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Combined Effects of Blow Bottle Device and Postural Drainage in Moderate to Severe Elderly COPD Patients

Not Applicable
Recruiting
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Other: percussion
Other: blow bottle technique
Registration Number
NCT06476769
Lead Sponsor
Riphah International University
Brief Summary

It will be a randomized clinical trial. Age of selected subjects will be between 40 to 70 years. Data will be collected from Wazirabad institute of cardiology. There will be 2 groups i.e. group A will receive combination of blow bottle technique and postural drainage and group B will receive postural drainage. Spirometer will be used to evaluate pulmonary functions and breathless, cough and sputum scale (BCSS) will be used to evaluate the improvement in sputum diary of patients. Interventions will be given to the patients for 20-25 minutes twice a day for 6 days per week. After data collection, data will be analyzed using SPSS version 25.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Diagnosed moderate to severe GOLD (2017) COPD
  • 40-60 years old
  • Both male and female
  • Patients hemodynamically stable
  • PFT showing irreversible airflow limitation.
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Exclusion Criteria
  • Type II diabetic mellitus
  • Systemic illness
  • Thoracic deformation or rib fracture.
  • Pulmonale decompensation and signs of an unstable heart condition.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
percussionpercussionThere were 20 patients in group B received postural drainage with percussion for 20- 25 minutes per session twice a day for 4 days per week, for 8 weeks.
blow bottle techniqueblow bottle techniqueThere were 20 patients in group A received blow bottle device and postural drainage for 20- 25 minutes per session twice a day for 4 days per week, for 8 weeks.
Primary Outcome Measures
NameTimeMethod
Incentive spirometry4 weeks

Incentive spirometry is frequently used after thoracic surgery as an adjunct to physiotherapy. Despite its widespread use, it has remained challenging to demonstrate a clinical benefit in terms of either incidence of pulmonary complications or hospital stay.

Breathlessness cough sputum scale4 weeks

Breathlessness, Cough and Sputum scale (BCSS) was developed to effectively measure the severity of respiratory symptoms. The BCSS records symptoms in a 5-point Likert like scale in which zero represents improvement symptoms and scores towards 4 indicating worsening of symptoms. It is commonly used in patients with COPD. BCSS provides a simple and robust quantification of symptoms that is sensitive to the effects of treatment and could therefore be used to assess therapeutic interventions. It has good reliability and validity for use in patients with respiratory disorders.

Modified borg RPE scale:4 weeks

The Modified Borg Dyspnea Scale (MBS) is rated numerical score used to measure dyspnea as reported by the patient during submaximal exercise, one of the most common and frequently used measures to assess the severity of dyspnea.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Wazirabad Institute of Cardiology

🇵🇰

Multān, Punjab, Pakistan

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