Implementing an Intervention to Reduce Heat Stress and Chemical Exposures

April 15, 2026 updated by: San Diego State University

The investigators are studying the dangers that farmworkers face while working in the fields and at home. The investigators goals are:

  1. Measure how much heat and chemicals farmworkers in Imperial County are exposed to.

    The investigators will ask the participants to wear a special belt under their clothes during work to measure heat. The investigators will also put two small temperature monitors in the participant's home for a day. The investigators will collect a urine sample to check hydration, and also measure the participants height, weight, blood pressure, and some blood markers for diseases using a simple finger-prick test.

    To measure chemicals, the investigators will give the participants a wristband to wear for a week and hang another in the participants home. The investigators will also collect dust from each participant's home with a vacuum. Then, the investigators will analyze everything at San Diego State University.

    After collecting samples, a trained community health worker will ask the participants a few questions about their work, lifestyle, health symptoms, and any hazards they face. The investigators will meet the participants twice at their homes to distribute the tools which will later be collected. Once the tools are collected, the investigators will have the chance to follow up with the participants if they have any questions.

  2. Provide help to lower heat and chemical exposure with the help of community health workers.
  3. Measure heat and chemicals again using the same methods to see if the project made a difference.
  4. Talk to participants about what they liked and how the investigators can make future projects better.

Study Overview

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • El Centro, California, United States, 92243
        • Lideres Campesinas Imperial

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Currently living in Imperial County, California, USA
  • Currently work in agriculture
  • Plan on living in Imperial Valley for the next 6 months

Exclusion Criteria:

  • Not currently living in Imperial County, California, USA
  • Not currently working in agriculture
  • Not planning to live in Imperial Valley for the next 6 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: All participants
All participants will receive the intervention
The intervention will consist of implementing existing tools provided by EPA's Design for the Environment program, CalOSHA and NIOSH sector-specific guidance for agricultural workers, the Imperial County Department of Public Health and materials from California Department of Toxics Substances Control. The investigators will utilize and adjust existing educational tools such as the Heat Illness Prevention plan developed by CalOSHA. In addition to the educational materials, the investigators will give each farmworker cooling working gear to be worn during their work-shift with (specialized clothes that has been used in other occupational settings). The investigators will provide all participants with a low-cost fan filter, known as Corsi-Rosenthal box built jointly by the community health/research team to reduce chemicals at home, and a small A/C unit to reduce heat stress.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Individual heat stress
Time Frame: Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Skin temperature in degrees Celsius derived from skin temperature monitor worn against the participant's skin.
Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Participant household temperature
Time Frame: Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Household temperature in degrees Celsius, derived from weather monitor placed in the participant's home.
Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Participant hydration level
Time Frame: Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Specific gravity of participant's urine
Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Concentration of chemicals measured in silicon wristband worn by study participant
Time Frame: Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Participants will be asked to wear a silicon wristbands twice; once at baseline and again after the intervention. The research team will collect the wristbands and transport them to San Diego State University for analysis of different classes of chemicals, including pesticides, organophosphates, pyrethroids, and legacy pollutants. The chemicals adhered to the wristbands will be extracted in ethyl acetate and then passed through a solid-phase extraction. Extracts will be analyzed using a two-dimensional gas chromatography coupled to time-of-flight mass spectrometry at San Diego State University. The final concentration of each chemical will be expressed as nanograms per gram of wristband.
Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Concentration of chemicals measured in silicon wristbands hung in the participant's household.
Time Frame: Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Silicon wristbands will be hung in participants' homes twice; once at baseline and again after the intervention. The research team will collect the wristbands and transport them to San Diego State University for analysis of different classes of chemicals, including pesticides, organophosphates, pyrethroids, and legacy pollutants. The chemicals adhered to the wristbands will be extracted in ethyl acetate and then passed through a solid-phase extraction. Extracts will be analyzed using a two-dimensional gas chromatography coupled to time-of-flight mass spectrometry at San Diego State University. The final concentration of each chemical will be expressed as nanograms per gram of wristband.
Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
Concentration of chemicals measured in participant's household dust collected with a vacuum
Time Frame: Assessment at baseline (pre-intervention) and again immediately (week) after the intervention
The research team will visit the participant's home twice to collect the dust samples of the living area using a vacuum; once at baseline and again after the intervention. After collection, the research team will transport the dust samples to San Diego State University to measure the concentrations of different classes of chemicals, including pesticides, organophosphates, pyrethroids, and legacy pollutants. The chemicals in the dust will be extracted in ethyl acetate and then passed through a solid-phase extraction. Extracts will be analyzed using a two-dimensional gas chromatography coupled to time-of-flight mass spectrometry at San Diego State University. The final concentration of each chemical will be expressed as nanograms per gram of dust.
Assessment at baseline (pre-intervention) and again immediately (week) after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 7, 2024

Primary Completion (Actual)

December 15, 2025

Study Completion (Actual)

December 15, 2025

Study Registration Dates

First Submitted

May 13, 2024

First Submitted That Met QC Criteria

June 3, 2024

First Posted (Actual)

June 5, 2024

Study Record Updates

Last Update Posted (Actual)

April 16, 2026

Last Update Submitted That Met QC Criteria

April 15, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Dehydration

Clinical Trials on Education and resources provided by community health workers

Subscribe