Purpose of the Study: This study aims to compare the effects of two different ultrasound-guided percutaneous neuromodulation (PNM) protocols targeting the median nerve on maximal handgrip strength in healthy individuals. The study seeks to enhance scientific understanding of the clinical applications of PNM in improving neuromuscular performance and functional capacity. Benefits of the Study: Contribute to the evidence base supporting the use of PNM in physiotherapy and rehabilitation. Inform future therapeutic protocols aiming to optimize muscle strength and functional recovery. Provide participants with access to a professional evaluation of physical performance and exposure to advanced rehabilitative techniques in a safe and monitored environment. Interventions: Participants will undergo a single session of ultrasound-guided PNM to the median nerve using one of two protocols: Protocol 1 (100 Hz): 5 cycles of 5 seconds stimulation (350 µs pulse width), followed by 55 seconds rest. Protocol 2 (10 Hz): 10 cycles of 10 seconds stimulation (250 µs pulse width), followed by 10 seconds rest. In both protocols, stimulation intensity will be set to the maximum tolerable level that elicits a strong but non-painful muscular contraction. Total treatment duration will be approximately 10 minutes. Measurements: Primary Outcome: Maximal handgrip strength measured using a digital dynamometer before and after the intervention. Secondary Outcomes: Perceived pain during the intervention, assessed with the Numerical Pain Rating Scale (0-10). Sociodemographic data (age, sex, weight, height, BMI). Conclusion: This clinical trial will provide valuable insights into the comparative effectiveness of two PNM protocols for improving muscular performance. By identifying the most effective parameters for PNM application, this research may help optimize rehabilitation strategies and contribute to enhancing patients' functional outcomes in clinical and athletic settings.
Age range
18 Years – 40 Years
Sex
ALL
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Maximum Handgrip Strength
Timeframe: This variable will be measured 2 times: immediately pre-intervention and immediately post-intervention.