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Laboratory Heat Biomarker and Cooling Interventions

Laboratory Based Identification of Heat Stress Biomarkers and Effective Cooling Interventions

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07617649
Enrollment
30
Registered
2026-06-01
Start date
2026-06-01
Completion date
2028-06-01
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperthermia

Brief summary

Our study has two goals. The first goal is to find a blood test that can detect signs of strain from heat in the body ("a biomarker"). Second, the study team wants to identify types of devices that can help people cool down quickly. By identifying biomarkers for heat strain, scientists can better track and treat the health effects of heat. The study team will identify such biomarkers by simulating, in a laboratory-based environment, the heat and physical work that real-world workers experience. In addition, the study team plans to test two cooling technologies that might keep people cool during physical activity.

Interventions

OTHERHand cooling table

A participant can rest their hand on the cooling table after the one hour exercise session, and this should cool their body quickly. Cold water is pumped throughout the cooling table.

A participant will tie a bandana that has been soaked in cold water onto their forehead. They will wear this bandana during the one hour exercise session.

Sponsors

Stanford University
Lead SponsorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-50 * Able to communicate in English or Spanish * General good health * A lifestyle that includes regular patterns of modest exercise * Body weight over 80 pounds

Exclusion criteria

* Cannot provide informed consent * Known history of cardiac arrhythmias or having a pacemaker * Difficulty swallowing pills * Planned upcoming X-ray tests or MRI * Known history of gastroparesis, diverticulosis or diverticulitis, or inflammatory bowel disease * Previous surgery on stomach or intestines (except for appendix or gallbladder) * Pregnancy * Self-reported cardiac, kidney, or pulmonary disease, or diabetes * Concurrent use of temperature- or inflammation-modulating medications such as steroids or non-steroidal anti-inflammatory drugs (NSAIDs) * Staff under the direct supervision of any project directors or employed in the laboratory of the study investigators

Design outcomes

Primary

MeasureTime frame
Core body temperatureBaseline through end of study (approximately 2 months).

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJulie Parsonnet, MD

Stanford University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026