- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07647302
Acute Effects of Active and Passive Breaks in Office Workers
Investigation of the Acute Effects of Active and Passive Break Applications on Range of Motion, Neck Functionality, Pain and Fatigue Levels in Office Workers
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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 di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Seyedeh simin Ashraftalesh, BSc,PT
- Numero di telefono: +90 5387782429
- Email: siminashraf1377@gmail.com
Backup dei contatti dello studio
- Nome: Gözde Başbuğ, PhD,PT
- Email: gozdebasbug@aydin.edu.tr
Luoghi di studio
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Istanbul, Turchia (Türkiye)
- Hafez Taplux Group
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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.
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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.
|
|
Nessun intervento: 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.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Cervical Range of Motion
Lasso di tempo: Baseline and post-intervention (at the end of 5 working days)
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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.
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Baseline and post-intervention (at the end of 5 working days)
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Shoulder Range of Motion
Lasso di tempo: Baseline and post-intervention (at the end of 5 working days)
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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.
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Baseline and post-intervention (at the end of 5 working days)
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Visual Analog Scale (VAS)
Lasso di tempo: Baseline and post-intervention (at the end of 5 working days)
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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.
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Baseline and post-intervention (at the end of 5 working days)
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Neck Disability Index (NDI)
Lasso di tempo: Baseline and post-intervention (at the end of 5 working days)
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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.
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Baseline and post-intervention (at the end of 5 working days)
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Checklist Individual Strength - Turkish Version (CIS-T)
Lasso di tempo: Baseline and post-intervention (at the end of 5 working days)
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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.
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Baseline and post-intervention (at the end of 5 working days)
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Gözde Başbuğ, PhD,PT, Istanbul Aydın University
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- İAU-FTR-SSA-01
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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 .
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