Validation of SHADE a Mobile Technology for Monitoring of Ultraviolet Exposure
Completed · Not applicable
Conditions studied: Skin Cancer, Actinic Keratoses, Ultraviolet-Induced Change in Normal Skin, Behavior, Health, Behavior, Risk Reduction
In brief
This study will evaluate the safety and effectiveness of Shade for the management of UV-induced skin complications and data collected from this study will be used to support the proposed indications for use.
Key facts
- Study ID
- NCT03315286
- Run by
- Weill Medical College of Cornell University
- People needed
- 111
- Starts
- 2017-10-11
- Expected to finish
- 2019-03-31
- Last updated by the study team
- 2019-12-18
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- between 18-80 years of age
- given a diagnosis of actinic keratosis in the past year and/or has had a history of >5 actinic keratosis over the past 5 years
- has a compatible smartphone ((Apple version >= 7, Android version >= 4.4.2; no Jitterbug or Samsung Galaxy J3)
- willing to commit to dermatology visits (including standard of care visits) every 3 months for 6 months
You may not qualify if…
- received UV therapy within the past 6 months
- work/lifestyle incompatible with wearing a UV sensor over the course of 1 year
- has difficulty controlling UV exposure
- has a medical condition judged incompatible with the study by the enrolling physician including the presence of an ICD or an existing plan for extended inpatient treatment
- has received field therapy (i.e., entire face or scalp) for the treatment of actinic keratosis (i.e., topical imiquimod, 5-fluorouracil, photodynamic therapy) in the past 3 months
- is an employee or direct relative of an employee of the investigational site or study sponsor
Where it is running
- Weill Medical College of Cornell University — New York, New York, United States
Full record on ClinicalTrials.gov
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