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Completed Not applicable Interventional Accepts healthy volunteers

Methods of Assessing Sweat-Electrolyte Testing (MAST)

ClinicalTrials.gov ID: NCT07490756

Public ClinicalTrials.gov record NCT07490756. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 7, 2026, 10:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

If you agree to be in this study, you will be asked to report to our exercise science research center for two total visits (2 separate trials separated by at least 4 days) and the total time commitment for this study will be approximately 5 hours. Prior to each trial, you will be provided with urine jugs and food/fluid logs to record food and drink intake for 24hr. You will be asked to log food/fluid intake 24hr leading into trials. We ask that you match your diet for both trials, as much as possible. Also, we ask that you match caffeine consumption prior to trials. Lastly, we ask that you refrain from strenuous exercise and alcohol consumption for at least 12hrs leading into trials. Either of these exclude your participation in the study for safety reasons. You will be asked to provide a small urine sample upon arrival to the lab before trials. The purpose of this is to verify hydration prior to exercise in the heat. If you are not hydrated upon arrival, you will be provided and asked to drink 16oz (a bottle) of water prior to the trial. Next, you will be seated, have 2 electrodes placed on your inner forearm and researchers will apply electrical stimulation for about 5min. Typically, people feel slight tingling or nothing at all during this procedure. This is a passive way of making you sweat on your forearm. Sweat will then be collected via a small disc applied to your forearm. Immediately following this, you will have your nude body mass measured and you will be instrumented with a lab-based sweat collection patch (large band-aid on the forearm), a Gatorade sweat collection patch on the opposite forearm, and the Hdrop sweat detection device on your left upper arm. the hDrop device is non-FDA approved device because it does not provide a medical diagnosis, but serves as an education and recovery tool. These devices will all be synced with electronic applications (phone apps) to assure data collection. You will then self-insert a rectal thermistor \~15cm past the anal sphincter to monitor core temperature throughout exercise (for safety purposes). You will also be fitted with a heart rate strap that goes around your chest. You will then be asked to enter the environmental chamber and exercise for 60min. The environmental chamber will maintain a consistent temperature (80 degrees F) and humidity (\~45% relative humidity). You will be monitored for safety throughout exercise and you will be allowed to cycle (stationary bike) or run or walk (treadmill) at your own pace/intensity. Pace and intensity will be recorded during the first trial and matched for the second trial. Because fluid consumption may impair accuracy of sweat collection devices, participants will not be allowed to consume fluids during exercise.

Study identification

NCT ID
NCT07490756
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
20 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 39 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 6, 2025
Primary completion
Jun 19, 2025
Completion
Feb 12, 2026
Last update posted
Mar 23, 2026

2025 – 2026

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
University of Arkansas Exercise Science Research Center Fayetteville Arkansas 72701

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07490756, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 23, 2026 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07490756 live on ClinicalTrials.gov.

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