Effects of Percutaneous Neuromodulation on Vertical Jump
Effects of Ultrasound-Guided Percutaneous Neuromodulation of the Femoral Nerve on Vertical Jump Performance.
1 other identifier
interventional
29
1 country
1
Brief Summary
Vertical jump performance is a determinant factor in physical performance, both in sports and in daily life and work activities. The muscular power of the lower limbs and the ability to generate explosive strength directly influence vertical jump performance and athletic success. For this reason, the vertical jump is widely used as a field test to evaluate performance capacity. Different strategies have been used to improve vertical jump performance, such as plyometric training (PT) and electrostimulation (EMS). PT consists of stretch-shortening cycle movements that involve high-intensity eccentric contractions followed by rapid and powerful concentric actions. EMS applies electrical current over muscles or peripheral nerves to generate involuntary muscle contractions. Both methods have shown significant effects in improving vertical jump height. In recent years, new therapeutic techniques have emerged in physiotherapy to improve neuromuscular recruitment and functionality, such as ultrasound-guided percutaneous neuromodulation (PNM-e). This technique consists of the electrical stimulation of a peripheral nerve or a motor point through a needle under ultrasound guidance, for therapeutic purposes. Evidence suggests that PNM-e can improve pain, functionality, balance, and muscle endurance, and increase muscle strength immediately after application. Specifically, low-frequency PNM-e applied to the femoral nerve has been shown to increase maximal quadriceps strength and vertical jump height in athletes. The femoral nerve plays a key role in quadriceps activation, a muscle group essential for knee extension and hip flexion, functions that are indispensable for both daily and sports activities. However, the specific effects of femoral nerve PNM-e on power and biomechanics of the vertical jump have not been sufficiently explored. Therefore, the main objective of this pilot study was to evaluate the effects of ultrasound-guided percutaneous neuromodulation of the femoral nerve on vertical jump performance. The secondary objective was to compare the effects of isolated plyometric training versus its combination with PNM-e to determine whether the combined approach offers additional benefits on jump performance. A randomized experimental study was carried out with healthy athletes who regularly practice sports. Participants were randomly assigned to a control group (two plyometric training sessions) or to an experimental group (two plyometric training + PNM-e interventions sessions); in both cases the sessions were separated by 7 days. Vertical jump performance was measured twice using the countermovement jump (CMJ) test (before the first session and after the second one). It is expected that ultrasound-guided percutaneous neuromodulation of the femoral nerve, combined with plyometric training, will produce greater improvements in jump performance due to enhanced quadriceps activation and neuromuscular efficiency.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 8, 2025
CompletedFirst Submitted
Initial submission to the registry
April 6, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
April 13, 2026
October 1, 2025
11 months
April 6, 2026
April 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Vertical Jump Height
Vertical jump height will be assessed using the MyJump2 app. This tool allows for precise measurement of jump height through video recording and frame-by-frame analysis. Each participant will perform ten maximum jumps in each measurement, and all results will be recorded. The evaluation will be carried out under standardized conditions, with participants dressed in athletic wear and after a warm-up.
Baseline (pre-intervention) and post-intervention (after 1 week).
Secondary Outcomes (4)
Flight Time
Baseline (pre-intervention) and post-intervention (after 1 week).
Force
Baseline (pre-intervention) and post-intervention (after 1 week).
Movement Velocity
Baseline (pre-intervention) and post-intervention (after 1 week).
Power
Baseline (pre-intervention) and post-intervention (after 1 week).
Study Arms (2)
Plyometric Training
ACTIVE COMPARATORFemoral nerve NMP + Plyometric training
EXPERIMENTALInterventions
The plyometric training program used was the one described by Sankey et al. as an effective exercise program for improving vertical jump: * 2 sets of 10 tuck jumps. * 2 sets of 10 alternating leg bounds. * 2 sets of 15 two-footed bench hops. * 2 sets of 20 rim jumps. The rest time between sets was 60 seconds.
Bilateral application of an asymmetric biphasic current to the femoral nerve with a frequency of 10 Hz and a pulse width of 240 µs. The intensity of the current was increased until a visible but painless motor response was achieved, using the 10-10-10 protocol (10 seconds of stimulation - 10 seconds of rest - 10 repetitions) described by MVClinic Institute. The current was applied using Physio Invasiva 2.0 ®, and Agupunt APS® needles were used, the length of which depended on the patient's anatomy, taking as a safety reference the measurement of the distance from the skin to the target tissue, estimating the size between 0.30 x 40 and 0.30 x 50 mm. Before needle insertion, the skin was cleansed with isopropyl alcohol and chlorhexidine, a clean skin antiseptic. After locating the femoral nerve in the femoral triangle using a General Electrics LOGIQ S7 ultrasound system, the needle was introduced using a long-axis approach, at a 45° angle to the skin, until it reached the epineurium of t
Eligibility Criteria
You may qualify if:
- Practice at least 6 hours of physical activity a week.
You may not qualify if:
- Serious illnesses
- Cardiovascular pathologies
- Physical injuries that prevented them from participating in sports in the three months prior to the start of the study
- Any absolute contraindication to invasive physical therapy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centro de Fisioterapia FyS
Narón, A Coruña, 15570, Spain
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Francisco Minaya Muñoz, Doctor
CEU San Pablo University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Student at CEU San Pablo University
Study Record Dates
First Submitted
April 6, 2026
First Posted
April 13, 2026
Study Start
July 8, 2025
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
April 13, 2026
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to the nature of the study as a university master's project and the lack of a formal data sharing plan.