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NCT Number: NCT07387276

"Recovery Techniques on Pain, Force and Muscle Oxygenation in Athletes: A Crossover Trial"

The goal of this clinical trial is to evaluate the impact of various passive post-exercise 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 following high-intensity effort?

Which specific technique is most effective in reducing perceived pain, measured by the pressure pain threshold, and restoring muscle strength?

Researchers will compare six different therapeutic interventions-Transfer of Energy Capacitive and Resistive therapy, manual massage, intermittent negative pressure therapy, extracorporeal shockwave therapy, percussion therapy, and pneumatic pressotherapy-to determine which provides a 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 near-infrared spectroscopy to assess muscle oxygen saturation, tissue thermography, algometry, and dynamometry.

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Key information

About this study

This project is designed as a randomized, double-blind (outcome assessor and statistician), crossover clinical trial. The study aims to address the critical need for evidence-based recovery strategies in high-demand sports such as basketball, where muscle overload is a primary risk factor for injury.The investigation will focus on the immediate physiological and functional effects of six widely utilized physiotherapy modalities:Capacitive and Resistive Energy Transfer (TECAR) Therapy: Utilized to improve tissue perfusion and modulate inflammatory responses through deep endogenous thermotherapy.Percussive Massage Therapy: Applied via mechanical vibration to reduce muscular stiffness and enhance explosive force restoration.Extracorporeal Shockwave Therapy (ESWT): Evaluated for its capacity to enhance muscular microcirculation and accelerate immediate tissue metabolic activity.Intermittent Pneumatic Compression (Pressotherapy): Targeted at reducing perceived pain and the sensation of limb heaviness through mechanical fluid drainage.Intermittent Negative Pressure Therapy (Vacuum Therapy): Investigated for its role in localized blood flow enhancement and pain modulation.Manual Sports Massage: Defined as the traditional manual intervention for reducing perceived muscle soreness and improving soft tissue flexibility.Physiological monitoring will be conducted using Near-Infrared Spectroscopy (NIRS) to measure muscle oxygen saturation ($SmO_2$) and total hemoglobin, providing direct data on muscle oxidative metabolism. Functional outcomes will be assessed through pressure pain thresholds (PPT) via algometry and maximal isometric strength via dynamometry to determine the effectiveness of each technique in restoring neuromuscular homeostasis.The study will be conducted at the Sierra Varona Physiotherapy Clinic (Toledo, Spain) between February and March 2026..

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Extracorporeal Shockwave Therapy (ESWT)

Device

Application of acoustic pulses to the gastrocnemius muscle to modulate tissue mechanotransduction and improve local microcirculation.

Massage Gun

Device

Mechanical vibration applied to the calf muscles to promote myofascial release and neuromuscular recovery through high-frequency percussion.

TECAR Therapy

Device

Application of high-frequency electromagnetic energy (diathermy) to the lower limb to induce deep endogenous heat and accelerate metabolic waste removal.

Manual massage

Other

Systematic manipulation of soft tissues using manual techniques (effleurage and petrissage) focused on reducing muscle tension and perceived soreness.

cupping

Device

Controlled suction therapy applied to the gastrocnemius to create space between fascial layers and stimulate lymphatic and venous drainage.

Pressotherapy

Device

External pneumatic compression through a sequential inflation system to facilitate venous return and reduce lower limb edema post-effort.

Primary outcomes

  1. Muscle Oxygen Saturation (SmO2)

    Time frame: immediately post-effort (fatigue), and immediately post-intervention (recovery).

    Measured using Moxy Monitor (Near-Infrared Spectroscopy - NIRS). It evaluates the percentage of hemoglobin/myoglobin oxygenated in the gastrocnemius muscle.

  2. Pressure Pain Threshold (PPT)

    Time frame: immediately post-effort (fatigue), and immediately post-intervention (recovery).

    Measured using a digital pressure algometer. It quantifies the minimum pressure (in kg/cm²) at which a participant perceives the stimulus as painful in the gastrocnemius.

  3. Maximum Isometric Muscle Strength

    Time frame: immediately post-effort (fatigue), and immediately post-intervention (recovery).

    Measured using a handheld dynamometer. It evaluates the peak force (in Newtons) during a maximum voluntary isometric contraction of the calf muscles.

Secondary outcomes

  1. Muscle Surface Temperature

    Time frame: immediately post-effort (fatigue), and immediately post-intervention (recovery).

    Measured using a digital infrared thermography camera. It assesses the changes in skin surface temperature over the gastrocnemius muscle area, reflecting changes in local blood flow.

  2. Participant Satisfaction and Perceived Recovery

    Time frame: 5 minutes after each recovery intervention.

    Measured using a Visual Analog Scale (VAS) and a customized survey (Likert scale 1-5). Participants rate which recovery modality felt better and their perceived level of muscle readiness for a new effort.

Study contacts

Contact information is provided by the study sponsor or research team.

ALBERTO SANCHEZ SIERRA

CONTACT

[email protected]

608801238

Sponsors and collaborators

Lead sponsor

Sierra Varona SL

Other

Registry information

Official study title

"Effects of Multiple Muscle Recovery Techniques on Pain, Force, Temperature, and Muscle Oxygenation in Professional Athletes: A Randomized Crossover Trial"

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 4, 2026
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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