Thermodynamic Exposure and Sleep in Military Cadets
Hot, Cold, and Combined Thermodynamic Exposure to Improve Sleep Quality 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 and psychological health in military cadets. The study uses wearable technologies including the Oura Ring 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 Jul 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
July 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2027
May 19, 2026
May 1, 2026
6 months
September 12, 2025
May 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
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)
Brief Mood Introspection Scale
Self-reported assessment of mood consisting of 16 mood adjectives. Participants rate each adjective on a 4-point likert scale (0 = definitely don't feel, 3 = definitely feel). The assessment captures 2 core dimensions of mood valence (pleasant v. unpleasant) and arousal (active v. calm).
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 (9)
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)
- +4 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:
- \. 18 - 30 years of age 2. Enrolled military cadet at the Citadel Military College. 3. Access to a smartphone with access to appropriate app marketplace (Apple iOS 15, Android 8.0 or newer) and reliable data access.
You may not qualify if:
- Medical contraindications to continuous wearing of the Oura Ring.
- Current diagnosis of neurological conditions that impact vascular blood flow or the individual's ability to regulate temperature.
- History of cardio-vascular conditions or history of poor blood circulation.
- History of heat stroke or known sensitivity to hot/cold environments.
- Currently taking medications that impair fluid balance, thermoregulation, blood flow, respiration, or heart rate.
- Known dermatological disease aggravated by changes in temperature.
- Pregnant or trying to become pregnant within the study timeframe. Urine samples will be provided by interested female cadets to ensure they are not pregnant.
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
July 1, 2026
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
May 1, 2027
Last Updated
May 19, 2026
Record last verified: 2026-05