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Acute Effects of Shoulder Dynamic Taping in Competitive Volleyball Players

30 de octubre de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

30

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 35 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Femenino

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.

Otros nombres:
  • Dynamic Tape (DT)
Comparador falso: 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.

Otros nombres:
  • Sham taping (ST)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Serve Velocity
Periodo de tiempo: 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.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Isometric Shoulder Internal Rotation Strength
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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).

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: SERDAR DEMİRCİ, PhD, Balikesir University

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

3 de febrero de 2025

Finalización primaria (Actual)

18 de abril de 2025

Finalización del estudio (Actual)

18 de abril de 2025

Fechas de registro del estudio

Enviado por primera vez

27 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de octubre de 2026

Publicado por primera vez (Actual)

3 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

3 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

30 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2024/60
  • 1919B012308879 (Otro número de subvención/financiamiento: Scientific and Technological Research Council of Türkiye (TÜBİTAK) - 2209-A Student Research Projects Support Program)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan 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.

Marco de tiempo para compartir IPD

Beginning after publication, upon reasonable request

Criterios de acceso compartido de IPD

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

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .