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Effect of the Ultrasound-guided Percutaneous Neuromodulation on the Mean Velocity in Crossfit Practitioners.

8 juli 2026 bijgewerkt door: Paco Navarro Pastor, CEU San Pablo University

Effect of Ultrasound-guided Percutaneous Neuromodulation of the Transversus Abdominis on the Force-Velocity Profile During the Squat Performance in Crossfit Practitioners.

This randomized controlled blinded clinical trial aims to evaluate the effect of ultrasound-guided percutaneous neuromodulation (US-guided PNM) targeting the innervation of the transversus abdominis muscle on squat performance in CrossFit practitioners.

The transversus abdominis is a deep trunk muscle that contributes to lumbopelvic stability and force transmission during functional and athletic movements. Previous research suggests that improving neuromuscular activation of the trunk musculature may enhance movement efficiency and performance during resistance exercises. Ultrasound-guided percutaneous neuromodulation is a minimally invasive technique that applies electrical stimulation through a needle placed close to a peripheral nerve under ultrasound guidance, with the aim of modulating neuromuscular function.

Healthy male and female CrossFit practitioners aged 18 to 60 years, with at least one year of training experience, will participate in the study. Participants will undergo an initial ultrasound assessment of transversus abdominis activation to classify and distribute the sample into groups. In a second session, mean velocity, mean propulsive velocity, and velocity loss during squat performance will be assessed using a linear velocity transducer. Participants will perform 3 sets of 2 repetitions of the squat exercise at 80% of their one-repetition maximum (1RM).

Following baseline assessment, participants will be randomly assigned to either an experimental group receiving ultrasound-guided percutaneous neuromodulation of the iliohypogastric and ilioinguinal nerves, or a sham group receiving needle insertion without electrical stimulation. The intervention will consist of a TENS-type current applied at 10 Hz for 10 cycles of 10 seconds. Squat performance variables will be reassessed immediately after the intervention.

The purpose of this study is to determine whether US-guided percutaneous neuromodulation can acutely improve squat performance in trained CrossFit practitioners. The study hypothesis is that participants receiving active neuromodulation will demonstrate greater improvements in squat execution velocity and lower velocity loss compared with participants receiving the sham intervention.

Studie Overzicht

Toestand

Werving

Conditie

Interventie / Behandeling

Gedetailleerde beschrijving

CrossFit training requires the integration of strength, power, trunk stability, and efficient force transmission during complex multi-joint movements. The back squat is one of the most frequently used exercises in CrossFit and is commonly applied to assess lower-limb performance through force-velocity profiling. Variables such as mean velocity, mean propulsive velocity, and velocity loss between sets provide relevant information regarding neuromuscular performance and fatigue resistance.

The transversus abdominis is a deep abdominal muscle involved in trunk stabilization and lumbopelvic control. Adequate activation of this muscle may contribute to improved force transmission between the lower and upper extremities during strength exercises. Ultrasound-guided percutaneous neuromodulation (UGPNM) is an invasive physiotherapy technique that delivers electrical stimulation through a needle placed near a peripheral nerve under ultrasound guidance. This intervention has been proposed as a method to modulate neuromuscular function and potentially enhance motor performance.

Despite the increasing use of ultrasound-guided percutaneous neuromodulation in clinical and sports settings, evidence regarding its immediate effects on sport performance variables remains limited. In particular, the influence of neuromodulation targeting the innervation of the transversus abdominis on force-velocity profile characteristics during the squat has not been thoroughly investigated.

The objective of this randomized controlled trial is to evaluate the immediate effects of ultrasound-guided percutaneous neuromodulation of the nerves supplying the transversus abdominis on mean velocity during the back squat in CrossFit practitioners. Secondary outcomes include mean propulsive velocity, fatigue resistance assessed through velocity loss between sets, perceived exertion, and potential differences in response according to baseline transversus abdominis activation capacity.

A total of 42 healthy CrossFit practitioners, both male and female, aged 18 to 60 years with at least one year of training experience, will be recruited. During baseline assessment, participants will undergo ultrasound evaluation of the transversus abdominis muscle at rest and during voluntary contraction. Muscle thickness will be measured in both conditions, and the percentage of activation will be calculated based on the relative change in thickness. Participants will then be classified into higher and lower activation subgroups according to the median value of transversus abdominis activation.

Following this classification, participants will be randomly allocated to either the experimental or sham group using block randomization performed with R statistical software, ensuring balanced distribution of activation levels between groups.

A blinded randomized controlled design with third-party outcome assessment will be used. Outcome assessments will be performed by a blinded evaluator responsible for ultrasound measurements of transversus abdominis thickness and for collecting squat performance variables obtained via a linear velocity transducer. The evaluator will not be involved in the randomization process and will remain unaware of group allocation throughout the study.

A separate clinician, not involved in outcome assessment, will administer either the active ultrasound-guided percutaneous neuromodulation intervention or the sham procedure. Participants will remain blinded to treatment allocation throughout the study.

The baseline performance assessment will include squat testing using a linear velocity transducer. Participants will perform three sets of two repetitions at 80% of their individual one-repetition maximum (1RM), following a standardized warm-up. Mean velocity, mean propulsive velocity, velocity loss, and rating of perceived exertion will be recorded.

The experimental intervention will consist of ultrasound-guided percutaneous neuromodulation applied to the iliohypogastric and ilioinguinal nerves using electrical stimulation at 10 Hz in 10-second cycles. The sham condition will involve identical needle insertion without electrical stimulation. Immediately after the intervention, all performance variables will be reassessed under identical testing conditions.

This study aims to determine whether ultrasound-guided percutaneous neuromodulation can produce immediate improvements in squat performance variables and whether baseline transversus abdominis activation capacity influences the response to the intervention.

Studietype

Ingrijpend

Inschrijving (Geschat)

42

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

  • Spanje
    • Murcia
      • Murcia, Murcia, Spanje, 30007
        • Werving
        • Fisiosport premium SL
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion Criteria:

  • Age between 18 and 60 years
  • At least 1 year of CrossFit training experience
  • Training frequency between 2 and 6 sessions per week

Exclusion Criteria:

  • Belonephobia (fear of needles)
  • Presence of cardiac conditions or implanted cardiac devices (e.g., pacemaker)
  • Pregnancy
  • Active oncological process
  • Skin conditions or lesions in the intervention area
  • Neurological or neurosensory disorders
  • Epilepsy
  • Current febrile condition
  • Recent use of antibiotics
  • Treatment with anticoagulant medication
  • Use of medications that may affect physical performance
  • Autoimmune diseases or use of immunosuppressive therapy
  • Active lumbar or abdominal pathology
  • Recent lumbar surgery or operations related to the intervention area
  • Active musculoskeletal injury or pain affecting squat technique or -performance
  • Undiagnosed pain affecting execution of the sporting movement.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ander
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Dubbele

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: ultrasound-guided percutaneous neuromodulation
The patients will receive ultrasound-guided percutaneous neuromodulation of the iliohypogastric and ilioinguinal nerves using electrical stimulation at 10 Hz in 10-second cycles.
Ander: ultrasound-guided percutaneous neuromodulation
The intervention will be applied using ultrasound-guided percutaneous neuromodulation of the iliohypogastric and ilioinguinal nerves. The procedure will be performed under ultrasound guidance using a sterile percutaneous needle. In the experimental group, electrical stimulation will be delivered through the needle at a frequency of 10 Hz in 10-second cycles. Stimulation intensity will be adjusted according to participant tolerance, without exceeding the pain threshold.
Sham-vergelijker: Ultrasound-guided percutaneous neuromodulation (sham)
The patients will receive a sham ultrasound-guided percutaneous neuromodulation procedure involving identical needle insertion under ultrasound guidance without electrical stimulation
Ander: ultrasound-guided percutaneous neuromodulation (sham)
The sham intervention consists of an ultrasound-guided percutaneous needle insertion performed in the same anatomical region as the experimental procedure (iliohypogastric and ilioinguinal nerves), using identical positioning and procedural setup. No electrical stimulation is delivered through the needle at any point during the procedure. The duration and handling of the procedure are matched to the experimental condition to ensure participant blinding.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Mean Velocity during Back Squat (Linear Velocity Transducer)
Tijdsspanne: Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).
Mean velocity will be measured using a linear position transducer attached to the barbell during the back squat exercise. This device records bar displacement over time and allows calculation of bar velocity during the concentric phase of each repetition. The mean velocity of each repetition will be recorded, and the average across repetitions and sets will be used for analysis.
Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Mean Propulsive Velocity during Back Squat (Linear Velocity Transducer)
Tijdsspanne: Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).
Mean propulsive velocity will be measured using a linear position transducer attached to the barbell during the back squat exercise. Mean propulsive velocity corresponds to the average bar velocity during the propulsive phase of the concentric movement, from the start of the upward movement until bar acceleration falls below gravitational acceleration. The average value across repetitions and sets will be used for analysis.
Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).
Velocity Loss Between Sets during Back Squat (Linear Velocity Transducer)
Tijdsspanne: Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).
Velocity loss between sets will be calculated from the mean velocity recorded by the linear position transducer during the back squat exercise. This variable will be expressed as the percentage reduction in movement velocity between sets and will be used as an indicator of fatigue resistance.
Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).
Rating of Perceived Exertion (RPE)
Tijdsspanne: Baseline assessment (pre-intervention), immediately after the intervention (post-intervention, same session), 1 week after the intervention, and 2 weeks after the intervention.
Perceived exertion during the back squat exercise will be assessed using a rating of perceived exertion (RPE) scale. Participants will rate the perceived intensity of the exercise after completing the squat protocol. Higher scores indicate greater perceived effort.
Baseline assessment (pre-intervention), immediately after the intervention (post-intervention, same session), 1 week after the intervention, and 2 weeks after the intervention.
Activation of the transverse abdominal muscle
Tijdsspanne: Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).
The investigators will measure the resting and activation thicknesses and will calculate the activation ratio.
Baseline assessment (pre-intervention) and immediately after the intervention (post-intervention, same session).

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

CEU San Pablo University

Onderzoekers

  • Hoofdonderzoeker: Francisco N Navarro Pastor, Physiotherapist, CEU San Pablo University

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

8 juli 2026

Primaire voltooiing (Geschat)

1 oktober 2026

Studie voltooiing (Geschat)

1 november 2026

Studieregistratiedata

Eerst ingediend

29 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

29 juni 2026

Eerst geplaatst (Werkelijk)

6 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

10 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

8 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • CdEi94

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

Anonymized study data will be made available to other researchers upon reasonable request and following consultation with the principal investigator

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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