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ight therapy and electrical stimulation on functional performance in volleyball athletes

Not Applicable
Recruiting
Conditions
Athletic Performance, muscle Weakness.
C05.651.515
Registration Number
RBR-27kdyf
Lead Sponsor
niversidade Federal de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

Healthy volunteers; volleyball players; gender male; non-smoking; aged between 17 and 18; weight within 15% variation limit of normal weight for male athletes, taking into account height and physique.

Exclusion Criteria

smoking volunteers; history of alcohol or substance abuse; diagnosis of cardiac, renal, gastrointestinal, hepatic, pulmonary, neurological, psychiatric, hematological or metabolic disorders; that are not available to participate in all stages of the study.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Athletes have muscular strength of knee extension of dominant and non-dominant assessed by dynamometry, from a range of at least 10% in the pre-intervention ( 24 hours prior to intervention) and post intervention (24 hours after completion of the intervention).<br>Athletes have jump height measured by the maximum range of the test from a variation of at least 10% in preintervention ( 24 hours prior to intervention) and post intervention (24 hours after completion of the intervention).
Secondary Outcome Measures
NameTimeMethod
Athletes have the perception of the global effect of the jump evaluated through a subjective perception scale as it classifies tried his heels in these days, and can respond on a scale al -5 to +5 variation or very much worse better, from a variation of at least 10% in the pre-intervention ( 24 hours prior to intervention) and post intervention (24 hours after completion of the intervention).<br>Athletes have evaluated the amount of jumps through the maximum number of hops test within two minutes from a range of at least 10% in the pre-intervention ( 24 hours prior to intervention) and post intervention (24 hours after completion of the intervention).
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