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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
783 participants
OBSERVATIONAL
2021-06-11
2025-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The aim of this study is to examine traditional and novel risk factors that may increase thermal strain and EHI likelihood in military recruits undergoing strenuous physical exercise.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparing Exertional Heat Illness Risk Factors Between Patients and Controls
NCT05303142
Study of Risk Factors for the Occurrence and Severity of Exertional Heatstroke in the Military Environment
NCT04593316
Exertional Heat Illness: Biomarkers for Prediction and Return to Duty
NCT01434979
Physiological Responses to Heat Stress During High-risk Events
NCT06907225
Study of Biomarkers of Heat Tolerance and Recovery During Ultra-endurance Exercise
NCT05921864
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exertional heat illness
Participants who experience an atypical elevation in thermal strain or an EHI undergoing strenuous physical exercise.
Core temperature monitoring
Core temperature will be monitored on the day of exercise
Questionnaires
Questionnaires will be completed at baseline and on the day of exercise
Heart rate monitoring
Heart rate will be monitored on the day of exercise
Urine collection
Urine samples will be collected at baseline and on the day of exercise
Sleep monitoring
Sleep will be monitored at baseline and on the day of exercise
Blood collection
Blood samples will be completed at baseline
Saliva collection
Saliva samples will be collected at baseline and on the day of exercise
Throat swab collection
Throat swab samples will be collected at baseline and on the day of exercise
Stool collection
Stool samples will be collected at baseline and on the day of exercise
Control
Participants who do not experience an atypical elevation in thermal strain or an EHI undergoing strenuous physical exercise.
Core temperature monitoring
Core temperature will be monitored on the day of exercise
Questionnaires
Questionnaires will be completed at baseline and on the day of exercise
Heart rate monitoring
Heart rate will be monitored on the day of exercise
Urine collection
Urine samples will be collected at baseline and on the day of exercise
Sleep monitoring
Sleep will be monitored at baseline and on the day of exercise
Blood collection
Blood samples will be completed at baseline
Saliva collection
Saliva samples will be collected at baseline and on the day of exercise
Throat swab collection
Throat swab samples will be collected at baseline and on the day of exercise
Stool collection
Stool samples will be collected at baseline and on the day of exercise
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Core temperature monitoring
Core temperature will be monitored on the day of exercise
Questionnaires
Questionnaires will be completed at baseline and on the day of exercise
Heart rate monitoring
Heart rate will be monitored on the day of exercise
Urine collection
Urine samples will be collected at baseline and on the day of exercise
Sleep monitoring
Sleep will be monitored at baseline and on the day of exercise
Blood collection
Blood samples will be completed at baseline
Saliva collection
Saliva samples will be collected at baseline and on the day of exercise
Throat swab collection
Throat swab samples will be collected at baseline and on the day of exercise
Stool collection
Stool samples will be collected at baseline and on the day of exercise
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
17 Years
35 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Institute of Naval Medicine (UK)
UNKNOWN
CTCRM Lympstone (UK)
UNKNOWN
University of Portsmouth (UK)
UNKNOWN
Public Health Wales
OTHER_GOV
Bangor University (UK)
UNKNOWN
Headquarters Army Recruiting and Initial Training Command (UK)
UNKNOWN
Defence Science and Technology (UK)
UNKNOWN
Liverpool John Moores University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Commando Training Centre Royal Marine
Lympstone, Devon, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2029/MODREC/21
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.