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Clinical Trials in Turkey / NCT07647302
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Acute Effects of Active and Passive Breaks in Office Workers

NCT07647302 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-15
Last updated
2026-06-18

Condition(s) studied

Office Workers

Investigational drug(s) / intervention(s)

Active Break Exercises

Active Break Exercises: 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.

Study summary

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.

Eligibility

Sex
ALL
Min age
20 Years
Max age
55 Years
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hafez Taplux Group Istanbul Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07647302 on ClinicalTrials.gov ↗ ← All trials in Turkey