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Clinical Trials/NCT06240936
NCT06240936
Completed
N/A

Effects of Active Cycle of Breathing Techniques With and Without Acapella in COPD Patients

Riphah International University1 site in 1 country42 target enrollmentFebruary 15, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Riphah International University
Enrollment
42
Locations
1
Primary Endpoint
Sputum diary BCSS
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Chronic Obstructive Pulmonary Disease refers to a group of progressive lung diseases the block air flow and make it difficult to breath. It is potentially fatal and fourth leading cause of death in the world. The symptoms of this condition include shortness of breath, frequent coughing, fatigued and tightness in the chest. Due to the secretions in the lungs sometime patients will have great difficulty catching the breath after walking or exercise. Patient will also feel breathless just sitting or relaxing. Active Cycle of breathing technique can be used to mobilize and clear secretions. It will improve their stamina and reduce the episodes of breathlessness, help to remove the secretions from the lungs and feel better overall. Acapella is a small hand held device which help to loosen and clear secretions from the chest it has both resistive and vibratory features. A randomized control trial will be conducted at Gosha e Shifa hospital and General hospital Lahore through convenience sampling technique on 42 patients which will be allocated through simple random sampling through sealed opaque enveloped into group A and group B. Group A will be treated with active cycle of breathing exercises/techniques and Group B will be treated with Acapella device with active cycle of breathing exercise .Outcome measure will be conducted through Modified dyspnea scale, acapella device usage and questionnaire after 4 weeks and also perform Pulmonary function test .Data will be analyzed using SPSS software version 21. After assessing normality of data by Shapiro - wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups. Acapella device uses and active cycle of breathing technique will be applied for comparing their effect in patients of COPD.

Registry
clinicaltrials.gov
Start Date
February 15, 2024
End Date
April 15, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Both men and women age between 35-50 years.
  • Having smoking history .(1)
  • Dyspnea MRC scale grade 2 and grade 3.(20)
  • Gold standard COPD grade 2

Exclusion Criteria

  • Any kind of infective pulmonary condition .
  • Restrictive lung disease.(20)
  • Pregnancy.
  • Any severe heart disease

Outcomes

Primary Outcomes

Sputum diary BCSS

Time Frame: baseline and fourth week

In this diary we will check breathlessness, cough and sputum. It also includes the score of patient wellbeing and documented all minor symptoms

Modified Dyspnea scale.

Time Frame: baseline and fourth week

Data collection tool for shortness of breath is modified dyspnea scale there will be 10 readings. It also accesses breathing discomfort, sensory qualities and emotional distress.

PFTs

Time Frame: baseline and fourth week

The test will measure the lung volume, and ABGs. It is important tool for the investigation and monitoring of patients with respiratory pathology

Study Sites (1)

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