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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04767347
Other study ID # 1902420140
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2021
Est. completion date May 4, 2023

Study information

Verified date November 2023
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

An epidemic of chronic kidney disease is occurring in laborers who undertake physical work outdoors in hot conditions. The reason for this is unknown, but may be related to kidney dysfunction caused by increases in body temperature and dehydration. The current heat stress recommendations for workers were not developed with regards for kidney health. The purpose of this study is to determine if the current recommendations protect against kidney dysfunction.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date May 4, 2023
Est. primary completion date May 4, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 44 Years
Eligibility Inclusion Criteria: - Men and women - 18-44 y old - Body mass index =35.0 kg/m2 - Self-reported to be healthy. Exclusion Criteria: - Not within defined age range - Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2 - Deemed highly active according to the physical activity questionnaire (i.e., >3500 MET*min/wk) - Body mass index >35.0 kg/m2 - Current or history of any renal disease, heart disease, stroke, immune or autoimmune disease, and/or gastrointestinal disease/surgery - Hypertension during screening (systolic blood pressure >139 or diastolic blood pressure >89) - Using medications that blunt the physiological response to exercise (e.g., beta blockers) - Prescription medication with a known side effect of impaired temperature regulation or fluid balance (e.g., diuretics) - Positive pregnancy test at any time during the study or breast feeding - Current tobacco or electronic cigarette use or consistent use within the last 2 years - Inability to safely complete the peak oxygen uptake test

Study Design


Intervention

Other:
23.0°C WBGT - Fixed Work Rate
For four hours, participants will walk on a treadmill to elicit 430 W of metabolic heat production in the following conditions: 23.0°C WBGT (29°C, 46% relative humidity) @ 60 min exercise per hour
25.5°C WBGT - Fixed Work Rate
For four hours, participants will walk on a treadmill to elicit 430 W of metabolic heat production in the following conditions: 25.5°C WBGT (31°C, 52% relative humidity) @ 45 min exercise per hour
27.5°C WBGT - Fixed Work Rate
For four hours, participants will walk on a treadmill to elicit 430 W of metabolic heat production in the following conditions: 27.5°C WBGT (33°C, 53% relative humidity) @ 30 min exercise per hour
28.5°C WBGT - Fixed Work Rate
For four hours, participants will walk on a treadmill to elicit 430 W of metabolic heat production in the following conditions: 28.5°C WBGT (34°C, 54% relative humidity) @ 15 min exercise per hour
35.5°C WBGT - Fixed Work Rate
For four hours, participants will walk on a treadmill to elicit 430 W of metabolic heat production in the following conditions: 35.5°C WBGT (40°C, 65% relative humidity) @ 15 min exercise per hour
26.0°C WBGT - Fixed work-to-rest ratio
For four hours, participants will walk on a treadmill at differing levels of metabolic heat production and environmental conditions (noted below), but at a fixed work-rest ratio of 30 minutes per hour. 26.0°C WBGT (31°C, 55% relative humidity) @ 530 W metabolic heat production
30.5°C WBGT - Fixed work-to-rest ratio
For four hours, participants will walk on a treadmill at differing levels of metabolic heat production and environmental conditions (noted below), but at a fixed work-rest ratio of 30 minutes per hour. 30.5°C WBGT (36°C, 55% relative humidity) @ 230 W metabolic heat production
30.5°C WBGT - Fixed work-to-rest ratio (high intensity)
For four hours, participants will walk on a treadmill at differing levels of metabolic heat production and environmental conditions (noted below), but at a fixed work-rest ratio of 30 minutes per hour. 30.5°C WBGT (36°C, 55% relative humidity) @ 530 W metabolic heat production

Locations

Country Name City State
United States School of Public Health Bloomington Indiana

Sponsors (2)

Lead Sponsor Collaborator
Indiana University State University of New York at Buffalo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Core body temperature Heat strain variable through study completion, up to 20 weeks
Other Mean skin temperature Heat strain variable through study completion, up to 20 weeks
Other Oxygen uptake Heat strain variable through study completion, up to 20 weeks
Other Heart rate Heat strain variable through study completion, up to 20 weeks
Other Blood pressure Heat strain variable through study completion, up to 20 weeks
Other Whole-body sweat rate Hydration and heat strain variable through study completion, up to 20 weeks
Other Percentage change in body weight Hydration status variable through study completion, up to 20 weeks
Other Plasma osmolality Hydration status variable through study completion, up to 20 weeks
Other Urine osmolality Hydration status variable through study completion, up to 20 weeks
Other Blood and plasma volume Hydration status variable through study completion, up to 20 weeks
Other Urine specific gravity Hydration status variable through study completion, up to 20 weeks
Other Plasma copeptin Hydration status variable through study completion, up to 20 weeks
Other Creatinine clearance Kidney function variable through study completion, up to 20 weeks
Other Fractional excretion of electrolytes Kidney function variable through study completion, up to 20 weeks
Other Free water clearance Kidney function variable through study completion, up to 20 weeks
Other Serum uric acid Kidney function variable through study completion, up to 20 weeks
Other Urinary uric acid Kidney function variable through study completion, up to 20 weeks
Primary Peak urinary [IGFBP7•TIMP-2] Kidney injury marker through study completion, up to 20 weeks
Secondary Urinary NGAL Kidney injury marker through study completion, up to 20 weeks
Secondary Urinary IGFBP7 Kidney injury marker through study completion, up to 20 weeks
Secondary Urinary TIMP-2 Kidney injury marker through study completion, up to 20 weeks
Secondary Urinary IL-18 Kidney injury marker through study completion, up to 20 weeks
Secondary Urinary L-FABP Kidney injury marker through study completion, up to 20 weeks
Secondary Renal artery blood velocity Index of kidney blood flow through study completion, up to 20 weeks
Secondary Segmental artery blood velocity Index of kidney blood flow through study completion, up to 20 weeks
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