Comparison of Video-Based Versus Written Patient Education on Atopic Dermatitis
NCT ID: NCT00826592
Last Updated: 2015-04-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
80 participants
INTERVENTIONAL
2009-01-31
2009-08-31
Brief Summary
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Detailed Description
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Subjects randomized to the video-based education arm will be instructed to watch a video on the classifications, aggravating factors, and treatment of atopic dermatitis. Subjects randomized to the written education arm will receive written information on the classifications, aggravating factors, and treatment of atopic dermatitis. The contents of the video and the written educational materials will be comparable.
At the end of the study period, 3 months later, subjects will be interviewed regarding their comprehension and attitude towards video-based and written education materials. Additionally, we will use the Patient-oriented Eczema Measure (POEM) questionnaire to assess the difference in subjects' disease severity between the 2 arms.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SINGLE
Study Groups
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Video-based education arm
Subjects receiving the video-based educational material
Patient Educational Materials
In the experimental arm, the intervention is the video-based patient educational material on atopic dermatitis. In the active comparison arm (control arm), the comparison intervention is written patient educational material on atopic dermatitis.
Written education arm:
Subjects receiving the written educational material
Patient Educational Materials
In the experimental arm, the intervention is the video-based patient educational material on atopic dermatitis. In the active comparison arm (control arm), the comparison intervention is written patient educational material on atopic dermatitis.
Interventions
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Patient Educational Materials
In the experimental arm, the intervention is the video-based patient educational material on atopic dermatitis. In the active comparison arm (control arm), the comparison intervention is written patient educational material on atopic dermatitis.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Able to adhere to the study visit schedule and other protocol requirements.
* Capable of giving informed consent.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of California, Davis
OTHER
Responsible Party
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Principal Investigators
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April Armstrong, MD
Role: PRINCIPAL_INVESTIGATOR
University of California, Davis
Locations
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University of California Davis Department of Dermatology
Sacramento, California, United States
Countries
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Related Links
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University of California-Davis Department of Dermatology Clinical Research
Other Identifiers
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200816693-1
Identifier Type: -
Identifier Source: org_study_id
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