Thermodynamic Exposure and Sleep in Military Cadets
Hot, Cold, and Combined Thermodynamic Exposure to Improve Sleep Quality and Sleep-Time Glymphatic Clearance Among Military Cadets
1 other identifier
interventional
45
1 country
1
Brief Summary
This pilot study investigates the effects of cold-water immersion, traditional sauna use, and their combination on sleep architecture, glymphatic clearance, and psycho-affective health in military cadets. The study uses wearable technologies including the Oura Ring and the Applied Cognition Glymphatic Monitor to collect objective sleep and physiological data.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 12, 2025
CompletedFirst Posted
Study publicly available on registry
October 1, 2025
CompletedStudy Start
First participant enrolled
April 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 1, 2026
March 13, 2026
March 1, 2026
6 months
September 12, 2025
March 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Glymphatic clearance
Changes in parenchymal resistance during sleep
End of baseline monitoring phase (Day 7), end of intervention week 1 (Day 14), and end of intervention (Day 28)
Sleep Efficiency
Percentage of sleep period spent asleep measured by the Oura Ring (percentage, %)
Each night of the baseline monitoring period (7days) and intervention phase (14days)
Pittsburgh Sleep Quality Index
Self-reported sleep quality
At the end of the baseline monitoring phase (Day 7), end of intervention week 1 (Day 14), and end of intervention phase (Day 28)
Profile of Mood States: Total Mood Disturbance
Self-reported mood disturbance used by summing all negative profiled mood sub-scores (tension, depression, anger/hostility, fatigue, and confusion) and subtracting the positive profiled mood sub-score (vigor). (score -32 - 200, higher equals greater mood disturbance)
At the end of the baseline monitoring phase (Day 7), end of intervention week 1 (Day 14), and end of intervention phase (Day 28)
Secondary Outcomes (15)
Total Sleep Duration
Each night of the baseline monitoring period (7days) and intervention phase (14days)
REM Sleep Duration
Each night of the baseline monitoring period (7days) and intervention phase (14days)
Deep Sleep Duration
Each night of the baseline monitoring period (7days) and intervention phase (14days)
Light Sleep Duration
Each night of the baseline monitoring period (7days) and intervention phase (14days)
Restless Sleep Duration
Each night of the baseline monitoring period (7days) and intervention phase (14days)
- +10 more secondary outcomes
Study Arms (3)
Cold-water immersion
EXPERIMENTAL5 minutes of cold-water immersion (submerged up to chin) at 8 - 10C°(46.4 - 50F°) in the morning between 6:00 - 8:00am.
High heat sauna
EXPERIMENTAL20 minutes of high heat sauna at 90 - 94C° (190 - 201.2F°) between 5:00 - 7:00pm
Combination
EXPERIMENTAL5 minutes of cold-water immersion (submerged up to chin) at 8 - 10C°(46.4 - 50F°) in the morning between 6:00 - 8:00am and 20 minutes of high heat sauna at 90 - 94C° (190 - 201.2F°) between 5:00 - 7:00pm
Interventions
Participants will complete 14 daily sessions of cold-water immersion exposure.
Participants will complete 14 evening sessions in the high heat sauna
Eligibility Criteria
You may qualify if:
- years of age
- Member of the Ranger Challenge group at The Citadel.
- Access to a smartphone with access to appropriate app marketplace (Apple iOS 15, Android 8.0 or newer) and reliable data access.
- Ability to access and operate Oura Ring application
You may not qualify if:
- Medical contraindications to continuous wearing of the Oura Ring.
- Current diagnosis of neurological, cardiovascular, and/or sleep disorder.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Citadel Military College
Charleston, South Carolina, 29404, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mark Rosenberg, MD
Medical University of South Carolina
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 12, 2025
First Posted
October 1, 2025
Study Start
April 1, 2026
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
October 1, 2026
Last Updated
March 13, 2026
Record last verified: 2026-03