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N/A N=164 Randomized Triple-blind Prevention

UV Exposure Assessed With Wearable Sensor and Sun Protection

Sunburn, Erythema · Sun Protection

Enrolled (actual)
164
Serious AEs
0.0%
Results posted
Jul 2023
Primary outcome: Primary: Acceptability of Wearing UV Sensor and Receiving Text Messages — 22; 39.1; 40.1; 40.6 score on a scale — p=<0.01

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Goal attainment (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
Sep 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Acceptability of Wearing UV Sensor and Receiving Text Messages
22; 39.1; 40.1; 40.6 <0.01 sig
SECONDARY
Sun Exposure in Participants With Structured vs Unstructured Goal Setting
399.9; 196.8 <0.001 sig

Summary

The goal is to prevent ultraviolet light (UV) overexposure by providing consumers with relevant, easy-to-access, specifically actionable information. This research proposal will develop a UV protection system consisting of an automated real-time counseling framework and a personal dosimeter that overcomes barriers to consumer adoption. These new, wearable sensors take the form of small (< 1 cm), thin (<0.1 mm), lightweight (<0.1 g), battery-free "stickers" that are fundamentally differentiated from other wearable electronics in their modes of use, cost structures and accuracy.

Eligibility Criteria

Cohort Study 1:

Inclusion Criteria

  • history of Stage 0 to IIB melanoma treated within the last five years, age 18-70 years old
  • have a smartphone
  • familiarity with use of mobile apps
  • have skin type 1-3
  • willing to wear the sensor and able to transmit data which requires Wi-Fi in the home
  • Come to the Chicago campus of the medical school

Exclusion Criteria

-

Cohort Study 2: Young adults with sun sensitive skin

Inclusion Criteria

  • history of sun sensitive skin, skin type 1-3
  • have a smartphone and willing to use the UV guard application on the smartphone
  • reliable wireless internet connection to complete daily surveys
  • willing to wear the sensor for 28 days and transmit data and complete daily surveys
  • willing to receive SMS text messages on their personal phone and potentially sync sensor to personal phone using Bluetooth
  • If weather permits, person will spend at least one hour outdoors each day, with at least 30 minutes of that hour being consecutive between the hours of 8 AM and 5 PM

Exclusion Criteria

  • unable to speak English
  • lacking a secure Internet connection or very little experience with smartphones and mobile applications .
  • unable to walk inside and outside independently
  • unable to be outdoors for at least one hour each day (weather permitting)
  • unable to be outdoors for 30 consecutive minutes a day between 8 AM and 5 PM.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03344796). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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