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CrossfitĀ® is a method of strength training and fitness built on functional movements, constantly varied and executed at high intensity. Competitions such as the CrossfitĀ® involve physically demanding activities, which in addition to being performed at high intensity also use great measures of aerobic capacity related with performance. These characteristics cause metabolic and muscular stress, as well as a decrease in physical performance. The demand for intensity is the cause of concern regarding the practice of CrossfitĀ® and the risk of injuries. Studies using photobiomodulation therapy combined with static magnetic fields (PBMT/sMF) to delay fatigue and increase performance have obtained positive results in different types of exercise and application times. However, there are no studies investigating the effects of PBMT/sMF in training with similar characteristics as CrossfitĀ®. Therefore, the aim of this project is to verify the effects of PBMT/sMF on performance and muscle recovery of CrossfitĀ® athletes at different times of application (pre workout of the day [WOD] and/or post WOD) in order to determine the best way to use the therapy.
To achieve the proposed objective it will be performed a randomized, crossover, triple-blind (volunteers, outcome assessors and therapists), placebo-controlled trial.
Twelve volunteers will be allocated to four interventions/situation. The order of the interventions/situations will be randomized.
The volunteers will be treated by a blinded therapist.
The outcomes will be obtained at baseline (prior to WOD), and 1 hour, 24 and 48 hours after WOD. Except for the ratings of perceived exertion that will be obtained at baseline, after WOD, and 1 hour, 24 and 48 hours after WOD. In addition, for the functional analysis the data will be collected at baseline, after applied intervention, and 1 hour, 24 and 48 hours after WOD. The data will be collected by a blinded assessor.
The WOD will be consisted in finish as quickly as possible a sequence of three exercises (Calories in Assault AirBikeĀ®, Hang Squat Clean and Box Jump Over), in a well-known series model for the athletes, without rest.
The investigators will analyze: ratings of perceived exertion; activity of creatine kinase (CK); levels of the cytokine Interleukin-6 (IL-6), and maximum number of free squat reps in 1 minute.
Statistical analysis:
All data will be analyzed both in their absolute values and in relation to their percentage variation from the values obtained in the pre-WOD (baseline) assessments. The results obtained will be tested for normality using the Kolmogorov-Smirnov test. If data show normal distribution, the ANOVA test (one or two way depending on the outcome analyzed) with post-hoc Bonferroni will be used. The level of statistical significance will be p<0.05.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Effective PBMT/sMF before WOD and Placebo PBMT/sMF after WOD | Experimental | PBMT/sMF will be applied in two steps: effective PBMT/sMF will be applied before the WOD and placebo PBMT/sMF will be applied after the WOD. |
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| Placebo PBMT/sMF before WOD and Effective PBMT/sMF after WOD | Experimental | PBMT/sMF will be applied in two steps: placebo PBMT/sMF will be applied before the WOD and effective PBMT/sMF will be applied after the WOD. |
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| Effective PBMT/sMF before WOD and Effective PBMT/sMF after WOD | Experimental | PBMT/sMF will be applied in two steps: effective PBMT/sMF will be applied before the WOD and effective PBMT/sMF will be applied after the WOD. |
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| Placebo PBMT/sMF before WOD and Placebo PBMT/sMF after WOD. | Placebo Comparator | PBMT/sMF will be applied in two steps: placebo PBMT/sMF will be applied before the WOD and placebo PBMT/sMF will be applied after the WOD. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Effective PBMT/sMF | Device | A cluster with 20 diodes, manufactured by Multi Radiance MedicalĀ® (Solon, OH, USA), will be used: 4 diodes of 905 nm (1.25 average power, 50 W of peak power for each diode), 8 diodes of 850 nm (40 mW of average power for each diode) and 4 diodes of 633 nm (25 mW average power for each diode). Effective PBMT/sMF will be applied in direct contact with the skin and light pressure in: 4 sites in the knee extensor/hip flexor muscles, 3 sites in the knee flexor/hip extensor muscles and 1 site in the plantar flexor muscles. The effective PBMT/sMF will be applied to both lower limbs. The dose used for applications will be approximately 270 J for knee extensors/hip flexors, 180 J for knee flexors/hip extensors, and 60 J for plantar flexors. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in functional capacity | The functional capacity will be measured by a maximum number of free squat repetitions within 1 minute. | 1 minute post-treatment, 1hour, 24 hours and 48 hours after WOD (workout of the day). |
| Measure | Description | Time Frame |
|---|---|---|
| Perception of exercise intensity | The perception of exercise intensity will be measured by a 0-100 Ratings of Perceived Exertion Scale: in this scale lower score, means lower degree of fatigue and higher score, means higher degree of fatigue. | 1 minute after WOD, 1 minute post-treatment, 1 hour, 24 hours and 48 hours after WOD (workout of the day). |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Ernesto Cesar Pinto Leal Junior, PhD | University of Nove de Julho | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Laboratory of Phototherapy and Innovative Technologies in Health | SĆ£o Paulo | 01504-001 | Brazil |
Data will be shared upon request addressed to the principal investigator
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The volunteers will be allocated to four interventions/situation:
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A researcher will program the device (placebo or PMBT) and will be instructed not to inform the volunteers or other researchers as to the type of treatment (PMBT or placebo). Therefore, the researcher responsible for the treatment will be blinded to the type of treatment being administered to the volunteers. The sounds and signals emitted from the device as well as the information displayed on the screen will be identical, regardless of the type of treatment (placebo or PBMT).
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| Placebo PBMT/sMF | Device | A cluster manufactured by Multi Radiance MedicalĀ® (Solon, OH, USA) with 20 diodes will be used: Placebo PBMT/sMF will be applied in direct contact with the skin and light pressure in: 4 sites in the knee extensor/hip flexor muscles, 3 sites in the knee flexor/hip extensor muscles and 1 site in the plantar flexor muscles. The placebo PBMT/sMF will be applied to both lower limbs. The dose used for applications will be approximately 0 J per diode. The sounds and signals emitted from the device as well as the information displayed on the screen will be identical, regardless of the type of treatment (active or placebo). |
|
| Activity of creatine kinase (CK) | The activity of CK will be analyzed by spectrophotometry and using specific reagent kits from the blood samples collected. | 1 hour, 24 hours and 48 hours after WOD (workout of the day). |
| Levels of interleukin-6 (IL-6) | The levels of interleukin-6 will be analyzed by enzyme-linked immunosorbent assay (ELISA) and using specific reagent kits from the blood samples collected. | 1 hour, 24 hours and 48 hours after WOD (workout of the day). |