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Comparison of Exercise With & Without Bracing in Office Workers With Kyphosis

Not Applicable
Recruiting
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
Inclusion Criteria
  • 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.
Exclusion Criteria
  • 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
NameTimeMethod
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
NameTimeMethod

Trial Locations

Locations (1)

Riphah international University malakand campus

🇵🇰

Malakand, KPK, Pakistan

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