Comparing Blow Bottle and Acapella Techniques for Pneumonia Treatment
Comparative Effects of Blow Bottle and Acapella Along With Diaphragmatic Breathing in Patients With Pneumonia
This study is testing whether using Blow Bottle or Acapella techniques along with breathing exercises can help people aged 40-60 with pneumonia breathe better and feel improved.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 40 Years to 60 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06460610 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of two techniques, Blow Bottle and Acapella, combined with diaphragmatic breathing, in treating patients with pneumonia. The study focuses on patients aged 40-60 years who are experiencing acute pneumonia. By utilizing these techniques, the trial aims to improve airway clearance and oxygen saturation in patients suffering from this respiratory condition. The randomized design will help determine which method is more beneficial for managing pneumonia symptoms.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 40-60 years with acute pneumonia who are in unstable health conditions.
Not a fit: Patients with chronic respiratory conditions, severe pneumonia requiring immediate care, or those with physical or cognitive limitations may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance treatment options for pneumonia, potentially leading to better recovery outcomes for patients.
How similar studies have performed: While there is limited information on the specific combination of these techniques, similar approaches in respiratory therapy have shown promise in improving patient outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients in the acute pneumonia * Age40-60 years. * Both male and female * Patients with unstable health conditions * Participants were willing to participate Exclusion Criteria: * Patients with physical or cognitive limitations. * Patients with a history of chronic respiratory conditions such as COPD, bronchitis, or asthma * Pregnant or breastfeeding women. Individuals with musculoskeletal or neurological conditions * Patients with contraindications to chest percussion therapy, such as recent surgery or trauma to the chest area. * Patients with severe Pneumonia requiring immediate care
Where this trial is running
Lahore, Punjab Province
- Jinnah hospital Lahore — Lahore, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Sidra Afzal, PP-DPT — Riphah International University
- Study coordinator: Iqbal Tariq, Phd
- Email: iqbal.tariq@riphah.edu.pk
- Phone: 03338236752
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.