Not provided
Not provided
Not provided
Not provided
Not provided
Study closed
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This study aims to characterize UV exposures among NMSC patients (those with a history of skin cancer) and to pilot an innovative behavioral intervention to decrease modifiable UV exposures. It will use UV dosimeters to objectively measure UV exposure and provide time and activity specific UV data on an individual level. These data will be used to develop a targeted and personalized behavioral feedback plan with counseling aimed at effective sun exposure behavior change
The study will focus on helping to prevent NMSC and its associated morbidity through learning when patients are unintentionally exposed to extreme UV radiation. It will then help to create manageable and realistic behavioral interventions to reduce exposure, while also educating patients of the dangers of abundant sun exposure.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| UV Dosimeter | Experimental | UV Dosimeter will measure participants' UV exposure for two separate 3-week periods. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| UV Counseling | Behavioral | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Identify Discrepancies of Self-Reported Sun Exposure and Actual Sun Exposure | Measured using individual dosimeters and comparing it to what participants state they believe their level of sun exposure is | Start of study to end of study, up to 3 months |
| Identify Discrepancies of Self-Reported Sun Exposure and Actual Sun Exposure | Compare specific sun exposure behaviors responsible for the level of exposure versus what could be done to lessen it | Start of study to end of study, up to 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Behavioral Intervention and immediate follow-up | 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. | Start of study to end of study, up to 3 months |
| Long Term Follow Up - longitudinal change in sun exposure based on dosimetry |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Myles Cockburn, PhD | University of Colorado, Denver | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Colorado | Aurora | Colorado | 80045 | United States |
Not provided
| ID | Term |
|---|---|
| D001519 | Behavior |
| D000068356 | Self-Control |
| ID | Term |
|---|---|
| D012919 | Social Behavior |
Not provided
Not provided
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.
Not provided
Not provided
Not provided
Not provided
|
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. |
| Start of study to end of study, up to 3 months |