MedPath

A Study of short-term effects of using shoulder-posture-corrector belts combined with stretching exercise in the management of chronic neck pain in office workers: A randomized single-blind controlled trial

Phase 2
Completed
Conditions
Office workers with chronic moderate degree of non-specific neck pain
Neck pains, office workers, shoulder brace
Registration Number
TCTR20230708001
Lead Sponsor
Faculty of Medicine Siriraj Hospital, Mahidol University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
60
Inclusion Criteria

1. Office workers with continuous or intermittent neck pain for at least 3 months, 2. Severity of pain is moderate degree (NRS 3-8 from 10), 3. Sitting duration during working at least 4 hours per day

Exclusion Criteria

1. Diagnosed other causes of neck pain, 2. Receive physical therapy, massage or needling for treatment neck pain within 1 week, 3. Using medication (Paracetamol, NSAIDs, muscle relaxant, opiod) within 1 week, 4. History of severe neck injury, 5. History of neck or shoulder injury, 5. Diagnosed disease of shoulder, 6. Presentation of severe psychiatric disorder, 7. Being pregnancy, 8. Cannot answer the questionnaire due to communication problem, 9. Schedule for taking a leave during 2 weeks of study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
eck pain score at 2 weeks after end of the intervention Visual analogue scale
Secondary Outcome Measures
NameTimeMethod
Cervical range of motion at 2 weeks after end of the intervention Double inclinometers,Forward head posture at 2 weeks after end of the intervention Craniovertebral angle,Neck disability at 2 weeks after end of the intervention Neck disability index thai version,Satisfaction for treatment at 2 weeks after end of the intervention satisfaction likert scale,Compliance of treatment at 2 weeks after end of the intervention Hour of using device per day,Side effect of device using at 2 weeks after end of the intervention Description
© Copyright 2025. All Rights Reserved by MedPath