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临床试验/NCT05649072
NCT05649072招募中不适用

Identifying Underserved Individuals inTexas With Hereditary Cancer Risk Using Mobile Mammography Units and Telegenetics.

M.D. Anderson Cancer Center2 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2022年11月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
1,000
试验地点
2
主要终点
To identify underserved women at risk for hereditary breast and colorectal cancers eligible for standard-of-care genetic counseling using national screening guidelines.

研究概览

简要总结

Identifying women at risk for hereditary cancer potentiates prevention, early detection or personalised treatment against cancer. We using mobile mammography units will provide genetic sceening and testing services to underserved women coming for thier mammograms to these units.

详细描述

Objectives:

  1. To identify underserved women at risk for hereditary breast and colorectal cancers and would be eligible for standard of care genetic counseling and testing using national screening guidelines.
  2. To provide education to providers and patients regarding hereditary cancers using previously IRB approved educational material and short video.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Any woman scheduled at Project VALET mammography screening mobile units will be eligible for this study.

排除标准

  • 未提供

研究组 & 干预措施

Genetic Testing and Counseling

Other

Participants will be given a saliva collection kit to collect a saliva sample for hereditary cancer and genetic testing. The kit includes all standard paperwork and instructions for collecting the sample and shipping the kit back to the genetic testing company (Invitae).

干预措施: Genetic Testing and Counseling (Behavioral)

Screening Form

Other

Participants will complete a screening form to assess your risk of hereditary breast and colorectal cancers.

干预措施: Screening Form (Behavioral)

结局指标

主要结局

To identify underserved women at risk for hereditary breast and colorectal cancers eligible for standard-of-care genetic counseling using national screening guidelines.

时间窗: through study completion; an average of 1 year.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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