- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01850433
Internet Cognitive Behavior Therapy (CBT) for Body Dysmorphic Disorder (BDD)
August 15, 2017 updated by: Christian Rück, Karolinska Institutet
Internet-based Cognitive Behavior Therapy for Body Dysmorphic Disorder: A Pilot Study
The primary aim is to develop, and test the feasibility, of a novel and protocol-based cognitive behaviour therapy (CBT) treatment for body dysmorphic disorder (BDD) administered via the Internet.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
23
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Stockholm, Sweden, 141 86
- M46 Huddinge sjukhus, Internetpsykiatrienheten/mottagningen för tvångssyndrom
-
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- outpatients
male or female
-≥ 18 years
- currently living in Stockholm county
- primary diagnosis of BDD according to the DSM-IV-TR
- signed informed consent
- regular access to a computer with Internet access and skills to use the web.
Exclusion Criteria:
- psychotropic medication changes within two months prior to the treatment
- completed CBT for BDD within the last 12 months
- BDD-YBOCS < 12 at psychiatrist visit
- other primary axis I diagnosis
- current substance dependence
- lifetime bipolar disorder or psychosis
- suicidal ideation
- Axis II diagnosis that could jeopardize treatment participation
- other current psychological treatment that could affect BDD symptoms
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Internet CBT
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Body dysmorphic disorder symptoms
Time Frame: Measured after 12 weeks of treatment, and after 3 months after treatment
|
Measured after 12 weeks of treatment, and after 3 months after treatment
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Functioning and life satisfaction
Time Frame: After 12 weeks of treatment, and 3 months after treatment
|
After 12 weeks of treatment, and 3 months after treatment
|
Depressive symptoms
Time Frame: After 12 weeks of treatment, and 3 months after treatment
|
After 12 weeks of treatment, and 3 months after treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2013
Primary Completion (Actual)
March 1, 2014
Study Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
May 7, 2013
First Submitted That Met QC Criteria
May 8, 2013
First Posted (Estimate)
May 9, 2013
Study Record Updates
Last Update Posted (Actual)
August 18, 2017
Last Update Submitted That Met QC Criteria
August 15, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BDD-P
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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