跳至主要内容
临床试验/NCT07218848
NCT07218848进行中(未招募)不适用

ProSalud: A Health Promotion Project to Reduce Cancer Risk in Latinos Living in Rural/Agricultural Communities Within Moffitt's Catchment Area

H. Lee Moffitt Cancer Center and Research Institute4 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2025年5月22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
52
试验地点
4
主要终点
Acceptability

研究概览

简要总结

The purpose of the study is to find out if Latino families living in rural parts of Florida are interested in learning about cancer prevention through our ProSalud program and whether it helps them make healthier choices to lower their risk of cancer. The study will also gather people's opinions about the program to find ways to improve it in the future. For the first part of our study, Latino parents with children between the ages of 6 and 12 will be invited to take part in a one-hour (or one-and-a-half-hour) workshop. The workshop will teach about healthy habits like eating well, being active, and protecting skin from the sun. For the second part of the study, some parents who participated in the workshops will be randomly chosen to join a focus group. In the focus group, they'll be asked questions to help us make the workshop better and make sure it fits the culture, needs, and preferences of Latino families in rural communities.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

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

  • Inclusion and

排除标准

  • We will include adults of any age and sex who are parents of a 6- to 12-year-old child. Parents must speak Spanish and be able to read and write at the 4th-grade level. Parents who speak English in addition to Spanish can also take part in the study, always considering that the workshop will be conducted in Spanish.
  • Individuals who are wards of the state will be excluded from participation in this study.
  • If a participant chooses not to take part at any point, they may do so without any consequences or loss of services provided through RCMA. This ensures that their rights are protected, and their decision will not affect their access to any services or support.
  • We may, by chance, include students and employees. However, we do not plan on collecting information that would indicate any of these statuses. No wards will be included in the study. Wards will not be included as research participants. Because recruitment will happen through RCMA, we anticipate most participants to be socially and/or economically disadvantaged. Participation in this study is entirely voluntary.

研究组 & 干预措施

ProSalud

Experimental

Aim 1: Quantitatively assess feasibility and acceptability of ProSalud and explore changes in cancer risk reduction behaviors.

Aim 2: Qualitatively examine ways to optimize ProSalud. After Aim 1 follow-up is completed, we will recruit a subgroup of parent participants and conduct focus groups to further assess ProSalud with the goal of refining and optimizing our culturally tailored health promotion and cancer prevention workshop to best meet needs and preferences of Latino community members. Semi-structured focus group questions will derive from our quantitative findings in Aim 1.

干预措施: Aim 1 Workshops (Other)

ProSalud

Experimental

Aim 1: Quantitatively assess feasibility and acceptability of ProSalud and explore changes in cancer risk reduction behaviors.

Aim 2: Qualitatively examine ways to optimize ProSalud. After Aim 1 follow-up is completed, we will recruit a subgroup of parent participants and conduct focus groups to further assess ProSalud with the goal of refining and optimizing our culturally tailored health promotion and cancer prevention workshop to best meet needs and preferences of Latino community members. Semi-structured focus group questions will derive from our quantitative findings in Aim 1.

干预措施: Aim 2 Focus Groups (Other)

结局指标

主要结局

Acceptability

时间窗: 1 year

Acceptability will be confirmed if ≥80% of enrolled participants indicate an intention to implement behavioral recommendations.

Demand feasibility and adherence

时间窗: 1 year

The study will be considered feasible if ≥75% of eligible parents approached to participate in the study agree to enroll.

Implementation feasibility

时间窗: 1 year

Implementation feasibility will be established if 100% of data collection is completed in the 1-year timeframe.

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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