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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02700620
Other study ID # 2014-426-31
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2015
Est. completion date December 2017

Study information

Verified date December 2023
Source Linkoeping University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

As above


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date December 2017
Est. primary completion date June 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Have reoccurring eating disorder uns or bulimia - BMI above 17,5 Exclusion Criteria: - Suicide prone - Ongoing psychological treatment

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Internet-delivered CBT
Guided internet treatment

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Linkoeping University

Outcome

Type Measure Description Time frame Safety issue
Primary Eating Disorders Examination Questionnaire post (8 weeks)
Secondary Quality of Life Inventory (QOLI) Pre and post (8 weeks)
Secondary Body Shape Questionnaire (BSQ) post (8 weeks)
Secondary Patient Health Questionnaire (PHQ-9) post (8 weeks)
Secondary Generalised Axiety Disorder Assessment (GAD-7) post (8 weeks)
Secondary Satisfaction With Life Scales (SWLS) post (8 weeks)
Secondary Expectancy/Credibility Questionnaire (CEQ) post (8 weeks)
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