UV and Bluelight Dosimetry

September 27, 2022 updated by: Shuai (Steve) Xu, Northwestern University

Pilot Studies of UV-A, UV-B, and Blue-light Dosimetry Sensors

The objective of this study to assess the efficacy of wearable Ultra Violet (UV) and blue-light sensors in measuring exposure to UV radiation and blue light in a variety of environments and activity settings.

Study Overview

Status

Withdrawn

Study Type

Observational

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adults

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

July 1, 2022

Primary Completion (ANTICIPATED)

December 1, 2023

Study Completion (ANTICIPATED)

February 1, 2024

Study Registration Dates

First Submitted

March 30, 2020

First Submitted That Met QC Criteria

April 10, 2020

First Posted (ACTUAL)

April 13, 2020

Study Record Updates

Last Update Posted (ACTUAL)

September 29, 2022

Last Update Submitted That Met QC Criteria

September 27, 2022

Last Verified

September 1, 2022

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

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Environmental Exposure

Clinical Trials on Wearable Ultra Violet (UV) and blue-light sensors

3
Subscribe