Evaluation of Clinical Outcomes in an Online Teledermatology Model for the Management of Psoriasis
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Enrollment
- 64
- Locations
- 1
- Primary Endpoint
- Psoriasis Area Severity Index (PASI)
Study Overview
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 psoriasis. 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:
- Compared to in-person visits, the online care model will result in similar clinical improvement in psoriasis disease severity.
- Compared to in-person visits, the online care model will result in similar improvements in quality of life.
- Providers and subjects in the online group will achieve a similar level of overall satisfaction as those in the in-person group.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Health Services Research
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •18 years of age or older at time of consent, may be men or women.
- •Requiring treatment of psoriasis for medically-indicated reasons.
- •Capable of giving informed consent.
- •Able to have their skin imaged by themselves or by family members.
Exclusion Criteria
- •Non-English speaking individuals.
- •Individuals lacking access to a digital camera and computer with internet connection.
Arms & Interventions
Teledermatology
Online Telemedicine Group
Intervention: Online Teledermatology Care (Other)
Usual Care
Conventional in-office care
Intervention: Conventional in Office Care (Other)
Outcomes
Primary Outcomes
Psoriasis Area Severity Index (PASI)
Time Frame: Every 6-8 weeks
Secondary Outcomes
No secondary outcomes reported
