UV Dosimetry Feedback in NMSC Patients
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|ClinicalTrials.gov Identifier: NCT03757663|
Recruitment Status : Recruiting
First Posted : November 29, 2018
Last Update Posted : December 5, 2018
|Condition or disease||Intervention/treatment||Phase|
|Non-Melanoma Skin Cancer||Behavioral: UV Counseling||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||120 participants|
|Intervention Model:||Single Group Assignment|
|Intervention Model Description:||Each participant will self-report skin protective behaviors and attitudes before wearing a UV dosimeter for 3 weeks. After the wear period, the study team provides feedback based on UV exposure. The participant will then wear the device again for 3 weeks.|
|Masking:||None (Open Label)|
|Official Title:||UV Dosimetry Feedback in Non-Melanoma Skin Cancer Patients|
|Actual Study Start Date :||March 12, 2018|
|Estimated Primary Completion Date :||December 2022|
|Estimated Study Completion Date :||December 2023|
Experimental: UV Dosimeter
UV Dosimeter will measure participants' UV exposure for two separate 3-week periods.
Behavioral: UV Counseling
Participants will self-report their knowledge and attitudes related to UV exposure. They will then wear a dosimeter for 3 weeks. After, the study team will counsel the participants on their UV levels and exposure, creating a personal plan and advice for avoiding sun exposure before letting the participants wear the dosimeter for an additional 3 weeks.
- Identify Discrepancies of Self-Reported Sun Exposure and Actual Sun Exposure [ Time Frame: Start of study to end of study, up to 3 months ]Measured using individual dosimeters and comparing it to what participants state they believe their level of sun exposure is
- Identify Discrepancies of Self-Reported Sun Exposure and Actual Sun Exposure [ Time Frame: Start of study to end of study, up to 3 months ]Compare specific sun exposure behaviors responsible for the level of exposure versus what could be done to lessen it
- Behavioral Intervention and immediate follow-up [ Time Frame: Start of study to end of study, up to 3 months ]Participants will receive a personalized feedback plan and the success of the plan will be measured through individual dosimetry. We will track real time change in sun exposure based on repeat UV dosimetry.
- Long Term Follow Up - longitudinal change in sun exposure based on dosimetry [ Time Frame: Start of study to end of study, up to 3 months ]Track the longitudinal change in sun exposure comparing baseline UV dosimetry measurements to 3 month follow up dosimetry measurements to determine if the changes observed in outcome 3 are maintained.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03757663
|Contact: Sarah Robertsemail@example.com|
|United States, Colorado|
|University of Colorado||Recruiting|
|Aurora, Colorado, United States, 80045|
|Contact: Sarah Roberts 303-724-3912 firstname.lastname@example.org|
|Principal Investigator: Myles Cockburn, PhD|
|Principal Investigator:||Myles Cockburn, PhD||University of Colorado, Denver|