Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
15 participants
INTERVENTIONAL
2022-03-21
2023-11-05
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
PREVENTION
NONE
Study Groups
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40:20
Walking for 40 minutes, resting for 20
Work to rest cycles of 40:20 minutes
Walking in a hot environment for 2 hours with repeated 40 minutes of work and 20 minutes of rest
20:10
Walking for 40 minutes, resting for 20
Work to rest cycles of 20:10 minutes
Walking in a hot environment for 2 hours with repeated 20 minutes of work and 10 minutes of rest
Interventions
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Work to rest cycles of 40:20 minutes
Walking in a hot environment for 2 hours with repeated 40 minutes of work and 20 minutes of rest
Work to rest cycles of 20:10 minutes
Walking in a hot environment for 2 hours with repeated 20 minutes of work and 10 minutes of rest
Eligibility Criteria
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Inclusion Criteria
* Physically active
Exclusion Criteria
* Hypertensive or tachycardic during the screening visit (systolic blood pressure ≥ 140 mmHg, diastolic blood pressure ≥ 90 mmHg, resting heart rate ≥ 100 bpm)
* Taking medication or supplements with a known side effect of affecting physiologic responses to exercise (e.g., acetaminophen, beta blockers, statins, aspirin)
* Any form of tobacco or nicotine use in the past six months
* Current musculoskeletal injury impacting physical activity
* A positive pregnancy test at any point in the study
* Study physician discretion based on any other medical condition or medication
18 Years
39 Years
ALL
Yes
Sponsors
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State University of New York at Buffalo
OTHER
Responsible Party
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Riana Pryor
Assistant Professor
Principal Investigators
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Riana Pryor, PhD
Role: PRINCIPAL_INVESTIGATOR
University at Buffalo
Locations
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University at Buffalo
Buffalo, New York, United States
Countries
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Other Identifiers
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STUDY00006115
Identifier Type: -
Identifier Source: org_study_id
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