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Clinical Trials/NCT03972007
NCT03972007
Unknown
Not Applicable

Effect of Light-emitting Diode (LED) Photobiomodulation Therapy on Muscular Fatigue in University Handball Athletes

University of Sao Paulo1 site in 1 country32 target enrollmentMay 18, 2019
ConditionsMuscular Injury

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Muscular Injury
Sponsor
University of Sao Paulo
Enrollment
32
Locations
1
Primary Endpoint
Difference in number of repetitions
Last Updated
5 years ago

Overview

Brief Summary

Introduction: Low-intensity laser therapy (LBI) is a therapeutic modality with a large number of clinical studies in recent years, taking into account its effectiveness in tissue repair, pain control and, more recently, to increase performance. It is known that LED therapy has immediate effects. Therefore, analyzing the TLED in the infrared spectrum for acute responses at different times along with fatigue resistance capabilities, heart rate variability and biochemical response to fatigue in handball athletes becomes necessary. Objective: To analyze the acute effects of LED phototherapy (940nm) on fatigue resistance and recovery after strenuous exercises of university athletes. Method: The study sample will consist of 32 and 36 male athletes, for biceps brachii and quadriceps femoris, respectively. The athletes will be randomly assigned into four groups: Immediate TLED (TLED-I), TLED 15Min (TLED-15), Immediate Sham (Sham-I) and Sham 15Min (Sham-15). The tests performed will involve bioimpedance evaluation, blood lactate, electromyographic analysis and evaluation of maximum voluntary contraction by means of the maximal repetition test (1RM). Thus, the TLED will be applied on the muscle group to be evaluated, unilaterally, the same tests being repeated in the sequence. For analysis of the data, normality test will be used to verify the distribution and adequate statistical tests for the appropriate intra and intergroup comparisons, being considered two factors in the comparisons, time and group. A significance level of 5% will be adopted.

Detailed Description

It is a blinded randomized clinical trial. The athletes will undergo a previous evaluation (day 1) comprised by anamnesis and evaluation of the bioimpedance to analyze the body composition, will still carry out the evaluation of the load for a maximum repetition. Thus, 7 days after (day 2) the previous evaluation in the times immediately after and after 15 minutes of the LED application will be carried out new tests. These will involve assessment of blood lactate, heart rate variability and electromyography. In addition, during the execution of the fatigue protocol will be collected the number of repetitions of muscle contraction and its total execution time. Due to the number of athletes that make up the university team (n = 19), cross-over will be necessary, where all athletes will initially be distributed to the 04 pre-defined groups in each subproject, and after the 7 days, they will be divided again.

Registry
clinicaltrials.gov
Start Date
May 18, 2019
End Date
October 1, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rinaldo Roberto de Jesus Guirro

Director

University of Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • Handball practitioners;
  • Absence of musculoskeletal injury in the last three months;
  • Absence of anti-inflammatory and / or analgesic drugs 72 hours before the evaluations

Exclusion Criteria

  • Use of anabolic steroids;
  • Presence of cardiovascular disease
  • Use of alcohol and illicit drugs during the collection period

Outcomes

Primary Outcomes

Difference in number of repetitions

Time Frame: 2 years

The present study was designed to detect the difference in the number of repetitions between the groups groups, after the interventions.

Study Sites (1)

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