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临床试验/NCT02895880
NCT02895880已完成不适用

A Risk Assessment Tool to Increase Statin Use Among High Risk Cancer Survivors: Development and Pilot Testing

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2016年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
49
试验地点
1
主要终点
number of patients who initiated statins after the office visit

研究概览

简要总结

The purpose of this study is to collect initial data on what survivors of childhood, adolescent, and young adult cancer think of how information about statins is communicated. Statins are medications that lower cholesterol. The results of this study will be used to improve the communication about statins. This is to aid patients and their providers in making health care decisions together, also known as shared decision making.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

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

入选标准

  • English speaking
  • A personal history of cancer, tumor, or a related illness
  • Followed in the Adult Long Term Follow Up Program
  • Received ≥ 2000 cGy radiation to the heart/chest
  • ≥Ten years post-radiation therapy to the heart/chest
  • Age ≥ 25 years old

排除标准

  • Evidence of active progression of disease or recurrence
  • Neurocognitive deficits that impair ability to give informed consent
  • Current use of a statin
  • Diagnosis of another primary cancer for which the patient is currently undergoing radiation therapy chemotherapy, or bone marrow transplant
  • Diagnosis of CVD with or without current statin use

结局指标

主要结局

number of patients who initiated statins after the office visit

时间窗: 1 year

This data will allow validation of the adapted tool in the cancer survivor population. Acceptability will be estimated using the tool describe which will be transformed to a 0 to 100 scale and summarized separately in the two populations using means and standard deviations.These preliminary statistics in both populations (intervention and usual care) will be utilized to design a future larger scale study powered to detect a difference between the two groups.

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 (1)

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