Evaluation of Pilot Online Binge Eating Disorder Group (BEG) in Under 18s.

NCT ID: NCT06703502

Last Updated: 2024-11-25

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 2 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-04-26
• Study Completion Date: 2023-09-26

Brief Summary

The National Institute for Clinical Excellence recommends a cognitive behavioural therapy (CBT) group intervention for binge eating disorder in under-18s. However, there is limited current research in this population. The present study sought to evaluate a CBT group intervention for binge eating disorder in under-18s.

Detailed Description

Background and study aims: The National Institute for Clinical Excellence recommends a cognitive behavioural therapy (CBT) group intervention for binge eating disorder in under-18s. However, there is limited current research in this population. The present study sought to evaluate a CBT group intervention for binge eating disorder in under-18s.

Who can participate? Participants were recruited from the Coventry Warwickshire Partnership Trust's Children and Young People Eating Disorders Team (n=2).

What does the study involve: Participating in a group intervention and completing questionnaires (Eating Disorder Examination - Questionnaire (EDE-Q), Revised Children's Anxiety and Depression Scale (RCADS) Child and RCADS Parent) before the group, at the end of the group and a follow-up appointment, as well as a feedback form at the end of the group intervention.

What are the possible benefits and risks of participating:

• Benefits: Working towards recovering from binge eating disorder
• Risks: As with all therapy, there is a risk of distress due to the topics discussed. There is no more risk than any other group online therapy.

Where is the study run from: Online intervention for participants who are eligible and who are under the care of the RISE Eating Disorders Team within Coventry and Warwickshire NHS Partnership Trust.

When is the study starting and how long is it expected to run for: The study commenced on on 23rd May 2023. The group intervention ran from 20th June 2023 to 26th September 2023.

Conditions

Binge Eating Disorder

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: CROSS_SECTIONAL

Eligibility Criteria

Inclusion Criteria

• Diagnosed with Binge Eating Disorder
• Under 18 prior to the group commencing
• Spoke English fluently

Exclusion Criteria

• If they were underweight. This was measured by percentage median body mass index (%mBMI) as recommended by the Medical Emergencies in Eating Disorders guidelines (Royal College of Psychiatrists, 2022) for under 18s. As such, individuals were excluded if %mBMI was less than 95%
• If they had any physical illness serious enough to prevent the participant from engaging fully in the group and completing the in-between session work
• If they were pregnant
• If they had an eating disorder-induced physical health state requiring regular medical intervention by the nursing team
• If they presented a mental health state requiring stabilisation prior to participating in the group intervention according the assessment team
• If they regularly used alcohol and/or drugs
• If they repeatedly self-harmed to the point of requiring additional interventions
• If they had a living situation not conducive to the start of an intervention (ongoing or upcoming changes).

• Minimum Eligible Age: 12 Years
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Birmingham Newman University

UNKNOWN

Sponsor Role: collaborator

Coventry and Warwickshire Partnership NHS Trust

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Wood End Health Centre

Coventry, West Midlands, United Kingdom

Countries

United Kingdom

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Informed Consent Form: Service User

View Document

Document Type: Informed Consent Form: Parent Carer version

View Document

Document Type: Informed Consent Form: 16+ Service User

View Document

Other Identifiers

320293

Identifier Type: -

Identifier Source: org_study_id