Actively Recruiting
Undergraduate Skin Cancer Prevention Trial
Led by University of Utah · Updated on 2024-12-13
528
Participants Needed
1
Research Sites
214 weeks
Total Duration
On this page
Sponsors
U
University of Utah
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The proposed study is a Multiphase Optimization Strategy (MOST) that uses factorial experiments to evaluate individual and combined effects of intervention components to improve intervention efficiency. The study team anticipates enrolling a total of 528 undergraduate students (\>18 years) into the trial to identify intervention approaches that eliminate sunburn, and secondarily to motivate sun protection and discourage tanning. The study team will test personalized risk components: 1) UV Photo, 2) Action Plan, and 3) MC1R Testing. A full factorial experiment will be conducted to test which of the proposed components or their combinations eliminate sunburn over one year. The study team will also examine effects of the intervention on secondary outcomes. Study assessments will be completed at 4 time points: baseline, 1-month post-intervention, 4-months post-intervention, and 15-months post-intervention.
CONDITIONS
Official Title
Undergraduate Skin Cancer Prevention Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 18 years old
- Enrolled as an undergraduate student
- Report at least one sunburn in the last year, and/or indoor tanning at least once in the last year, and/or intentional or unintentional outdoor tanning sometimes, often, or always
- Use sunscreen plus other sun protection behaviors infrequently (never, seldom, or sometimes)
You will not qualify if you...
- Do not read or speak English
- Personal history of skin cancer
AI-Screening
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Trial Site Locations
Total: 1 location
1
Huntsman Cancer Institute
Salt Lake City, Utah, United States, 84112
Actively Recruiting
Research Team
B
Ben Weitzman
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
PREVENTION
Number of Arms
8
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