The Effects of Cold Water Immersion With Different Dosages (Duration and Temperature Variations) on Heart Rate Variability Post-exercise Recovery

NCT02499640 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-07-16

No results posted yet for this study

Summary

The aim of the present study was to investigate the effects of cold water immersion (CWI) during post-exercise recovery with different durations and temperatures on heart rate variability (HRV) indices. 100 participants performed a protocol of jumps and a Wingate test, and immediately afterwards were immersed in cold water, according to the characteristics of each group (CG: control; G1: 5' at 9±1°C; G2: 5' at 14±1°C; G3: 15' at 9±1°C; G4: 15' at 14±1°C). Analyses were performed at baseline, during the recuperative technique (TRec) by CWI and 20, 30, 40, 50 and 60 minutes post-exercise. The HRV indices average of all RR intervals in each analysis period (Mean RR), standard deviation of normal R-R intervals (SDNN), square root of the mean of the sum of the squares of differences between adjacent R-R intervals (RMSSD), spectral components of very low frequency (VLF), low frequency (LF) and high frequency (HF), scatter of points perpendicular to the line of identity of the Poincaré Plot (SD1) and scatter points along the line of identity (SD2) were assessed. Comparisons between groups and moments were performed using the technique of analysis of variance for repeated measures in two scheme factors. A significance level of p\<0.05 was considered.

Conditions

  • Cryotherapy Effect

Interventions

OTHER

immersion cold water

immersion cold water at different temperatures and exposure times

Sponsors & Collaborators

  • Paulista University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2015-05-31
Completion
2015-05-31

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Read the full study record

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View NCT02499640 on ClinicalTrials.gov