Using an Evidence-based Lay Health Worker Program to Increase Breast and Cervical Cancer Screening in Low-Income Hispanic Women in Houston
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,025
- 试验地点
- 2
- 主要终点
- The primary outcome for breast cancer screening outcome based on mammography screening behavior measured among participants using self-report.
研究概览
简要总结
The primary purpose of this study is adapt the Cultivando la Salud (CLS) intervention for a new community and priority population and to train community health workers (promotoras) from the Prosalud promotora program to implement the adapted CLS breast and cervical cancer screening program. The adaptation and delivery of the CLS intervention program focuses on meeting the needs and supporting of CHWs and Hispanic/Latina women in the Greater Houston Area. Finally, this study aims to evaluate the process and effect of the adapted CLS program (renamed Salud en Mis Manos (SEMM) on increasing mammography and cervical cancer screening.
详细描述
CHWs identify women in the community in need of breast and/or cervical cancer screening. Based on their screening needs, they invite women to participate in the CLS behavioral intervention. Women are randomized to intervention and usual care comparison (delayed intervention) groups. After women are consented to participate in the study, the study team administers the baseline survey. After the baseline survey is administered, the CLS-adapted intervention (renamed Salud en Mis Manos), is delivered to participants randomized to the intervention group. After the follow-up survey is administered to the participants, women in the comparison group are offered the CLS (SEMM) intervention.
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
- None
入排标准
- 年龄范围
- 21 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •women who identify as Hispanic/Latina ancestry or descent and live in the Greater Houston Area in Texas
- •no previous diagnosis of breast or cervical cancer
排除标准
- •Pregnant women, and women who are adherent to screening guidelines
- •prior or current cancer diagnosis
结局指标
主要结局
The primary outcome for breast cancer screening outcome based on mammography screening behavior measured among participants using self-report.
时间窗: end of evaluation period (6 month follow-up survey, through completion of hard to follow-up period on average 10 months).
Outcomes based on self-report on follow-up survey
The primary outcome for cervical cancer screening outcome based on Pap screening behavior measured among participants using self-report.
时间窗: end of evaluation period (6 month follow-up survey, through completion of hard to follow-up period on average 10 months).
Outcomes based on self-report on follow-up survey
次要结局
未报告次要终点
研究者
Lara Savas
Assistant Professor
The University of Texas Health Science Center, Houston