Actively Recruiting

Phase Not Applicable
Age: 20Years - 40Years
All Genders
NCT06530056

Costovertebral Mobilization on Kyphotic Posture and Lung Function in Non-Smoker

Led by Riphah International University · Updated on 2024-08-14

44

Participants Needed

1

Research Sites

22 weeks

Total Duration

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AI-Summary

What this Trial Is About

Aim of this study is to find the effects of Costoverterbral Mobilization on Thoracic kyphosis and Lung function in non-smoker. A randomized control trial that will include total 44 participants.The first group will receive Costovertebral Mobilization along with conventional therapy and 2nd group will receive conventional therapy.Data collected will be analyzed through SPSS 25

CONDITIONS

Official Title

Costovertebral Mobilization on Kyphotic Posture and Lung Function in Non-Smoker

Who Can Participate

Age: 20Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Non smoker
  • Age between 20 and 40 years
  • Normal Body Mass Index between 18.5 and 24.9
  • Both female and male gender
  • Forced expiratory volume in one second to forced vital capacity ratio greater than or equal to 70%
  • Thoracic kyphotic posture greater than or equal to 40 degrees
Not Eligible

You will not qualify if you...

  • Any respiratory disease such as asthma, chronic bronchitis, COPD, or emphysema
  • Previous rib fractures, dislocations, or sprains of costochondral, costosternal, or interchondral joints
  • Smokers
  • Scheuermann Disease
  • Primary or secondary tumors of the spine or ribs
  • Advanced spinal deformities such as kyphoscoliosis
  • Infections such as tuberculosis
  • Primary or secondary tumors of chest soft tissues
  • Inflammatory conditions like acute rheumatoid arthritis or ankylosing spondylitis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Madiha Ali

Islamabad, Pakistan, 44000

Actively Recruiting

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Research Team

M

Madiha Ali, MSOMPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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