- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04934631
Testing the Utility of a Competence Scale for CBT-ED Therapists
Testing the Utility of a Clinician Competence Scale for Therapists Using Evidence-based Cognitive Behavioural Therapy With Eating Disorder Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Cognitive-behavioural therapy for eating disorders (CBT-ED) is currently one of the NICE (2017) recommended treatments for anorexia nervosa and the only treatment recommended for bulimia nervosa, binge-eating disorder and other specified feeing and eating disorders. When clinicians adhere to evidence-based CBT-ED treatment manuals, CBT-ED has shown demonstrable levels of effectiveness in a range of eating disorders, comparable to outcomes in controlled research settings. A key component of CBT-ED found so effective in the treatment of eating disorders is a stronger focus on behavioural change tasks which is key for changing biased thinking. However, clinicians often drift from using behavioural change components and instead focus more on the cognitive aspects of therapy, or indeed drift away from treatment manuals substantially. Therefore, a suitable measure that can accurately assess how well a clinician is delivering the therapeutic competences that ensures patients are receiving evidence-based CBT-ED thus providing them with the best chance of reaching maximum recovery is important. Whilst numerous scales have been developed, none have yet been found suitable for eating disorders, as they do not have a strong focus on the key behavioural aspects of CBT-ED. Therefore, a team of clinical researchers developed the Cognitive Behaviour Therapy Scale for Eating Disorders (CBTS-ED). This pilot study will use CBT-ED therapy session audio-recordings, and different expert and non-expert raters to a) assess the inter-rater reliability of the CBTS-ED and b) assess whether the CBTS-ED can accurately detect improvement in competence among clinicians currently undergoing post-graduate diploma training in CBT-ED. The findings from this study will provide information about the reliability of the CBTS-ED scale and its possible future uses in predicting patient outcomes.
National Institute for Health and Care Excellence (2017). Eating disorders: recognition and treatment (NICE guideline NG69). Available at: https://www.nice.org.uk/guidance/ng69
Study Type
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Therapist Inclusion Criteria:
- Qualified clinicians with a core National Health Service (NHS) profession currently undergoing post-graduate diploma training in CBT-ED at either the University of Sheffield or University College London (UCL), or;
- Qualified clinicians not on the CBT-ED training course but delivering CBT-ED
- Treating adult (18+ years) eating disorder patients
- Have a good understanding of written and verbal English
Patient Inclusion Criteria:
- Primary diagnosis of an eating disorder
- Accessing CBT-ED
- Aged 18+ years
- Have a good understanding of written and verbal English
- Have the capacity to provide written informed consent
Rater Inclusion Criteria:
- Specialists in the field of CBT-ED, or;
- Qualified clinicians who do not ordinarily work with eating disorder patients, or;
- CBT-ED trainees at Sheffield University or UCL, or;
- CBT-ED training course supervisors at Sheffield University or UCL
- Have a good understanding of written and verbal English
Therapist Exclusion Criteria:
- Non-qualified clinicians
- Non CBT-ED clinicians
- Clinicians only treating children or young people with eating disorders (aged 17 years or younger)
- Have little understanding of written and verbal English
Patient Exclusion Criteria:
- Non-eating disorder patients
- Eating disorder patients who are accessing treatment other than CBT
- Aged 17 years or younger
- Have little understanding of written and verbal English
- Lack the capacity to understand the project and provide written informed consent
Rater Exclusion Criteria:
- Little understanding of written and verbal English
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
CBT-ED trainees and therapists.
Qualified clinicians delivering CBT-ED throughout a variety of treatment settings, working with adult eating disorder patients.
Clinicians will audio-record CBT-ED therapy sessions with their eating disorder patients.
|
Therapists will deliver treatment as usual (CBT-ED) to eating disorder patients.
Therapy session will be audio recorded.
|
Eating Disorder patients.
Adult (18+ years) eating disorder patients currently accessing CBT-ED from one of the CBT-ED therapists/trainees stated above.
Patients will have one of their therapy sessions audio-recorded.
|
Therapists will deliver treatment as usual (CBT-ED) to eating disorder patients.
Therapy session will be audio recorded.
|
Raters/Judges.
Either experts or non-experts in the field of CBT-ED.
Raters will use the CBTS-ED to assess clinician competence when listening to the therapy session audio-recordings.
|
Independent raters will assess CBT-ED competence using the Cognitive-Behavioural Therapy Scale for Eating Disorders (CBTS-ED).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reliability of the CBTS-ED
Time Frame: 12 months
|
Internal reliability of the CBTS-ED (Cronbach's Alpha) and the inter-rater reliability of the CBTS-ED (weighted Kappa statistic).
|
12 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Glenn Waller, University of Sheffield
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 298732
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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