Tato stránka byla automaticky přeložena a přesnost překladu není zaručena. Podívejte se prosím na anglická verze pro zdrojový text.

Alterations in Spiking Following Muscle Fatigue in Volleyball Players

1. července 2026 aktualizováno: 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.

Přehled studie

Postavení

Zatím nenabíráme

Podmínky

Typ studie

Pozorovací

Zápis (Odhadovaný)

35

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Studijní místa

      • Taipei, Tchaj-wan, 112
        • National Yang Ming Chiao Tung University
        • Kontakt:
          • National Yang Ming Chiao Tung University
          • Telefonní číslo: (02)2826-7049
          • E-mail: tshuang@nycu.edu.tw

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý

Přijímá zdravé dobrovolníky

Ano

Metoda odběru vzorků

Ukázka pravděpodobnosti

Studijní populace

Healthy recreational volleyball players

Popis

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

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

Kohorty a intervence

Skupina / kohorta
Intervence / Léčba
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.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Degree of the glenohumeral and scapulothoracic joint during spiking
Časové okno: 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
Časové okno: 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
Časové okno: 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)

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Acromio-humeral distance and thickness of supraspinatus tendon thickness during arm elevation
Časové okno: 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
Časové okno: 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)

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. července 2026

Primární dokončení (Odhadovaný)

1. ledna 2027

Dokončení studie (Odhadovaný)

1. ledna 2027

Termíny zápisu do studia

První předloženo

17. prosince 2025

První předloženo, které splnilo kritéria kontroly kvality

1. července 2026

První zveřejněno (Aktuální)

7. července 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

7. července 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

1. července 2026

Naposledy ověřeno

1. listopadu 2025

Více informací

Termíny související s touto studií

Klíčová slova

Další identifikační čísla studie

  • NYCU114118AF

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

3
Předplatit