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NCT Number: NCT07647302

Acute Effects of Active and Passive Breaks 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.

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Key information

Age range

20 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hafez Taplux Group

Istanbul, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Active Break Exercises

Behavioral

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.

Primary outcomes

  1. Cervical Range of Motion

    Time frame: 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.

Secondary outcomes

  1. Shoulder Range of Motion

    Time frame: 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.

  2. Visual Analog Scale (VAS)

    Time frame: 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.

  3. Neck Disability Index (NDI)

    Time frame: 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.

  4. Checklist Individual Strength - Turkish Version (CIS-T)

    Time frame: 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Gözde Başbuğ, PhD,PT

CONTACT

[email protected]

Seyedeh simin Ashraftalesh, BSc,PT

CONTACT

[email protected]

+90 5387782429

Sponsors and collaborators

Lead sponsor

Istanbul Aydın University

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 15, 2026
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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