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Comparison of Upper Extremity Functions of Physiotherapy Students

13 de julio de 2026 actualizado por: Özge Mine Yilmaz

Comparison of Upper Extremity Functions of Physiotherapy Students With Different Hand Preferences

The purpose of this cross-sectional, comparative study is to comprehensively evaluate and compare upper extremity functions among physiotherapy students with different hand preferences. Handedness is a fundamental neuromotor characteristic that significantly influences upper extremity functions, including muscle strength, motor skills, coordination, and movement speed. These differences in motor performance can have prominent implications in professional fields like physiotherapy and rehabilitation, which demand a high level of manual dexterity, hand-eye coordination, and precise motor control during clinical applications.

While previous literature has predominantly focused on isolated measures such as grip strength, multi-dimensional studies that concurrently evaluate hand preference, objective motor performance, strength, and self-reported functional status remain limited. This study aims to fill this gap by determining whether significant differences exist in strength, performance, and functional levels between right-handed and left-handed individuals within a specialized student population.

A total of 42 physiotherapy and rehabilitation students aged 18 and older will be recruited through convenient sampling. Hand preference and lateralization will be objectively determined using the Edinburgh Handedness Inventory, categorizing participants based on their Laterality Quotient (LQ). Upper extremity functional levels, manual dexterity, and strength will be thoroughly evaluated. Self-reported upper extremity disability will be measured using the Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) questionnaire. Performance-based manual dexterity and functional capacity will be objectively assessed using the Jebsen-Taylor Hand Function Test, which measures the time taken to complete seven simulated activities of daily living. Gross grip strength will be measured with a Jamar hand dynamometer, and fine pinch strength will be quantified using a pinchmeter. All assessments will be performed under standardized environmental conditions with dedicated, trained assessors to ensure high measurement reliability. The outcomes will provide critical insights into neuromotor control strategies and potential ergonomic adjustments needed for left-handed students during their clinical training.

Descripción general del estudio

Estado

Aún no reclutando

Tipo de estudio

De observación

Inscripción (Estimado)

42

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

  • Adulto

Acepta Voluntarios Saludables

Sí

Método de muestreo

Muestra no probabilística

Población de estudio

The study population consists of undergraduate students studying in the Department of Physiotherapy and Rehabilitation, who are healthy volunteers and stratified into groups based on their hand preferences (right-handed vs. left-handed).

Descripción

Inclusion Criteria:

  • Being a student currently enrolled in the Department of Physiotherapy and Rehabilitation.
  • Being aged 18 years or older.
  • Voluntary participation with signed informed consent.

Exclusion Criteria:

  • Having a history of orthopedic surgery, severe trauma, or structural deformity in the upper extremities.
  • Diagnosis of any neurological, rheumatological, or systemic disease that permanently affects upper extremity motor functions or muscle strength.
  • Presence of acute pain, injury, or active inflammatory conditions in the dominant or non-dominant upper extremity within the last 3 months.
  • Sensory deficits or uncorrected visual impairments that prevent understanding or performing the functional tests.

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

Cohortes e Intervenciones

Grupo / Cohorte
Right-handed Physiotherapy Students
Left-handed Physiotherapy Students

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Manual Dexterity and Hand Function
Periodo de tiempo: At baseline (single session assessment)
Assessed using the Jebsen-Taylor Hand Function Test (JTHFT), which consists of seven subtests simulating daily activities (writing, card turning, picking up small objects, stacking checkers, simulated eating, moving light objects, and moving heavy objects). The completion time for each subtest is recorded in seconds, with shorter times indicating better functional performance.
At baseline (single session assessment)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Grip and Pinch Strength
Periodo de tiempo: At baseline (single session assessment)
Gross grip strength is measured in kilograms using a Jamar hand dynamometer, and fine pinch strength is quantified using a pinchmeter. The average of three trials for each measurement is recorded
At baseline (single session assessment)
Self-Reported Upper Extremity Disability
Periodo de tiempo: At baseline (single session assessment)
Assessed using the Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) questionnaire. It is an 11-item self-report tool where total scores are converted to a scale ranging from 0 to 100. A score of 0 indicates no disability (best possible outcome), while a score of 100 represents the most severe upper extremity disability (worse outcome). Higher scores mean worse functional limitation.
At baseline (single session assessment)

Colaboradores e Investigadores

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

Patrocinador

Colaboradores

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 (Estimado)

1 de agosto de 2026

Finalización primaria (Estimado)

30 de agosto de 2026

Finalización del estudio (Estimado)

5 de septiembre de 2026

Fechas de registro del estudio

Enviado por primera vez

7 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

7 de julio de 2026

Publicado por primera vez (Actual)

13 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

14 de julio de 2026

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

13 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • IstanbulAUu

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. .

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