跳至主要内容
临床试验/NCT04800757
NCT04800757已完成不适用

VALES+Tú: Targeting Psychosocial Stressors to Reduce Latino Day Laborers Injury Disparities

The University of Texas Health Science Center, Houston1 个研究点 分布在 1 个国家目标入组 325 人开始时间: 2021年5月11日最近更新:
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
325
试验地点
1
主要终点
Change in Work Hazard Exposure as Assessed by a Survey

研究概览

简要总结

The purpose of this study is to determine the efficacy of VALES+Tú in reducing hazardous exposures at work and to determine the mediating effect of psychosocial stressors on VALES+Tú primary outcomes

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

入选标准

  • •self-identify as Hispanic or Latino
  • •be present at the corner for the purpose of looking for work

排除标准

  • •have not been previously hired to work at a corner
  • •symptoms of COVID-19 in the previous 48 hours

研究组 & 干预措施

individual (Brief Motivational Intervention)

Experimental

干预措施: individual -Brief Motivational Intervention (BMI) (Behavioral)

Group (Group Problem Solving)

Experimental

干预措施: Group (Group Problem Solving) (Behavioral)

Standard of Care

Placebo Comparator

干预措施: Standard of Care (OSHA 10 Safety Cards) (Behavioral)

结局指标

主要结局

Change in Work Hazard Exposure as Assessed by a Survey

时间窗: Baseline, 4 weeks post intervention

Total score on the work hazard exposure survey ranges from 1 - 4, with a higher score indicating greater work hazard exposures. The data are reported as score at post-intervention minus score at baseline.

Change in Work Conditions as Assessed by a Survey

时间窗: Baseline, 4 weeks post intervention

Total score on the work conditions survey ranges from 1 - 4, with a higher score indicating greater adverse work conditions. The data are reported as score at post-intervention minus score at baseline.

次要结局

  • Number of Participants That Implemented the Safety Plan as Assessed by a Survey(4 weeks post intervention)
  • Change in Safety Practices as Assessed by a Survey(Baseline, 4 weeks post intervention)

研究者

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

Maria Eugenia Fernandez-Esquer

Associate Professor

The University of Texas Health Science Center, Houston

研究点 (1)

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