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Alterations in Spiking Following Muscle Fatigue in Volleyball Players

1 luglio 2026 aggiornato da: National Yang Ming Chiao Tung University

Alterations in Spiking Kinematic, Muscle Activation, and Subacromial Structures Following Muscle Fatigue in Volleyball Players

This study aims (1)to investigate the effects of repetitive functional overhead movements targeting shoulder and scapular muscles on glenohumeral and scapular kinematics and muscle activation during the arm cocking and acceleration of spiking, and changes in subacromial structures in healthy recreational volleyball players; (2) to compare these fatigue-related changes between athletes with good and poor shoulder motor control.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Tipo di studio

Osservativo

Iscrizione (Stimato)

35

Contatti e Sedi

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

Contatto studio

Luoghi di studio

      • Taipei, Taiwan, 112
        • National Yang Ming Chiao Tung University
        • Contatto:
          • National Yang Ming Chiao Tung University
          • Numero di telefono: (02)2826-7049
          • Email: tshuang@nycu.edu.tw

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

Metodo di campionamento

Campione di probabilità

Popolazione di studio

Healthy recreational volleyball players

Descrizione

Inclusion Criteria:

  • Between 18 and 35 years old
  • At least 2 consecutive years of volleyball experience
  • Involved in volleyball practice or game for at least 4 hours per week
  • Able to perform a cross-body spike with 3-step

Exclusion Criteria:

  • A history of major shoulder or spinal injury or surgery
  • Experiencing shoulder pain (VAS ≥ 3/10) in the last 6 months

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

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Poor shoulder motor control
During shoulder medial rotation up to 60° in supine position, the scapula forward tilts or elevation occurs, difficulties in breathing, performing difficulties, unable to perform 60° medial rotation, glenohumeral anterior translation, fatigue, the need of external feedback and external support.

The subject performed upper extremity D2 diagonal exercise with Thera-band at kneeling position to simulate the arm movement of a volleyball spike. The movement is paced by a metronome at one beat per second, with one movement per beat. If participants could not keep up or become too fatigued, they are allowed to rest for 15 seconds before continuing.

The subject was defined as fatigued, and the fatigue activity was stopped, only when all three of the following cumulative conditions were met:

  1. Until the number of repetitions in that set was less than 50% of the repetitions performed in the first set.
  2. Using the Rating of Perceived Exertion (RPE) on a 6-20 scale, until the subject's RPE was greater than or equal to 15.
  3. If this maximum strength showed a decrease of 25% or more compared to the maximum strength measured before the fatigue activity.
Good shoulder motor control
During shoulder medial rotation up to 60° in supine position, no scapula and glenohumeral compensation, easy to breathing and perform 60° medial rotation without external feedback and external support.

The subject performed upper extremity D2 diagonal exercise with Thera-band at kneeling position to simulate the arm movement of a volleyball spike. The movement is paced by a metronome at one beat per second, with one movement per beat. If participants could not keep up or become too fatigued, they are allowed to rest for 15 seconds before continuing.

The subject was defined as fatigued, and the fatigue activity was stopped, only when all three of the following cumulative conditions were met:

  1. Until the number of repetitions in that set was less than 50% of the repetitions performed in the first set.
  2. Using the Rating of Perceived Exertion (RPE) on a 6-20 scale, until the subject's RPE was greater than or equal to 15.
  3. If this maximum strength showed a decrease of 25% or more compared to the maximum strength measured before the fatigue activity.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Degree of the glenohumeral and scapulothoracic joint during spiking
Lasso di tempo: Baseline, immediately post-intervention (Day 1)

The kinematics is assessed using an electromagnetic motion tracking system (VIPERTM, Polhemus, USA) to measure the glenohumeral elevation, horizontal abduction/adduction, internal/external rotation, and scapulothoracic retraction/protraction, upward/downward rotation, anterior/posterior tilt during spiking movement. During the test, participants performed 3 times of cross-body spikes, with 15 seconds of rest between each trial.

Data were collected at the end of the arm cocking (maximal shoulder horizontal abduction) and at ball-contact (maximal footswitch signal), and reported as mean values for each trial. (unit of measure: degree, °)

Baseline, immediately post-intervention (Day 1)
Activation amplitude of the glenohumeral and periscapular muscles
Lasso di tempo: Baseline, immediately post-intervention (Day 1)

The muscle activation amplitude of the serratus anterior, upper trapezius, lower trapezius, middle deltoid, infraspinatus, and pectoralis major during spiking movement. During the test, participants performed 3 times of cross-body spikes, with 15 seconds of rest between each trial.

Data were collected in the arm cocking phase (from minimal shoulder elevation to the shoulder maximal horizontal abduction) and the acceleration phase (from maximal shoulder horizontal abduction to the ball-contact), and reported as mean values for each trial. (unit of measure: percentage, %)

Baseline, immediately post-intervention (Day 1)
Mean power frequency of the glenohumeral and periscapular muscles
Lasso di tempo: Baseline, immediately post-intervention (Day 1)

The mean power frequency of the serratus anterior, upper trapezius, lower trapezius, middle deltoid, infraspinatus, and pectoralis major during spiking movement. During the test, participants performed 3 times of cross-body spikes, with 15 seconds of rest between each trial.

Data were collected in the arm cocking phase (from minimal shoulder elevation to the shoulder maximal horizontal abduction) and the acceleration phase (from maximal shoulder horizontal abduction to the ball-contact), and reported as mean values for each trial. (unit of measure: hertz, Hz)

Baseline, immediately post-intervention (Day 1)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Acromio-humeral distance and thickness of supraspinatus tendon thickness during arm elevation
Lasso di tempo: Baseline, immediately post-intervention (Day 1)

The subacromial structures is assessed using a diagnostic ultrasound system (SONIMAGE MX1 Ver. 1.10, Konica Minolta, Inc., Tokyo, Japan) to measure the acromio-humeral distance (AHD, from the lateral inferior edge of the acromion perpendicular to the humerus), supraspinatus tendon thickness (SST, from the subacromial-subdeltoid bursa perpendicular to the humerus), occupation ratio (OR, dividing SST by AHD). During the dynamic evaluation, participants performed 3 times of arm elevation to 90° and returning to the neutral position at scapular plane. During the static evaluation, participants performed 3 times of arm elevation to 60° at scapular plane.

Data of dynamic evaluation is collected at 0° elevation and at the greater tuberosity of the humerus is aligned under the lateral inferior edge of the acromion. Data of static evaluation is collected at 0° elevation and 60° elevation. Data reported as mean values for each trial. (unit of measure: millimeter, mm)

Baseline, immediately post-intervention (Day 1)
Degree of shoulder elevation at greater tuberosity-acromion alignment during arm elevation
Lasso di tempo: Baseline, immediately post-intervention (Day 1)
The shoulder elevation angle is measured using a application software (Measure, Apple Inc., USA) at at greater tuberosity of humerus under Lateral inferior edge of the acromion, which assess diagnostic ultrasound system (SONIMAGE MX1 Ver. 1.10, Konica Minolta, Inc., Tokyo, Japan), and reported as mean values for each trial. (unit of measure: degree, °).
Baseline, immediately post-intervention (Day 1)

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 (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 gennaio 2027

Completamento dello studio (Stimato)

1 gennaio 2027

Date di iscrizione allo studio

Primo inviato

17 dicembre 2025

Primo inviato che soddisfa i criteri di controllo qualità

1 luglio 2026

Primo Inserito (Effettivo)

7 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

7 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 luglio 2026

Ultimo verificato

1 novembre 2025

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • NYCU114118AF

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 .

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