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The goal of this clinical trial is to evaluate the impact of different passive post-effort recovery techniques on professional athletes. The main questions it aims to answer are:
-Do passive recovery modalities significantly improve muscle oxygenation and tissue temperature immediately after high-intensity effort? Which specific technique is most effective in reducing perceived pain (pressure pain threshold) and restoring muscle strength?
Researchers will compare six different therapeutic interventions-TECAR therapy, massage, intermittent negative pressure (cupping), shockwave therapy, percussion guns, and pressotherapy-to see which provides the superior immediate physiological and functional recovery effect. Participants will:
Perform a high-intensity physical effort designed to induce peripheral fatigue.Be randomly assigned to receive one of the six recovery protocols.Undergo objective measurements immediately after the intervention, including muscle oxygen saturation (NIRS), tissue thermography, algometry, and dynamometry.
Full description
This project consists of a randomized, double-blind (tester and statistician), crossover clinical trial. The study aims to address the critical need for evidence-based recovery strategies in high-demand sports like basketball, where muscle overload is a primary risk factor for injuries.The investigation will focus on the immediate effects of six widely used physiotherapy modalities:
TECAR Therapy: Used to improve perfusion and modulate inflammation through deep tissue heating.
Percussive Massage (Massage Guns): Applied to reduce stiffness and enhance explosive force through mechanical vibration.
Shockwave Therapy (ESWT): Evaluated for its capacity to improve muscular microcirculation and accelerate tissue regeneration.
Pressotherapy (External Pneumatic Compression): Targeting the reduction of pain and the sensation of heaviness in the lower limbs.
Intermittent Negative Pressure (Cupping): Investigated for its role in improving blood flow and pain modulation Sports Massage: The traditional manual intervention for reducing delayed onset muscle soreness (DOMS) and improving flexibility. Physiological monitoring will be conducted using Near-Infrared Spectroscopy (NIRS) via Moxy Monitors to measure muscle oxygen saturation (SmO2) and total hemoglobin, providing direct data on muscle oxidative metabolism. Functional outcomes will be assessed through pressure pain thresholds (algometry) and isometric strength (dynamometry) to determine the effectiveness of each technique in restoring neuromuscular homeostasis.The study will be conducted at the Sierra Varona Physiotherapy Clinic (Toledo) between february and march 2026.
Enrollment
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Inclusion criteria
Professional or Semi-professional athletes (specifically basketball players or endurance athletes) with a minimum of 2 years of competitive experience.
Aged between 18 and 35 years.
Healthy individuals with no current musculoskeletal injuries in the lower limbs.
Regular training frequency of at least 4-5 sessions per week.
Signed informed consent to participate in the study and follow the 6-week crossover protocol.
Commitment to maintain similar nutritional and sleep habits throughout the duration of the study.
Exclusion criteria
Presence of any acute or chronic injury in the gastrocnemius or Achilles tendon in the last 6 months.
Contraindications for specific therapies:
For Shockwave Therapy: Blood clotting disorders or use of anticoagulants.
For TECAR/Diathermy: Metal implants in the lower limbs or pacemakers.
For Cupping: Acute skin infections or dermatological hypersensitivity.
Consumption of performance-enhancing drugs, anti-inflammatory medication (NSAIDs), or stimulants that could affect muscle oxygenation (SmO2) or pain perception.
Recent surgery in the lower extremities (within the last year).
Inability to complete the standardized fatigue protocol or attend all 6 intervention sessions.
Primary purpose
Allocation
Interventional model
Masking
20 participants in 6 patient groups
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Central trial contact
ALBERTO SANCHEZ SIERRA
Data sourced from clinicaltrials.gov
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