Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07222995

Hybrid Effectiveness-Implementation Trial to Integrate Precision Skin Cancer Risk Feedback in FQHCs

Led by H. Lee Moffitt Cancer Center and Research Institute · Updated on 2026-02-05

2900

Participants Needed

2

Research Sites

260 weeks

Total Duration

On this page

Sponsors

H

H. Lee Moffitt Cancer Center and Research Institute

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to examine how different messages about risk of skin cancer can impact the uptake of skin cancer prevention activities.

CONDITIONS

Official Title

Hybrid Effectiveness-Implementation Trial to Integrate Precision Skin Cancer Risk Feedback in FQHCs

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a patient of any race or ethnicity attending one of the six Tampa Family Health Centers.
  • Be 18 years of age or older.
  • Self-report skin cancer risk behaviors within the past 12 months, including intentional sun exposure (e.g., outdoor or indoor tanning) or unintentional sun exposure leading to sunburn.
  • Be willing to complete a baseline questionnaire and provide a saliva sample for MC1R genotyping.
  • Be able to provide informed consent (written or electronic).
  • Prefer English or Spanish for communication and study materials.
Not Eligible

You will not qualify if you...

  • Do not report any skin cancer risk behaviors (i.e., no tanning or sunburning in the past 12 months).
  • Are unwilling or unable to complete the baseline assessment or return the saliva kit.
  • Decline to provide informed consent.
  • Are under 18 years of age.

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Trial Site Locations

Total: 2 locations

1

Moffitt Cancer Center

Tampa, Florida, United States, 33612

Actively Recruiting

2

Memorial Sloan Kettering Cancer Center

New York, New York, United States, 10065

Active, Not Recruiting

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Research Team

R

Rania Abdulla

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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