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Clinical Trials/NCT06821113
NCT06821113RecruitingNot Applicable

Vale+ Tu Salud: Corner-Based Randomized Trial to Test a Latino Day Laborer Program Adapted to Prevent COVID 19

The University of Texas Health Science Center, Houston1 site in 1 country150 target enrollmentStarted: July 3, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
150
Locations
1
Primary Endpoint
Change in COVID-19 vaccination status as assessed by a survey

Study Overview

Brief Summary

The purpose of this study is to determine the cultural, socioeconomic, inter/personal and work-related factors that influence COVID 19 mitigation practices including social distancing, hand-washing and Personal protective equipment (PPE) use, to adapt, implement, and test Vale+Tú Salud in a cluster randomized trial to assess the extent to which LDL report increased adherence with COVID 19 mitigation practices 1 month post intervention and to promote Vale+Tú Salud just-in-time results and increase its capacity to rapidly disseminate findings among groups that serve LDL and other Latino immigrants.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Self-identify as Hispanic or Latino
  • •Be present at the corner for the purposes of looking for work

Exclusion Criteria

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

Arms & Interventions

COVID-19 Group Problem Solving and booster call

Experimental

Intervention: COVID-19 Group Problem Solving (Behavioral)

COVID-19 Group Problem Solving and booster call

Experimental

Intervention: Standard of Care (Behavioral)

COVID-19 Group Problem Solving and booster call

Experimental

Intervention: Booster session (Behavioral)

Standard of Care

Active Comparator

Intervention: Standard of Care (Behavioral)

Outcomes

Primary Outcomes

Change in COVID-19 vaccination status as assessed by a survey

Time Frame: Baseline, 4 weeks post intervention

Change in hand washing frequency as assessed by a survey

Time Frame: Baseline, 4 weeks post intervention

Percentage of participants who report contacting the gold card agency

Time Frame: Baseline, 4 weeks post intervention

Percentage of participants who report contacting the agency for assistance to get food

Time Frame: Baseline, 4 weeks post intervention

Percentage of participants who report contacting the agency for assistance for health care resources

Time Frame: Baseline, 4 weeks post intervention

Change in COVID-19 vaccination status as assessed by a survey

Time Frame: Baseline, 4 weeks post intervention

Change in hand washing frequency as assessed by a survey

Time Frame: Baseline, 4 weeks post intervention

Percentage of participants who report contacting the gold card agency

Time Frame: Baseline, 4 weeks post intervention

Percentage of participants who report contacting the agency for assistance to get food

Time Frame: Baseline, 4 weeks post intervention

Percentage of participants who report contacting the agency for assistance for health care resources

Time Frame: Baseline, 4 weeks post intervention

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
The University of Texas Health Science Center, Houston
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Maria Eugenia Fernandez-Esquer

Associate Professor

The University of Texas Health Science Center, Houston

Study Sites (1)

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