Comparison Between Asynchronous Online Care Model With Usual In Office Care for the Management of Atopic Dermatitis

Not Applicable

Completed

• Conditions: Atopic Dermatitis
• Interventions: Other: Conventional in Office Care; Other: Online Teledermatology Care

• Registration Number: NCT00985894
• Lead Sponsor: University of California, Davis

Brief Summary

The purpose of this study is to determine if an asynchronous online model of teledermatology can achieve similar clinical outcomes as compared to conventional in-office care for the management of atopic dermatitis. The investigators also aim to determine the effects of this online care model on patient quality of life as well as patient and physician satisfaction.

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-09
• Study First Submitted: 2009-09-25
• Study First Submitted QC: 2009-09-28
• Study First Posted: 2009-09-29
• Primary Completion: 2012-03
• Study Completion: 2012-03
• Status Verified: 2017-05
• Last Update Submitted: 2017-05-24
• Last Update Posted: 2017-05-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 183

Inclusion Criteria

• Patients aged 4 years or older at time of consent, may be male or female.
• 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

• Non English speaking patients.
• Patients requiring systemic treatment (e.g., cyclosporine, phototherapy).
• Patients requiring close laboratory monitoring.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Usual Care	Conventional in Office Care	Conventional in-office care
Teledermatology	Online Teledermatology Care	Online Telemedicine Group

Primary Outcome Measures

Name	Time	Method
Eczema Area and Severity Index (EASI)	Every 8 weeks
Patient-oriented Eczema Measure (POEM)	Every 8 weeks

Trial Locations

Locations (1)

UC Davis Department of Dermatology; 🇺🇸 Sacramento, California, United States