An interventional study of Standard work pace and Additional rest breaks in Hyperthermia, Fatigue; Heat and Work-Related Condition, sponsored by State University of New York at Buffalo. Not yet recruiting. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-30.
Sponsored by State University of New York at Buffalo · Not applicable, Interventional, and Prevention
The goal of this project is to compare different ways to schedule a workday to see if older workers should follow a specific work protocol to reduce strain on the heart and muscles across two consecutive days of work.
Participants will come to the lab a total of six times. During four of the visits participants will complete a box carrying task, simulating unloading a delivery truck. This will take place in a hot and humid room to simulate being outdoors during the summer.
256 studies on the registry are indexed under Hyperthermia; 73 are open to participants now.
This study's planned enrollment of 32 is below the median of 40 across 232 interventional studies indexed under Hyperthermia.
Browse Hyperthermia studies →State University of New York at Buffalo is the lead sponsor of 294 studies on the registry; 63 are open to participants now.
Of its 19 completed or terminated interventional studies of FDA-regulated products, 15 (79%) have results posted.
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Exclusion Criteria:
The order of the interventions is standard work pace first, followed by the rest trial second.
Behavioral: Standard work pace · Behavioral: Additional rest breaks
The order of the interventions is the additional rest breaks first and the standard work pace second.
Behavioral: Standard work pace · Behavioral: Additional rest breaks
On two consecutive days, participants will work at a standard pace of one box per minute during the box carrying protocol
On two consecutive days, participants will work at the standard work pace during the box carrying protocol and have superimposed 5 minutes of rest every 30 minutes.
Cardiac Troponin
Serum cardiac troponin concentration
Time frame: 2 hours following work protocol, approximately 6 hours into the trial
Maximum Core Temperature
Highest core temperature attained during the work protocol
Time frame: End of work protocol, approximately 4 hours into the trial
No study locations are listed for this record.
Plan to share: Yes — A spreadsheet of the cleaned, de-identified individual data for all variables will be shared on at clinicaltrials.gov without restriction to ensure public availability. Individual data will be identified using unique participant identifier numbers. In addition to the datasets, a study protocol, data dictionary defining and describing all variables, and data collection instruments will be shared and associated with the relevant datasets.
Supporting information: Study protocol
Time frame: Data from this project will be made available as soon as able and no later than the time of the final publication. Original data will be preserved indefinitely after the end of the funding period.
Access criteria: Pooled and de-identified data will be made available to interested researchers upon email request.
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.
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State University of New York at Buffalo →