Comparison Between Asynchronous Online Care Model With Usual In Office Care for the Management of Atopic Dermatitis
NCT ID: NCT00985894
Last Updated: 2017-05-30
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
183 participants
INTERVENTIONAL
2009-09-30
2012-03-31
Brief Summary
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The investigators' hypotheses include the following:
1. Compared to in-person visits, the online care model will result in similar clinical improvement in atopic dermatitis disease severity.
2. Compared to in-person visits, the online care model will result in similar improvements in quality of life.
3. Providers and subjects in the online group will achieve a similar level of overall satisfaction as those in the in-person group.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Teledermatology
Online Telemedicine Group
Online Teledermatology Care
Patients randomized to the intervention group will have their scheduled follow-up visits online via store and forward teledermatology.
Usual Care
Conventional in-office care
Conventional in Office Care
Patients randomized to the control group will have their scheduled follow-up visits via conventional in office care.
Interventions
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Online Teledermatology Care
Patients randomized to the intervention group will have their scheduled follow-up visits online via store and forward teledermatology.
Conventional in Office Care
Patients randomized to the control group will have their scheduled follow-up visits via conventional in office care.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Meet the Hanifin diagnostic criteria for atopic dermatitis.
* Capable of giving informed consent (for patients less than 18 years of age, assent will be obtained from the minor and informed consent will be obtained from a legal guardian).
* Able to image their skin or have someone do it for them.
* Able to adhere to the study visit schedule and other protocol requirements.
* Have access to a computer with internet connection, a digital camera, and an e-mail address.
Exclusion Criteria
* Patients requiring systemic treatment (e.g., cyclosporine, phototherapy).
* Patients requiring close laboratory monitoring.
4 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 W Armstrong, MD
Role: PRINCIPAL_INVESTIGATOR
UC Davis Department of Dermatology
Locations
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UC Davis Department of Dermatology
Sacramento, California, United States
Countries
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References
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Armstrong AW, Johnson MA, Lin S, Maverakis E, Fazel N, Liu FT. Patient-centered, direct-access online care for management of atopic dermatitis: a randomized clinical trial. JAMA Dermatol. 2015 Feb;151(2):154-60. doi: 10.1001/jamadermatol.2014.2299.
Other Identifiers
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200917162
Identifier Type: -
Identifier Source: org_study_id
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