Comparing blow bottle technique and active cycle of breathing in COPD patients
Effects of Blow Bottle Verses ACBTs Technique in Patients of Chronic Obstructive Pulmonary Disease
NA · Riphah International University · NCT06189196
This study is testing whether the blow bottle technique or the active cycle of breathing helps people with COPD breathe better and feel healthier.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 48 (estimated) |
| Ages | 45 Years to 65 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Lahore, Punjab) |
| Trial ID | NCT06189196 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effects of the blow bottle technique and the active cycle of breathing techniques (ACBT) on patients with chronic obstructive pulmonary disease (COPD). The study will involve 56 patients who will be randomly assigned to either the blow bottle group or the ACBT group. Key outcomes will include measurements of sputum production, oxygen saturation, pulmonary function, and quality of life. The trial will take place at Gulab Devi Hospital in Lahore, Pakistan.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 45 to 65 with moderate COPD and a history of chronic sputum production.
Not a fit: Patients with other pulmonary diseases, such as bronchiectasis or lung cancer, will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more effective and economical treatment option for managing symptoms and improving quality of life in COPD patients.
How similar studies have performed: While there is existing research on pulmonary rehabilitation techniques, the specific comparison of blow bottle technique and ACBT in COPD patients is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Moderate COPD * Hx of chronic sputum production * Regular expectoration * After 48 hours of admission in hospital * Patient of 45 to 65 years * Both genders (male and female) Exclusion Criteria: * Pulmonary disease like, Bronchiectasis, pneumothorax, TB, atelectasis * Lung Abscess * Lung cancer * Any post-surgical (pneumectomy, lobectomy) * Hemoptysis
Where this trial is running
Lahore, Punjab
- Gulab Devi Hospital — Lahore, Punjab, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Wajeeha Zia, phd* — Riphah International University
- Study coordinator: Imran Amjad, phd
- Email: imran.amjab@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: COPD, Active cycle of breathing technique, Breathlessness, Cough, Chronic Obstructive Pulmonary Disease,, Sputum, Quality Of Life