- ICH GCP
- US-Register für klinische Studien
- Klinische Studie 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
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Seyedeh simin Ashraftalesh, BSc,PT
- Telefonnummer: +90 5387782429
- E-Mail: siminashraf1377@gmail.com
Studieren Sie die Kontaktsicherung
- Name: Gözde Başbuğ, PhD,PT
- E-Mail: gozdebasbug@aydin.edu.tr
Studienorte
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Istanbul, Türkei (türkiye)
- Hafez Taplux Group
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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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.
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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.
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Kein Eingriff: 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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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Cervical Range of Motion
Zeitfenster: 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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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Shoulder Range of Motion
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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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Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Gözde Başbuğ, PhD,PT, Istanbul Aydın University
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- İAU-FTR-SSA-01
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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