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Acute Effects of Active and Passive Breaks in Office Workers

16 de junio de 2026 actualizado por: Seyedeh Simin Ashraftalesh, Istanbul Aydın University

Investigation of the Acute Effects of Active and Passive Break Applications on Range of Motion, Neck Functionality, Pain and Fatigue Levels in Office Workers

The purpose of this study is to investigate the acute effects of active and passive break applications during work hours on cervical and shoulder range of motion (ROM), neck functionality, pain intensity, and fatigue levels among office workers. Participants are randomly assigned to either an Active Break Group, performing structured exercises, or a Control Group with passive rest over a 5-day protocol.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

Prolonged sitting and sustained static postures during computer use are significant occupational health hazards for office workers, frequently leading to cumulative mechanical loading, localized muscle fatigue, and functional impairments in the neck and shoulder regions. Continuous isometric muscle activity during desk work increases intramuscular pressure and reduces local circulation, which consequently decreases joint range of motion, restricts neck functionality, and elevates subjective fatigue levels. While traditional passive rest breaks (sitting quietly) are commonly utilized, they often fall short of mitigating these sedentary stress factors. In contrast, structured active rest breaks involving dynamic movement and stretching can trigger a "muscle pump" mechanism, enhance tissue oxygenation, lower viscoelastic stiffness, and systematically reduce fatigue and pain perceptions.

Although long-term exercise interventions are well-documented, clinical trials directly comparing the acute, immediate impacts of structured active breaks versus passive rest strategies on multi-dimensional outcomes remain limited. To address this methodological gap, this randomized controlled trial evaluates and compares the acute effects of active and passive break applications among office workers who work at a desk for at least 5 hours a day. Participants are randomly allocated into two parallel arms: the Active Break Group and the Control (Passive Break) Group. The intervention protocol spans a total of 5 working days, with both groups taking a 5-minute designated break every hour. The Active Break Group performs structured stretching and mobility exercises targeted at the cervical and shoulder regions under physiotherapist supervision, while the Control Group rests quietly at their workstations. Objective and subjective assessments are conducted at baseline and immediately following the 5-day protocol using cervical and shoulder range of motion (ROM) measurements via a goniometer, the Visual Analog Scale (VAS) for pain intensity, the Neck Disability Index (NDI) for neck functionality, and the Checklist Individual Strength (CIS-T) questionnaire to determine acute fatigue levels.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

40

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.

Estudio Contacto

  • Nombre: Seyedeh simin Ashraftalesh, BSc,PT
  • Número de teléfono: +90 5387782429
  • Correo electrónico: siminashraf1377@gmail.com

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

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

No

Descripción

Inclusion Criteria:

  • Being between 20 and 55 years of age
  • Working at a desk while seated for at least 5 hours a day
  • Not participating in high-intensity physical activity regularly
  • Volunteering to participate in the study and providing informed consent

Exclusion Criteria:

  • History of recent trauma or surgery directed at the cervical or thoracic regions
  • Current state of pregnancy
  • Diagnosis of diabetes or similar chronic systemic diseases
  • Presence of any cognitive or physical limitation that could affect exercise performance or assessments

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Active Break Group
The active break intervention is performed for 5 minutes every hour during the workday for a total of 5 working days. Under the supervision of a physiotherapist, participants perform structured active rest breaks consisting of stretching and mobility exercises targeted at the cervical and shoulder regions. The protocol includes: cervical flexion, extension, lateral flexion, and rotation stretches; upper trapezius stretching, pectoral stretching, posterior capsule stretching; shoulder shrugs, shoulder rolls, and scapular retraction exercises. Each exercise is performed either as a 15-second stretch or completed for 10 repetitions per session, always maintained within a safe and pain-free range of motion.
The active break intervention is performed for 5 minutes every hour during the workday for a total of 5 working days. Under the supervision of a physiotherapist, participants perform structured active rest breaks consisting of stretching and mobility exercises targeted at the cervical and shoulder regions. The protocol includes: cervical flexion, extension, lateral flexion, and rotation stretches; upper trapezius stretching, pectoral stretching, posterior capsule stretching; shoulder shrugs, shoulder rolls, and scapular retraction exercises. Each exercise is performed either as a 15-second stretch or completed for 10 repetitions per session, always maintained within a safe and pain-free range of motion.
Sin intervención: Passive Break Group
The passive break group takes a 5-minute passive rest break every hour during the workday for a total of 5 working days. During these designated break periods, participants remain seated quietly and rest at their workstations. They do not perform any physical exercises, stretching routines, or structured active movements, maintaining their usual sedentary work routine during the breaks.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Cervical Range of Motion
Periodo de tiempo: Baseline and post-intervention (at the end of 5 working days)
Cervical range of motion including flexion, extension, lateral flexion, and rotation will be measured in degrees using a goniometer to assess active neck mobility. Higher values in degrees indicate better cervical joint mobility.
Baseline and post-intervention (at the end of 5 working days)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Shoulder Range of Motion
Periodo de tiempo: Baseline and post-intervention (at the end of 5 working days)
Active shoulder range of motion (including flexion and abduction) will be measured in degrees using a goniometer to assess shoulder mobility. Higher values in degrees indicate better shoulder joint mobility.
Baseline and post-intervention (at the end of 5 working days)
Visual Analog Scale (VAS)
Periodo de tiempo: Baseline and post-intervention (at the end of 5 working days)
A 10-cm scale used to measure the subjective intensity of neck pain, where 0 indicates no pain and 10 indicates the worst possible pain.
Baseline and post-intervention (at the end of 5 working days)
Neck Disability Index (NDI)
Periodo de tiempo: Baseline and post-intervention (at the end of 5 working days)
A self-reported questionnaire with 10 items used to measure how neck pain affects functionality and daily life activities. Total scores range from 0 to 50, where higher scores indicate greater neck disability.
Baseline and post-intervention (at the end of 5 working days)
Checklist Individual Strength - Turkish Version (CIS-T)
Periodo de tiempo: Baseline and post-intervention (at the end of 5 working days)
A 20-item self-report questionnaire used to assess different aspects of fatigue, including subjective fatigue, concentration, motivation, and physical activity levels. Total scores range from 20 to 140, where higher scores indicate greater fatigue levels.
Baseline and post-intervention (at the end of 5 working days)

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Gözde Başbuğ, PhD,PT, Istanbul Aydın University

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)

15 de junio de 2026

Finalización primaria (Estimado)

22 de junio de 2026

Finalización del estudio (Estimado)

1 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

10 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

10 de junio de 2026

Publicado por primera vez (Actual)

15 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de junio de 2026

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

16 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • İAU-FTR-SSA-01

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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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