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Acute Effects of Active and Passive Breaks in Office Workers

16. juni 2026 oppdatert av: 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.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

40

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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Studiekontakt

Studer Kontakt Backup

Studiesteder

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Ingen inngripen: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Cervical Range of Motion
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Shoulder Range of Motion
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)

Samarbeidspartnere og etterforskere

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Etterforskere

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

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

15. juni 2026

Primær fullføring (Antatt)

22. juni 2026

Studiet fullført (Antatt)

1. august 2026

Datoer for studieregistrering

Først innsendt

10. juni 2026

Først innsendt som oppfylte QC-kriteriene

10. juni 2026

Først lagt ut (Faktiske)

15. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

16. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • İAU-FTR-SSA-01

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

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Studerer et amerikansk FDA-regulert medikamentprodukt

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Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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