred to specialist eating disorder services is required. In this study, assessments by eating disorder clinicians will be compared with researcher assessments using a semi-structured interview assessment, the Schedules for Clinical Assessment in Neuropsychiatry version 3 section 9 (SCANv3s9). The study population will consist of 100 adult patients referred to specialist eating disorder services, including patients whose referrals are accepted by these services, as well as those who are not. Clinical assessments and structured interview assessment findings will also be compared with those from widely used screening tools for eating disorders, the Eating Disorder Examination Questionnaire short-form and the SCOFF (Sick, Control, One, Fat, Food) questionnaire. The aim of this study is to evaluate the accuracy of the Eating Disorder Examination Questionnaire Short-Form (EDE-QS) and the SCOFF (Sick, Control, One, Fat, Food) questionnaire in adults referred to specialist eating disorder services, in a comparison with the Schedules for Clinical Assessment in Neuropsychiatry subsection on eating disorders and specialist NHS clinician assessments of the probability of eating disorder. This will help develop appropriate and accurate benchmarks for estimating the prevalence of eating disorder symptoms and clinical diagnoses, in adults referred to specialist eating disorder services, as well as the wider population (through combining the findings from this study with those of the community 2023 Adult Psychiatric Morbidity Survey).

CONDITIONS

Official Title

Adult Eating Disorder Assessment Study

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Leicestershire Partnership NHS Trust

Leicester, United Kingdom, LE4 8BL

Actively Recruiting

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Research Team

A

Associate Professor of Psychiatry & Honorary Consultant Psych, MRCPsych,PhD

CONTACT

T

Traolach S. Brugha, FRCPsych,MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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