Health Behavior Clinical Trial
Official title:
Cold Water Immersion in the Recovery of Clinical, Biochemical, Functional and Neuromuscular Markers of Muscle Damage of 10km Street Runners: Clinical, Randomized and Blinded Trial
| Verified date | April 2017 |
| Source | Universidade Federal do Rio Grande do Norte |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Objective: To analyze the effect of cold water immersion (CWI) on the recovery of clinical,
biochemical, functional and neuromuscular markers of muscle damage in 10 km street runners.
Materials and Methods: This is a randomized, blinded trial in which 30 subjects, 10 km
street runners, were randomly divided into three groups: control (gC), immersion (gI) and
CWI (gCWI). The runners will be evaluated for clinical (subjective perception of exertion),
biochemical (serum CK), functional (unipodal triple hop distance and shuttle test time) and
neuromuscular variables by means of isokinetic variables (peak torque, total work and
fatigue index). Volunteers will perform pre-assessment, immediately post-race and
post-intervention, and 24-hour post-intervention. The data will be expressed by mean and
standard deviation, analyzed in the statistical package SPSS 20.0. A significance level of
5% and a 95% confidence interval will be considered for all measures.
| Status | Active, not recruiting |
| Enrollment | 30 |
| Est. completion date | April 2017 |
| Est. primary completion date | April 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Male |
| Age group | 20 Years to 40 Years |
| Eligibility |
Inclusion Criteria: - Body Mass Index between 18.5 and 30 kg/m2; - Street runners for at least 6 months; - Week frequency of at least 3 times; - Do not present cardiopathies, muscles and neurological diseases; Exclusion Criteria: - Hypersensitivity or allergies to cryotherapy; - Unable to complete the 10 km event on the day of the evaluation; - Do not complete or perform any of the study procedures for any reason (phobias, do not withstand the exposure time). |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Universidade Federal do Rio Grande do Norte |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Subjective perception of pain. | The subjective perception of pain will be measured by means of the visual analogic scale based on the self-report of the level of pain. | Up to 10 weeks |
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