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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03094689
Other study ID # 1.441.252
Secondary ID
Status Active, not recruiting
Phase N/A
First received January 5, 2017
Last updated April 27, 2017
Start date January 2017
Est. completion date April 2017

Study information

Verified date April 2017
Source Universidade Federal do Rio Grande do Norte
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cold water immersion

Water immersion


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal do Rio Grande do Norte

Outcome

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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