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Acute Effects of Active and Passive Breaks in Office Workers

10. Juni 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

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

Interventionell

Einschreibung (Geschätzt)

40

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

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

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
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.
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Cervical Range of Motion
Zeitfenster: 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)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Shoulder Range of Motion
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Gözde Başbuğ, PhD,PT, Istanbul Aydın University

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

15. Juni 2026

Primärer Abschluss (Geschätzt)

22. Juni 2026

Studienabschluss (Geschätzt)

1. August 2026

Studienanmeldedaten

Zuerst eingereicht

10. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

10. Juni 2026

Zuerst gepostet (Tatsächlich)

15. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

15. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

10. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • İAU-FTR-SSA-01

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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