ClinicalTrials.Veeva

Menu

Effects of Photobiomodulation Therapy Combined With Static Magnetic Field in CrossFit® Athletes

U

University of Nove de Julho

Status

Completed

Conditions

Muscle Strength

Treatments

Device: Placebo PBMT/sMF
Device: Effective PBMT/sMF

Study type

Interventional

Funder types

Other

Identifiers

NCT04349085
3.360.743

Details and patient eligibility

About

Crossfit® is a method of strength training and fitness built on functional movements, constantly varied and executed at high intensity. Competitions such as the Crossfit® 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 Crossfit® 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 Crossfit®. Therefore, the aim of this project is to verify the effects of PBMT/sMF on performance and muscle recovery of Crossfit® 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.

Full description

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 AirBike®, 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.

Enrollment

12 patients

Sex

Male

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Crossfit® amateur male athletes;
  • who did not present a history of musculoskeletal injury in the regions of the hips, knees and calves in the month preceding the study;
  • who were not using pharmacological agents;
  • athletes should have been practicing the sport for at least 1 year;
  • voluntarily commit to participate in all stages.

Exclusion criteria

  • who presented musculoskeletal or joint injuries during data collection.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

12 participants in 4 patient groups, including a placebo group

Effective PBMT/sMF before WOD and Placebo PBMT/sMF after WOD
Experimental group
Description:
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.
Treatment:
Device: Placebo PBMT/sMF
Device: Effective PBMT/sMF
Placebo PBMT/sMF before WOD and Effective PBMT/sMF after WOD
Experimental group
Description:
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.
Treatment:
Device: Placebo PBMT/sMF
Device: Effective PBMT/sMF
Effective PBMT/sMF before WOD and Effective PBMT/sMF after WOD
Experimental group
Description:
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.
Treatment:
Device: Effective PBMT/sMF
Placebo PBMT/sMF before WOD and Placebo PBMT/sMF after WOD.
Placebo Comparator group
Description:
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.
Treatment:
Device: Placebo PBMT/sMF

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems