Background: Photobiomodulation has been explored for years, with wide clinical use for wound healing and analgesia in varied orthopedic conditions, but the number of research and clinical use has increased during the last decade. Furthermore, considering the performance, the current literature is conflicting and restricted, with divergences in wavelength, power and energy density applied. Therefore, analyze different doses for a answer in short and long time, associated with capacities of strength, fatigue resistance and functional performance of handball players becomes necessary. Objective: To analyze the effects of the application of LED phototherapy on the capacities of strength, functional efficiency, temperature and fatigue resistance of handball players.Method: The study sample will be composed of 56 male handball players randomly allocated into four groups: LED 50J (G-50J), LED 240J (G-240J), LED 50-240J (G-50-240J) – progressive dose and Sham (G-S). The athletes will be submitted to a evaluations of muscle performance and functional performance, metabolic and physiological evaluation. After initial tests, in six consecutives weeks the LEDT (940nm – infrared) will be applied to the quadriceps femoris muscle and hamstrings, bilaterally, associated with a muscle strength protocol. Also, at the end of the second and fourth week there will be evaluations of muscular, metabolic and physiological performance. After 24 hours of the last application TLED the tests will be repeated. Seven days after the last intervention will be performed a follow-up. For analysis, 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.
- Study Type: Interventional
- Study Design
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Primary Purpose: Other
- Masking: Triple (Participant, Investigator, Outcomes Assessor)
- Study Primary Completion Date: October 1, 2021
It is a blinded randomized clinical trial. The athletes will undergo pre-evaluation, 6 weeks of training associated with LED application, being distributed in two applications per week and a re-evaluation 24 hours after the last application, totaling a total of approximately 8 weeks. Thus, on the first day (Pre-test) athletes will be submitted to anthropometric evaluation, blood sample collection for evaluation of basal blood lactate levels, as well as evaluation by bioimpedance for analysis of detailed body composition. Then, the maximum voluntary contraction test (CVM) will be performed on the isokinetic dynamometer, together with the electromyographic evaluation. Before and after the evaluation with the isokinetic dynamometer, thermography and plethysmography will be collected.
After 24 hours, the vertical jump test will be performed and after 15 minutes of passive rest, the athlete will perform the incremental test.
After the initial evaluations, the researcher will go to the training center of the team to apply the respective interventions, which consist of applying LEDs all over the quadriceps and hamstring bilaterally, while the sham group (GS) will receive the LED application off, without the emission of light. The application will occur for six weeks, and will occur twice weekly, on days spaced for at least 48 hours. The same will be done in conjunction with the lower limb strength training protocol.
The tests performed at the time of pre-application of the LED (Pre-test) will be reapplied in the same order 24 hours after the last application of the interventions. The isokinetic evaluation, together with electromyography, plethysmography and thermography of the quadriceps bilaterally, will also be performed after two and four weeks of intervention. After seven days of the last application, the isokinetic evaluation, electromyography, vertical jump evaluation and incremental test will be performed. In addition, at the end of the second and fourth week the volunteer will carry out an evaluation with the isokinetic dynamometer, electromyography, plethysmography and thermography.
- Other: Photobiomodulation
- An LED blanket with 267 infrared lamps with predetermined doses will be used, given a wavelength of 940nm, for 6 weeks, it will be applied by all extension of the quadriceps and hamstrings bilaterally, just before the force training protocol for the groups intervention or simulation for the sham group. Photochemical or photophysical effects are expected from its application.
Arms, Groups and Cohorts
- Sham Comparator: Sham Group (G-S)
- The LED will be positioned across the quadriceps and hamstring bilaterally, however, there will be no light emission. However, the athlete will perform the strength training protocol.
- Experimental: 50J Infrared LED Group (G-50J)
- The LED with a wavelength of 940nm, 50J power, will be applied throughout the quadriceps and hamstrings bilaterally, just before the strength training protocol.
- Experimental: 240J Infrared LED Group (G-240J)
- The LED with a wavelength of 940nm, 240J power, will be applied across the quadriceps and hamstrings bilaterally, just before the strength training protocol.
- Experimental: Progressive dose infrared LED group (G-50-240J)
- The LED with a wavelength of 940nm, initial energy of 50J with an increment of 38J each week to the final energy of 240J, will be applied throughout extension of the quadriceps and hamstrings bilaterally, immediately prior to the performance of the strength training protocol
Clinical Trial Outcome Measures
- difference of maximal voluntary contraction
- Time Frame: 3 years
- The study was designed to detect a difference of maximal voluntary contraction between the groups, following the interventions
Participating in This Clinical Trial
- Handball players;
- Participation of at least one official match in the last year and attend 70% of the team's activities during the current season.
- musculoskeletal injury in the last three months;
- cardiovascular diseases;
- use of anabolic, anti-inflammatory and analgesic drugs 72 hours before the evaluations;
- use of alcohol and illicit drugs during the collection period;
Gender Eligibility: Male
Minimum Age: 18 Years
Maximum Age: 40 Years
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
- Lead Sponsor
- University of Sao Paulo
- Provider of Information About this Clinical Study
- Principal Investigator: Rinaldo Roberto de Jesus Guirro, Professor – University of Sao Paulo
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