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Acute Effects of Shoulder Dynamic Taping in Competitive Volleyball Players

30 ottobre 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Effettivo)

30

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

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

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

Da 18 anni a 35 anni (Adulto)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Femmina

Descrizione

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.

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: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.

Altri nomi:
  • Dynamic Tape (DT)
Comparatore fittizio: 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.

Altri nomi:
  • Sham taping (ST)

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Serve Velocity
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Isometric Shoulder Internal Rotation Strength
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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).

Collaboratori e investigatori

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

Sponsor

Collaboratori

Investigatori

  • Investigatore principale: SERDAR DEMİRCİ, PhD, Balikesir University

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo 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)

3 febbraio 2025

Completamento primario (Effettivo)

18 aprile 2025

Completamento dello studio (Effettivo)

18 aprile 2025

Date di iscrizione allo studio

Primo inviato

27 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 ottobre 2026

Primo Inserito (Effettivo)

3 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

3 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 ottobre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2024/60
  • 1919B012308879 (Altro numero di sovvenzione/finanziamento: Scientific and Technological Research Council of Türkiye (TÜBİTAK) - 2209-A Student Research Projects Support Program)

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 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.

Periodo di condivisione IPD

Beginning after publication, upon reasonable request

Criteri di accesso alla condivisione IPD

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

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO

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 .