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临床试验/NCT01373320
NCT01373320已完成不适用

Faith Moves Mountains: A CBPR Appalachian Wellness & Cancer Prevention Program

Nancy Schoenberg1 个研究点 分布在 1 个国家目标入组 1,415 人开始时间: 2010年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,415
试验地点
1
主要终点
Proportion of participants reporting the health behavior of interest (depending on which intervention component(s) were selected)

研究概览

简要总结

The study purpose is to evaluate the effectiveness of a set of culturally appropriate, faith-placed lay health advisor interventions aimed at facilitating smoking cessation and increasing cancer screening among Appalachian participants.

详细描述

The developmental phase of this project incorporated community based participatory research (CBPR) principles to identify the needs and preferences of community members with regard to cancer prevention. In the intervention phase, this group-randomized trial administers and evaluates a set of culturally appropriate interventions aimed at facilitating smoking cessation and increasing cancer screening among participants in 6 distressed Appalachian counties. Faith institutions are recruited and randomized to treatment or wait-list control conditions, and participants are recruited and enrolled within those institutions. Participants select one or more targeted health behaviors from a menu including smoking cessation, colorectal cancer screening, cervical cancer screening, and breast cancer screening, and subsequently receive the intervention(s) aimed at their selected health behaviors.

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

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

入选标准

  • For smoking cessation: age 18 or older; current cigarette smoker; able to provide informed consent
  • For cervical cancer screening: female; age 18 or older AND outside of screening guidelines; able to provide informed consent
  • For breast cancer screening: female; age 40 or older AND outside of screening guidelines; able to provide informed consent
  • For colorectal cancer screening: age 40 or older AND outside of screening guidelines; able to provide informed consent

排除标准

  • For smoking cessation: None
  • For cervical cancer screening: History of cervical cancer; history of hysterectomy
  • For breast cancer screening: History of breast cancer
  • For colorectal cancer screening: History of colorectal cancer

结局指标

主要结局

Proportion of participants reporting the health behavior of interest (depending on which intervention component(s) were selected)

时间窗: Assessed approximately 4 months after baseline

For smoking cessation: Self-reported smoking status. For cancer screenings: Self-reported receipt of cervical, breast, and/or colorectal cancer screening. This assessment occurs after the Early Treatment group has completed the intervention.

次要结局

  • Number of visits completed(Approximately 4 months after baseline)
  • Retention (i.e., number of participants who complete all planned assessment timepoints)(Approximately one year after baseline)
  • Change in stage of readiness to change the selected health behavior(s) from baseline(Assessed approximately 4 months after baseline)

研究者

发起方
Nancy Schoenberg
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Nancy Schoenberg

Sponsor/PI

University of Kentucky

研究点 (1)

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