Evaluation of Ergonomic Risks and the Effect of Patient Education on Musculoskeletal Complaints, Posture and Breathing Awareness in Bank Employees
1 other identifier
interventional
62
1 country
1
Brief Summary
This study aims to evaluate ergonomic risks among bank office employees and to investigate the effects of patient education and breathing exercises on musculoskeletal complaints, posture, ergonomic awareness and breathing awareness. Office workers often experience musculoskeletal problems due to prolonged sitting, poor posture and repetitive computer-based work. In this study, participants will be assessed using standardized questionnaires and ergonomic assessment methods before and after a eight-week intervention program. The intervention includes ergonomic education and breathing exercises delivered by a physiotherapist. The results of the study are expected to provide evidence on the effectiveness of ergonomic education and breathing exercises in improving musculoskeletal health and posture awareness among office workers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 19, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 6, 2026
CompletedFirst Submitted
Initial submission to the registry
March 15, 2026
CompletedFirst Posted
Study publicly available on registry
March 19, 2026
CompletedApril 16, 2026
April 1, 2026
2 months
March 15, 2026
April 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Musculoskeletal Pain Intensity
Musculoskeletal pain intensity will be assessed using the Visual Analog Scale (VAS). Participants rate their pain on a scale from 0 (no pain) to 10 (worst possible pain).
Baseline and 8 weeks
Ergonomic Risk Level
Ergonomic risk will be assessed using the Rapid Office Strain Assessment (ROSA) method to evaluate workstation ergonomics and office-related risk factors.
Baseline and 8 weeks
Secondary Outcomes (4)
Upper Limb Ergonomic Risk
Baseline and 8 weeks
Musculoskeletal Symptoms
Baseline and 8 weeks
Postural Awareness
Baseline and 8 weeks
Breathing Awareness
Baseline and 8 weeks
Study Arms (2)
Intervention Group
EXPERIMENTALParticipants in this arm will complete a 8-week multimodal intervention program supervised by a physical therapist, delivered twice weekly via synchronous video conferencing and video based modules. The program integrates individualized ergonomic education, informed by baseline ROSA and RULA risk assessments to optimize workstation setups, with a structured respiratory exercise protocol designed to enhance postural and breathing awareness. Each 30-40 minute session focuses on mitigating musculoskeletal strain and improving thoracic mobility. Clinical outcomes, including pain, postural and respiratory awareness , and ergonomic knowledge, will be reassessed at the end of the 8-week period to evaluate efficacy relative to baseline.
Control Group
NO INTERVENTIONThis group will not receive any active intervention, including respiratory exercises, ergonomic training, or patient education during the study period. Participants will only undergo baseline (pre-test) and follow-up (post-test) assessments.
Interventions
Educational sessions designed to increase awareness about workplace ergonomics, correct sitting posture and proper workstation setup for office workers.
Eligibility Criteria
You may qualify if:
- Aged between 20 and 55 years
- Working at a desk job
- Using a computer for at least 4 hours per day
- Employed in the same job for at least 6 months
- Voluntarily agreeing to participate in the study
You may not qualify if:
- History of musculoskeletal injury, trauma or surgery affecting the head, neck, back, shoulder, arm, leg or hand
- Pregnancy
- Presence of any medical condition affecting the musculoskeletal system
- Regular use of analgesic medication
- Diagnosis of psychiatric disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Uskudar University, Faculty of Health Sciences
Istanbul, 34662, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Filiz Eyuboglu, PhD
Uskudar University
- PRINCIPAL INVESTIGATOR
Mert İlhan, MSc.
Uskudar University
- PRINCIPAL INVESTIGATOR
Tuba Kolaylı Çerezci, MSc.
Uskudar University
- PRINCIPAL INVESTIGATOR
Mizgin Duygu, PT.
Uskudar University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 15, 2026
First Posted
March 19, 2026
Study Start
November 24, 2025
Primary Completion
January 19, 2026
Study Completion
March 6, 2026
Last Updated
April 16, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share