Comparison of Exercise With & Without Bracing in Office Workers With Kyphosis
- Conditions
- Kyphosis
- Registration Number
- NCT06867003
- Lead Sponsor
- Riphah International University
- Brief Summary
The study aims to Compare PT and bracing in improving posture, pain, and functionality in patient with kyphosis.
It also assess the additive benefits of combining PT with bracing. It also identify sustainable, non-surgical approaches for managing kyphosis in office
- Detailed Description
The study focuses on understanding Kyphosis, defined as excessive forward curvature of the thoracic spine, has become increasingly prevalent in modern work environments due to the sedentary nature of desk jobs. Kyphosis, characterized by a rounded upper back or "hunchback" appearance, is a clinical and postural problem with significant physical, functional, and psychosocial implications. Among office workers, the condition is primarily postural, driven by long hours of desk work, inappropriate ergonomic settings, and inadequate postural awareness. The increasing prevalence of kyphosis in this demographic has led to a pressing need for effective nonsurgical management strategies, including physical therapy (PT) and spinal bracing.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 36
- Office workers diagnosed with Postural Kyphosis
- age limit 30 to 45years
- Experience of upper back or neck pain lasting at least three months
- Spend a minimum of 6 hours per day in a seated position for work.
- History of spinal surgery, severe scoliosis, or other significant spinal deformities.
Current engagement in any structured physical therapy program or use of bracing for posture. Any neurological or musculoskeletal disorders impacting posture or movement.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Oswestry Disability Index (ODI) 4 weeks The questionnaire consists of 10 sections, each with 6 response options (scored 0 to 5). If all 10 sections are completed, the maximum score is 50.
Visual Analogue Scale (VAS) 4 weeks A 10 cm horizontal line with "No Pain" (0) on the left and "Worst Pain" (10) on the right.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (1)
Riphah international University malakand campus
🇵🇰Malakand, KPK, Pakistan