Actively Recruiting

Phase Not Applicable
Age: 40Years - 60Years
All Genders
NCT06461884

Combined Effects Of Percussion With Diaphragmatic Breathing Exercises On Airway Clearance In Elderly Pneumonia Patients

Led by Riphah International University · Updated on 2024-06-17

40

Participants Needed

1

Research Sites

18 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The group A will receive percussions and diaphragmatic breathing with 1 session a day for 3 days in a week for 4 weeks. In this way total 12 sessions will be given to the patients. And group B will receive only diaphragmatic breathing with 1 session a day for total 3 days in a week for 4 weeks. By this intervention procedure, I will find out the effects of these techniques on airway clearance of the pneumonia patients, their effect on the quality of life and on Dyspnea. For this I will use 4 tool questionnaires that are 1-BCSS, 2- Modified Borg Dyspnea scale, 3-Rate of perceived exertion scale, 4- Health-related Quality of Life-14. BCSS will be used to assess breathlessness, cough and sputum retention. Modified Borg Dyspnea scale is 0-10 rated numerical scale used to measure Dyspnea. RPE is a way to measure the level of exertion a person feels during physical activity. HRQOL-14 will assess the quality of life of the pneumonia patients.

CONDITIONS

Official Title

Combined Effects Of Percussion With Diaphragmatic Breathing Exercises On Airway Clearance In Elderly Pneumonia Patients

Who Can Participate

Age: 40Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 40 to 60 years
  • Both males and females
  • Patients who are vitally stable with normal oxygen saturation and respiratory rate
  • Patients diagnosed with community-acquired pneumonia
Not Eligible

You will not qualify if you...

  • Patients with heart disease
  • Patients with neurological disorders such as Alzheimer’s, epilepsy, or Parkinson’s disease
  • Patients with orthopedic conditions
  • Patients with other pulmonary complications such as atelectasis, diaphragmatic injury, or ARDS

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

Mayo Hospital Lahore

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

I

Iqbal Tariq, PHD

CONTACT

I

imran amjad, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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