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临床试验/NCT03757663
NCT03757663撤回不适用

UV Dosimetry Feedback in Non-Melanoma Skin Cancer Patients

University of Colorado, Denver2 个研究点 分布在 1 个国家开始时间: 2018年3月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Identify Discrepancies of Self-Reported Sun Exposure and Actual Sun Exposure

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients between ages 18 and
  • Must be diagnosed with non-melanoma skin cancer.

排除标准

  • Patients, who at the discretion of the clinician, are too ill or sick.
  • Non-English speaking patients.

研究组 & 干预措施

UV Dosimeter

Experimental

UV Dosimeter will measure participants' UV exposure for two separate 3-week periods.

干预措施: UV Counseling (Behavioral)

结局指标

主要结局

Identify Discrepancies of Self-Reported Sun Exposure and Actual Sun Exposure

时间窗: 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

次要结局

  • Behavioral Intervention and immediate follow-up(Start of study to end of study, up to 3 months)
  • Long Term Follow Up - longitudinal change in sun exposure based on dosimetry(Start of study to end of study, up to 3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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