Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Acute Effects of Neuroathletic Training-Integrated Resistance Training in Collegiate Athletes (NAT-RT)

24 agosto 2026 aggiornato da: Ankara Yildirim Beyazıt University

Neural Priming Before Performance: Acute Effects of Neuroathletic Training-Integrated Resistance Training Versus Conventional Resistance Training on Sprint Acceleration, Jump Performance, Eccentric Hamstring Strength, Flexibility, and Bilateral Hamstring Symmetry in Collegiate Athletes

This study investigated the acute and short-term effects of neuroathletic training (NAT)-integrated resistance training compared with conventional resistance training on physical and neuromuscular performance in collegiate athletes. Fifty-eight collegiate athletes completed two experimental resistance training sessions separated by one week. The conventional resistance training condition was performed first, followed one week later by a NAT-integrated resistance training condition.

Both sessions included the same lower-extremity resistance exercises, training volume, intensity, exercise order, and rest intervals. During the NAT-integrated condition, visual, vestibular, gaze-stabilization, and proprioceptive drills were incorporated before selected resistance sets and during rest intervals. Sprint acceleration, bilateral and unilateral jump performance, eccentric hamstring strength, bilateral hamstring maximum difference, and sit-and-reach flexibility were assessed before training, immediately after training, 15 minutes after training, and 30 minutes after training.

Panoramica dello studio

Descrizione dettagliata

Neuroathletic training is an emerging training approach that incorporates visual, vestibular, proprioceptive, and sensorimotor exercises with the aim of improving the quality of sensory input and motor readiness. The purpose of the present study was to determine whether integrating brief neuroathletic training drills into a conventional lower-extremity resistance training session could influence acute and short-term physical performance responses in trained collegiate athletes.

The study used a non-randomized, fixed-order, within-participant repeated-measures intervention design. Fifty-eight collegiate athletes completed two experimental sessions separated by one week. During the first experimental session, participants completed conventional lower-extremity resistance training. During the second session, participants completed the same resistance training program combined with neuroathletic training drills. Therefore, each participant served as their own control.

The resistance training protocol consisted of leg press, Romanian deadlift, leg extension, seated leg curl, dumbbell step-up, and Copenhagen exercise. Training volume, intensity, exercise order, and rest intervals were matched between conditions. During the conventional condition, rest intervals consisted of passive rest. During the NAT-integrated condition, participants completed a 6-8-minute pre-session neuroathletic activation block followed by brief neuroathletic primers before selected resistance sets and during rest intervals. These drills included binocular and monocular convergence-divergence tasks, unilateral eye occlusion, gaze stabilization, vertical and horizontal vestibular stimulation, head-position variations, and proprioceptive awareness exercises.

Performance assessments were conducted before training (T0), immediately after training (T1), 15 minutes after training (T2), and 30 minutes after training (T3) during each experimental condition. Outcome measures included 5-meter sprint acceleration, bilateral countermovement jump performance, right- and left-leg unilateral jump performance, eccentric hamstring strength assessed using the IVMES H-Bord during the Nordic hamstring exercise, bilateral maximum difference between hamstring strength outputs, and sit-and-reach flexibility.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

58

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

  • Were collegiate athletes participating in organized sport training.
  • Had participated in regular sport-specific training for at least one year.
  • Had previous experience with lower-extremity resistance training.
  • Had previous experience with the exercises used in the study, including leg press, Romanian deadlift, leg extension, seated leg curl, dumbbell step-up, and Copenhagen exercise.
  • Were familiar with maximal or near-maximal sprinting, jumping, and lower-limb strength testing.
  • Were able to complete 5-meter sprint testing, bilateral and unilateral jump testing, Nordic hamstring testing, sit-and-reach flexibility testing, and the resistance training protocols.
  • Were able to perform maximal or near-maximal lower-limb tasks without pain or movement restriction.
  • Agreed to attend both experimental sessions and all measurement time points.

Exclusion Criteria:

  • Had an acute lower-extremity musculoskeletal injury during the previous three months.
  • Had a hamstring strain, quadriceps strain, groin injury, ankle sprain, knee injury, hip injury, or low back pain limiting sport participation during the previous three months.
  • Had undergone lower-extremity surgery during the previous 12 months.
  • Experienced current pain during sprinting, jumping, Nordic hamstring testing, flexibility testing, or resistance exercise.
  • Had a neurological disorder.
  • Had diagnosed vestibular dysfunction.
  • Had recurrent vertigo or unexplained dizziness.
  • Had severe motion sensitivity.
  • Had a balance disturbance.
  • Had uncorrected visual impairment.
  • Had diplopia or severe visual tracking difficulties.
  • Had any condition preventing safe completion of eye-occlusion or gaze-stabilization exercises.
  • Had experienced concussion within the previous six months.
  • Had persistent post-concussion symptoms.
  • Had cardiovascular, respiratory, metabolic, or systemic disease limiting high-intensity exercise.
  • Used medication known to influence balance, alertness, reaction time, exercise tolerance, or neuromuscular performance.
  • Failed to comply with pre-test instructions.
  • Failed to attend both experimental sessions.
  • Had incomplete data at any measurement time point.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Fixed-Order Conventional and NAT-Integrated Resistance Training
All enrolled athletes completed two experimental sessions separated by one week. During the first session, participants completed conventional lower-extremity resistance training. During the second session, participants completed the same resistance training program with additional neuroathletic visual, vestibular, gaze-stabilization, and proprioceptive drills performed before selected sets and during rest intervals.

Participants completed a standardized lower-extremity resistance training session consisting of six exercises: leg press, Romanian deadlift, leg extension, seated leg curl, dumbbell step-up, and Copenhagen exercise.

Leg press: 4 sets of 8-10 repetitions at approximately RPE 7-8, with 90 seconds rest.

Romanian deadlift: 4 sets of 6-8 repetitions with a controlled 4-second eccentric phase and 90 seconds rest.

Leg extension: 4 sets of 8-12 repetitions with an explosive concentric phase and 75-90 seconds rest.

Seated leg curl: 4 sets of 8-10 repetitions with a 4-5-second eccentric phase and 90 seconds rest.

Dumbbell step-up: 3 sets of 6-8 repetitions per leg with 90 seconds rest. Copenhagen exercise: 3 sets of 20-30 seconds per side with 60-90 seconds rest. Rest intervals consisted of passive rest only. No visual, vestibular, proprioceptive, gaze-stabilization, unilateral eye-occlusion, saccular, or utricular drills were performed.

Participants completed the same lower-extremity resistance training protocol used in the conventional condition. The NAT-integrated condition additionally included a 6-8-minute pre-session neuroathletic activation block and brief neuroathletic primers before selected resistance sets and during rest intervals.

The neuroathletic components included binocular convergence-divergence exercises, monocular convergence-divergence with unilateral eye occlusion, vertical vestibular/saccular stimulation, horizontal or linear vestibular stimulation, gaze stabilization, head-position variation, and proprioceptive awareness tasks.

The purpose of these drills was to provide acute neural priming through visual, vestibular, oculomotor, proprioceptive, and sensorimotor stimulation while maintaining the same resistance training volume and intensity as the conventional condition.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Bilateral Hamstring Maximum Difference (MD)
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.

Maximum between-limb difference in eccentric hamstring strength. MD was calculated as:

MD (%) = |Right limb value - Left limb value| / higher limb value × 100 Lower values indicate greater bilateral symmetry.

Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Eccentric Hamstring Strength
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each of the two experimental sessions separated by one week.
Eccentric hamstring strength was assessed using the IVMES H-Bord during the Nordic hamstring exercise. Peak eccentric force was recorded separately for the left and right limbs (Max Left and Max Right), together with device-derived left- and right-side strength outputs (T Left and T Right).
Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each of the two experimental sessions separated by one week.
Sit-and-Reach Flexibility
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Hamstring-related posterior chain flexibility assessed using the standard sit-and-reach test. Distance was recorded in centimeters, with higher values representing greater flexibility.
Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
5-Meter Sprint Acceleration
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Short-distance acceleration performance measured using an electronic photocell timing gate system. Sprint time was recorded in seconds. Lower values indicate better acceleration performance.
Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Bilateral Jump Performance
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Maximal bilateral countermovement jump performance recorded in centimeters. Higher values indicate greater lower-limb explosive performance.
Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Right-Leg Unilateral Jump
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Maximum single-leg jump performance of the right limb recorded in centimeters. The best valid trial was used.
Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Left-Leg Unilateral Jump
Lasso di tempo: Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.
Maximum single-leg jump performance of the left limb recorded in centimeters. The best valid trial was used.
Baseline, immediately post-training, 15 minutes post-training, and 30 minutes post-training during each experimental session.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

10 marzo 2026

Completamento primario (Effettivo)

10 aprile 2026

Completamento dello studio (Effettivo)

10 giugno 2026

Date di iscrizione allo studio

Primo inviato

20 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

20 agosto 2026

Primo Inserito (Effettivo)

24 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

25 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

24 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

De-identified individual participant data will be available from the corresponding author upon reasonable request, subject to applicable ethical and institutional requirements.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Sottoscrivi