跳至主要内容
临床试验/NCT00581672
NCT00581672已完成不适用

Anxiety in Black Men With Prostate Cancer: Validation of the Memorial Anxiety Scale for Prostate Cancer in an Sample of Black Men

Memorial Sloan Kettering Cancer Center3 个研究点 分布在 1 个国家目标入组 224 人开始时间: 2010年7月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
224
试验地点
3
主要终点
To establish the psychometric properties of the Memorial Anxiety Scale for Prostate Cancer (MAX-PC) in Black men with prostate cancer.

研究概览

简要总结

This study is being done to see if a standard tool used to check anxiety in white men works well for Black men. The tool is used only for men who have prostate cancer. It is meant to see how the cancer affects men. If the investigators have a good tool, it is more likely that the investigators can help those who have high levels of anxiety. This test is known as the Memorial Anxiety Scale for Prostate Cancer (also called the MAX-PC).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • 18 years of age or older
  • Patients who are being monitored by PSA tests, who will have a PSA test done on the day of their current clinic visit or prior to their clinic visit, but prior to being informed of the results
  • Diagnosis of prostate cancer
  • Ethnicity: Black, African-American, or of African descent (and will include those men who identify as Black and Hispanic).
  • Ability to comprehend and complete questionnaires in English

排除标准

  • Major psychopathology or cognitive impairment likely, in the judgment of the research staff, to interfere with the participation or completion of the protocol
  • Other non-Black or non-African-American ethnic groups

结局指标

主要结局

To establish the psychometric properties of the Memorial Anxiety Scale for Prostate Cancer (MAX-PC) in Black men with prostate cancer.

时间窗: within one to three weeks of receiving their PSA scores from their physician

次要结局

  • To explore the prevalence of distress, anxiety, and depression in Black men with prostate cancer.(within one to three weeks of receiving their PSA scores from their physician)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验