RecruitingNot ApplicableNCT07224646

Whole-Body Photobiomodulation Use in Professional Soccer Players During a State Championship

Sponsor

Universidade Federal de Sao Carlos

Enrollment

24 participants

Start Date

Sep 4, 2025

Study Type

INTERVENTIONAL

Conditions

Athletic Performance Muscle Fatigue Muscle Strength Sports

Summary

This study aims to investigate the effects of whole-body photobiomodulation on professional soccer players during a state championship. The primary question is whether photobiomodulation improves recovery, reduces muscle fatigue, and enhances performance compared to standard training without photobiomodulation.

Eligibility

Sex: MALEMin Age: 18 YearsMax Age: 35 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Sham PBM and Whole-Body Photobiomodulation (PBM) (Active PBM) for people with athletic performance, muscle fatigue, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include men aged 18 Years to 35 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONWhole-Body Photobiomodulation (PBM) (Active PBM)

This intervention consists of whole-body photobiomodulation delivered using a full-body PBM device. Sessions are performed twice weekly on non-consecutive days for 8 weeks, coinciding with the athletes' standard training. The device emits therapeutic light at specified wavelengths and power, targeting the entire body. The protocol is standardized according to prior research, ensuring consistent exposure for all participants in the active arm. The intervention aims to improve muscle performance and recovery while reducing delayed onset muscle soreness (DOMS).

RADIATIONSham PBM

Intervention Description (Sham PBM): Participants receive a sham photobiomodulation intervention using the same device and schedule, but without emission of therapeutic light. The procedure mimics the active intervention to maintain blinding while allowing comparison of outcomes, including muscle performance, DOMS, and blood markers.