Cold Water Immersion on Recovery and Performance
A Prospective Crossover Trial in NCAA Division I Athletes Using Continuous WHOOP Biometrics
About this conference presentation
Historical, unpublished findings: This page records the AMSSM 2025 presentation. Its preliminary results and exploratory subgroup analyses should not be treated as current peer-reviewed conclusions or a validated method for choosing individual recovery treatments. Read the published evidence review.
Cold water immersion (CWI) is widely used by athletes for post-exercise recovery, but meta-analyses of the general population show variable effects. This study asked a more targeted question: which athletes actually respond to CWI, and can wearable biometrics identify them? Using a prospective crossover design with continuous WHOOP monitoring, we tracked heart rate variability (HRV), resting heart rate (RHR), subjective recovery, and muscle soreness in 37 NCAA Division I athletes across CWI and control conditions.
Findings reported at AMSSM 2025
Preliminary conference results from 37 NCAA Division I athletes. Subgroup findings are exploratory.
Takeaway
These preliminary conference findings generated questions about individual responses to cold water immersion. They do not establish a reproducible responder subgroup or prove that a nonsignificant performance finding means no impairment. Interpret them alongside the published recovery evidence and its limitations.
Intervention Protocol
- Modality: Cold water immersion (CWI), performed post-training
- Temperature: Approximately 53°F (11.7°C)
- Duration: 10 minutes per session
- Frequency: 5 sessions per week
- Total Intervention: 4-week crossover period
- Monitoring: Continuous WHOOP biometric tracking throughout
Outcome Measures
- Heart Rate Variability (HRV): Nightly via WHOOP, weekly averages
- Resting Heart Rate (RHR): Nightly via WHOOP
- Subjective Recovery: Daily WHOOP recovery score (0–100%)
- Muscle Soreness (DOMS): Daily Likert-scale self-report
- Countermovement Jump: Baseline and post-intervention, force plate
Authors & Research Team
View on ClinicalTrials.gov
Access the full study record, protocol details, and enrollment status.
NCT06565468Want to get involved?
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