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临床试验/NCT01910350
NCT01910350已完成不适用

Kin KeeperSM: Reducing Disparities Through Cancer Literacy and Screening

Michigan State University2 个研究点 分布在 1 个国家目标入组 516 人开始时间: 2010年7月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
516
试验地点
2
主要终点
First time AND appropriately timed, clinical breast exam, mammogram, pap test

研究概览

简要总结

  1. To determine if the Kin KeeperSM Cancer Prevention Intervention increases first time and appropriately timed breast cancer screening rates among Black, Latina and Arab women; 2) To determine if the Kin KeeperSM Cancer Prevention Intervention increase first time and appropriately time cervical cancer screening rates among Black, Latina and Arab women; 3) To measure functional cancer literacy over time at the individual and familial level and 4) Assess rates of healthcare utilization cost among women in the Kin KeeperSM intervention and control-comparison groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
21 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Participants:self-identified as Black Latina and Arab women ho can recruit at least two bloodline female family members (mother daughter sister, etc.; can accommodate two in-home visits by a community health worker; and 21-70 years of age.

排除标准

  • are not self-identified as Black, Latina, or Arab; do not have direct bloodline relatives; and are younger than 21 or older than 70 years of age.

研究组 & 干预措施

Cancer prevention intervention

Experimental

Cancer prevention intervention: Experimental group receives intensive 2 hour education in each breast and cervical cancer risks and prevention intervention, and face to face reading of post intervention surveys by an community health worker.

干预措施: Kin KeeperSM Cancer Prevention Intervention (Behavioral)

Control group receives standard care

Active Comparator

The control group receives reading materials and brochures on breast and cervical cancer such as one would receive in a doctors office and post condition surveys. All materials are read by the participant without the interaction or assistance of the community health worker.

干预措施: Standard of care (Other)

结局指标

主要结局

First time AND appropriately timed, clinical breast exam, mammogram, pap test

时间窗: Baseline through 36 months.

Participants will complete measures every 6 months (baseline, 12 mo., 18 mo., 24 mo., 30 mo. \& 36 mo.)to measure increases in screening rates for experimental vs. control group.

次要结局

  • Increased Breast and Cervical Cancer Literacy rates.(Baseline-36 months.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Karen Williams

Professor

Michigan State University

研究点 (2)

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