Actively Recruiting

Phase Not Applicable
Age: 45Years - 55Years
MALE
NCT06673953

Effect of Respiratory Trainer on Cardiopulmonary Functions in Patients with Upper Cross Syndrome Post-Cardiac Surgery

Led by Cairo University · Updated on 2024-11-05

60

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to investigate if there is any effect of the respiratory training on cardiopulmonary functions in patients with upper cross syndrome post-cardiac surgery. Hypothesis: Null hypothesis: There is no effect of the respiratory training on pulmonary functions in patients with upper cross syndrome post-cardiac surgery.

CONDITIONS

Official Title

Effect of Respiratory Trainer on Cardiopulmonary Functions in Patients with Upper Cross Syndrome Post-Cardiac Surgery

Who Can Participate

Age: 45Years - 55Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male patients aged 45 to 55 years
  • At least three months post-coronary artery bypass graft surgery
  • Craniovertebral angle less than 51 degrees but not less than 30 degrees
  • Chronic neck pain without a known pathological cause and no arm pain
  • Pain severity score between 3 and 7 on the Visual Analog Scale
  • Body mass index between 25 and 29.9 kg/m2
  • Forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC) below 80%
Not Eligible

You will not qualify if you...

  • Rheumatoid arthritis, cervical disc disease, or traumatic neck pain
  • History of respiratory disease or severe heart problems
  • Neurological disorders affecting the diaphragm
  • Body mass index less than 25 or greater than 30 kg/m2
  • Smokers
  • Forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC) above 80%
  • Chronic obstructive pulmonary disease or asthma

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

Faculty of Physical Therapy, Cairo University

Giza, Giza Governorate, Egypt, 11432

Actively Recruiting

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Research Team

M

Mostafa Ali

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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