Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Acute Effects of Shoulder Dynamic Taping in Competitive Volleyball Players

30 octobre 2026 mis à jour par: Serdar Demirci, Balikesir University

Acute Effects of Shoulder Dynamic Taping on Serve Velocity, Shoulder Rotator Muscle Strength, and Functional Throwing Performance in Competitive Volleyball Players: A Sham-Controlled Randomized Trial

This randomized, sham-controlled study investigated the acute effects of shoulder Dynamic Tape on serve velocity, isometric shoulder rotator muscle strength, functional throwing performance, and athlete satisfaction in competitive volleyball players. Thirty athletes aged 18-35 years were randomly assigned to a Dynamic Tape group (n = 15) or a sham taping group (n = 15). In both groups, serve velocity, shoulder internal and external rotation strength, and functional throwing performance were assessed under taped and untaped conditions. The order of the assessment conditions was randomized to minimize order effects. Assessments under the taped condition were performed 45 minutes after tape application. Athlete satisfaction was evaluated following taping.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

30

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Altıeylul
      • Balıkesir, Altıeylul, Turquie (Türkiye), 10145
        • Balikesir University

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 35 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Femelle

La description

Inclusion Criteria:

  • Aged between 18 and 35 years.
  • Willing to participate in the study and providing written informed consent.
  • Playing competitively for a volleyball club participating in the Turkish Volleyball League.

Exclusion Criteria:

  • History of shoulder surgery within the previous 12 months.
  • Shoulder injury within the previous 3 months.
  • Presence of any systemic or neurological disorder.
  • Known allergy to the taping material.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Dynamic Tape

Fifteen competitive volleyball players were assigned to the Dynamic Tape group. Dynamic Tape was applied to the dominant shoulder using a spiral technique designed to provide mechanical support to the shoulder complex. Serve velocity, isometric shoulder internal and external rotation strength, and functional throwing performance were assessed under taped and untaped conditions. Assessments in the taped condition were performed 45 minutes after tape application.

Dynamic Tape was applied to the dominant shoulder with the glenohumeral joint internally rotated and the hand resting on the ipsilateral hip. The tape was anchored to the distal lateral humerus and applied proximally in a spiral pattern at approximately 45°, passing posterior to the glenohumeral joint. It was then directed anteriorly across the shoulder onto the chest to provide mechanical support. The initial and final 3-4 cm of the tape were applied without tension.

Autres noms:
  • Dynamic Tape (DT)
Comparateur factice: Sham Taping

Fifteen competitive volleyball players were assigned to the sham taping group. Dynamic Tape was applied without tension as a straight I-strip along the lateral aspect of the dominant upper arm, with the shoulder in a neutral position. This application was intended to provide cutaneous stimulation without the directional mechanical support of the active taping technique. Participants were assessed under both taped and untaped conditions, with the taped assessment performed 45 minutes after application.

Dynamic Tape was applied without tension as a straight I-strip extending distally from the shoulder joint along the lateral upper arm, with the shoulder maintained in a neutral position. The sham technique was intended to preserve cutaneous stimulation while minimizing the mechanical support associated with the active taping technique.

Autres noms:
  • Sham taping (ST)

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Serve Velocity
Délai: During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.

Serve velocity was measured using a handheld radar gun (Bushnell Speed Radar Gun, Model 101911). Participants performed three successful maximal-effort serves under both taped and untaped conditions. The mean velocity of the three successful serves was calculated for each condition. Serve velocity was recorded in kilometers per hour (km/h).

During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Isometric Shoulder Internal Rotation Strength
Délai: During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.

Isometric shoulder internal rotation strength was measured on the dominant arm using a MicroFET2 handheld dynamometer. Participants were positioned prone with the shoulder abducted to 90° and elbow flexed to 90°. Three maximal isometric contractions were performed using the break-test method, with 1-minute rest intervals. The mean peak force of the three trials was recorded in kilograms-force (kgf). Higher values indicate greater muscle strength.

During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Isometric Shoulder External Rotation Strength
Délai: During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.

Isometric shoulder external rotation strength was measured on the dominant arm using a MicroFET2 handheld dynamometer. Participants were positioned prone with the shoulder abducted to 90° and elbow flexed to 90°. Three maximal isometric contractions were performed using the break-test method, with 1-minute rest intervals. The mean peak force of the three trials was recorded in kilograms-force (kgf). Higher values indicate greater muscle strength.

During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Functional Throwing Performance Index (FTPI)
Délai: During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.

Functional throwing performance was assessed using the Functional Throwing Performance Index (FTPI). Participants repeatedly threw a ball at a 30 × 30 cm target positioned 120 cm above the floor from a distance of 4.5 m for 30 seconds. FTPI was calculated as the percentage of successful throws relative to the total number of throws. Three trials were performed with 1-minute rest intervals, and the mean FTPI percentage was used for analysis. Higher scores indicate greater throwing accuracy.

During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Athlete Satisfaction With Taping
Délai: Once, immediately after completion of all performance assessments (Day 1).

Athlete satisfaction with the assigned taping intervention was assessed once after completion of all performance assessments. Participants rated their overall satisfaction specifically with the taped condition using a study-specific, single-item, 11-point numerical rating scale ranging from 0 (not satisfied at all) to 10 (completely satisfied). Higher scores indicate greater satisfaction with the taping intervention.

Once, immediately after completion of all performance assessments (Day 1).

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: SERDAR DEMİRCİ, PhD, Balikesir University

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

3 février 2025

Achèvement primaire (Réel)

18 avril 2025

Achèvement de l'étude (Réel)

18 avril 2025

Dates d'inscription aux études

Première soumission

27 octobre 2026

Première soumission répondant aux critères de contrôle qualité

30 octobre 2026

Première publication (Réel)

3 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

3 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

30 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 2024/60
  • 1919B012308879 (Autre subvention/numéro de financement: Scientific and Technological Research Council of Türkiye (TÜBİTAK) - 2209-A Student Research Projects Support Program)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

De-identified individual participant data underlying the results reported in this study, including serve velocity, shoulder rotator muscle strength, functional throwing performance, and athlete satisfaction, will be available from the corresponding author upon reasonable request for scientific research purposes, subject to applicable ethical and institutional requirements.

Délai de partage IPD

Beginning after publication, upon reasonable request

Critères d'accès au partage IPD

Researchers submitting a scientifically justified request, subject to ethical and institutional approval

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner