跳至主要内容
临床试验/NCT00514254
NCT00514254进行中(未招募)不适用

Endometrial Cancer in Black Women

Memorial Sloan Kettering Cancer Center4 个研究点 分布在 1 个国家目标入组 59 人开始时间: 2007年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
59
试验地点
4
主要终点
Number and percentage of cases and controls approached who sign informed consent

研究概览

简要总结

RATIONALE: Learning about the risk factors for endometrial cancer in black women may help the study of endometrial cancer in the future.

PURPOSE: This clinical trial is studying risk factors for endometrial cancer in black women.

详细描述

OBJECTIVES:

  • Establish and evaluate procedures for conducting a hospital-based case-control study of risk factors for endometrial cancer in black women.

OUTLINE: This is a multicenter study.

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

PROJECTED ACCRUAL:

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
21 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •DISEASE CHARACTERISTICS:
  • •Diagnosed with endometrial cancer within the past year
  • •Self-identified as being black, African-American, black Hispanic, African, or Afro-Caribbean
  • •Healthy controls
  • •Self-identified as being black, African-American, black Hispanic, African, or Afro-Caribbean
  • •No history of endometrial or other cancer (except non-melanoma skin cancer)
  • •No prior hysterectomy
  • •PATIENT CHARACTERISTICS:
  • •Speak English
  • •No medical condition that would make it difficult to complete the interview
  • •PRIOR CONCURRENT THERAPY:
  • •See Disease Characteristics

排除标准

  • 未提供

研究组 & 干预措施

case

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

干预措施: questionnaire administration (Other)

case

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

干预措施: study of socioeconomic and demographic variables (Other)

case

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

干预措施: evaluation of cancer risk factors (Procedure)

control

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

干预措施: questionnaire administration (Other)

control

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

干预措施: study of socioeconomic and demographic variables (Other)

control

Participants complete questionnaires about lifestyle factors and their usual diet and measure their waist and hips. Saliva or buccal specimens are collected for future research.

干预措施: evaluation of cancer risk factors (Procedure)

结局指标

主要结局

Number and percentage of cases and controls approached who sign informed consent

时间窗: 2 years

Proportion of questions with missing data

时间窗: 2 years

Interviewer's evaluation of interview quality and respondent cooperation

时间窗: 2 years

Proportion of participants who rate the study positively on each measure in the post-interview assessment and respondents' suggested changes to the study

时间窗: 2 years

Number and percentage of potential cases and controls approached who are found to be eligible for the study and reasons for being ineligible (including language)

时间窗: 2 years

Number and percentage of cases and controls who complete each part of the study (main questionnaire, diet questionnaire, saliva/buccal specimen)

时间窗: 2 years

Number and percentage of cases who are willing to have tumor specimens used for future research

时间窗: 2 years

Characteristics of cases and controls (demographics, main risk factors, and use of health care and screening)

时间窗: 2 years

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 (4)

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