- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02700620
Individually Tailored Web-based Cbt for Eating Disorders and the Role of Knowledge Acquisition
Background: Previous studies on Internet-based treatment with eating disorders have shown promising results.
Objective: The first aim of this study was to investigate the effects of a tailored therapist guided internet-based treatment for individuals with eating disorders. The second aim was to examine the role of knowledge acquisition.
Method: 138 participants were recruited. Screening consisted of online questionnaires followed by a telephone interview. A total of 92 participants were included after a semi-structured diagnostic interview and randomized to an 8 week treatment program (n=46) or to a control condition (n=46). Treatment consisted of individually prescribed cognitive behaviour therapy text modules in conjunction with online therapist guidance. The control group consisted of a waitlist who later received treatment.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Have reoccurring eating disorder uns or bulimia
- BMI above 17,5
Exclusion Criteria:
- Suicide prone
- Ongoing psychological treatment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Treatment group
Internet-delivered CBT
|
Guided internet treatment
|
No Intervention: Control group
Waitlist control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Eating Disorders Examination Questionnaire
Time Frame: post (8 weeks)
|
post (8 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Quality of Life Inventory (QOLI)
Time Frame: Pre and post (8 weeks)
|
Pre and post (8 weeks)
|
Body Shape Questionnaire (BSQ)
Time Frame: post (8 weeks)
|
post (8 weeks)
|
Patient Health Questionnaire (PHQ-9)
Time Frame: post (8 weeks)
|
post (8 weeks)
|
Generalised Axiety Disorder Assessment (GAD-7)
Time Frame: post (8 weeks)
|
post (8 weeks)
|
Satisfaction With Life Scales (SWLS)
Time Frame: post (8 weeks)
|
post (8 weeks)
|
Expectancy/Credibility Questionnaire (CEQ)
Time Frame: post (8 weeks)
|
post (8 weeks)
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014-426-31
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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