- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04343495
UV and Bluelight Dosimetry
Pilot Studies of UV-A, UV-B, and Blue-light Dosimetry Sensors
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age ≥18 years old
- Subjects willing and able to comply with requirements of the protocol
- Subjects speaking English
Exclusion Criteria:
- Age <18 years old
- Subjects unwilling and unable to comply with requirements of the protocol
- History of skin allergy to medical adhesive tape or rubber bands/elastic
- Lack of proficiency in English
- Skin disorders affecting skin integrity
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of various types of light exposure at various, targeted regions of the body while engaging in a different activities and settings.
Time Frame: Time Frame: 1 year
|
After sensors are removed researchers will collect dosimetry data using a phone application using Near Field Communication (NFC) with a phone that is restricted to research use only in this study. Location, indoor/outdoor conditions and time that the devices are used will be recorded by the study team. Location, external environmental factors (weather, UV index) and activities will be recorded by the research administrators. |
Time Frame: 1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- STU00209872
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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