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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00826592
Other study ID # 200816693-1
Secondary ID
Status Completed
Phase N/A
First received January 20, 2009
Last updated April 15, 2015
Start date January 2009
Est. completion date August 2009

Study information

Verified date April 2015
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the effect of video-based patient education with written instruction on subjects' knowledge of atopic dermatitis and their disease severity, measured by the Patient-oriented Eczema Measure (POEM), after viewing the educational materials.


Description:

We plan to conduct a randomized, controlled trial comparing the effect of video-based patient education with written instruction on subjects' understanding of atopic dermatitis and their disease severity.

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.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date August 2009
Est. primary completion date August 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older at time of consent, may be men or women.

- Able to adhere to the study visit schedule and other protocol requirements.

- Capable of giving informed consent.

Exclusion Criteria:

- Non-English speaking individuals.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator)


Intervention

Other:
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.

Locations

Country Name City State
United States University of California Davis Department of Dermatology Sacramento California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Subjects' disease severity measured by the patient-oriented eczema measure (POEM). 3 months No
Secondary Subjects'comprehension and attitude towards video-based and written education materials. 3 months No
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