Combined Effects of Balloon Blowing Therapy With Percussion in Patients With Pneumonia
1 other identifier
interventional
40
1 country
1
Brief Summary
Pneumonia is an infection of the lungs that is caused by bacteria, viruses, fungi, or parasites. It is characterized primarily by inflammation of the alveoli in the lungs or by alveoli that are filled with fluid (alveoli are microscopic sacs in the lungs that absorb oxygen). The symptoms of pneumonia can develop suddenly (over 24-48 hours) or may show more slowly, over several days. Common symptoms of pneumonia are likely to have a cough which can be dry, or may produce phlegm (thick mucus) that is yellow, green, brownish or bloodstained and breathing difficulty, wheezing and chest tightness where the rate will be high and the rhythm will be rapid and shallow. This activity encourages deep breathing, allowing a patient body to relax. Explain the patient that this exercise will help him or he can feel more relaxed. Make the patient to imagine that he/she is blowing up a balloon. Ask him/her to take in a deep breath; steadily and slowly blow up the huge balloon. See the balloon getting bigger, and bigger. Now ask the patient to close the eyes and imagine the balloon floating into the air. Let the patient continue blowing of balloons until he or she gets relaxed and calm. Percussion is a technique involving rhythmic tapping or clapping on the chest or back, serves as a means to move and loosen retained secretions within the airways. This mechanical intervention helps in removing mucus from the bronchial walls, and facilitates its expectoration and clearance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 30, 2024
CompletedFirst Submitted
Initial submission to the registry
June 11, 2024
CompletedFirst Posted
Study publicly available on registry
June 14, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 10, 2024
CompletedJune 14, 2024
June 1, 2024
1 month
June 11, 2024
June 11, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
FEV1(Forced Expiratory Volume per second)
Pulmonary Function Test using Digital Spirometer
Pre and post after 1 week
FVC (Forced Vital Capacity)
Pulmonary Function Test using Digital Spirometer
Pre and Post after 1 week
FEV1/FVC
Pulmonary Function Test using Digital Spirometer
Pre and Post after 1 week
CASA-Q (Cough and Sputum Assessment Questionnaire)
To assess the Level of Cough and Sputum
Pre and post after 1 week
Auscultatory Breath Sound
To assess the breath sound
pre and Post after 1 week
Study Arms (2)
Balloon Blowing, Percussion
EXPERIMENTALintervention will be given as blowing 10-15 balloons per day for 6 days. 05.minutes active cycle of breathing technique as baseline 10 minute to blowing 15 balloons 10 minutes percussion 25 minutes session
Perccussion
ACTIVE COMPARATORintervention Will be given as Buteyko breathing techniques for 3 weeks. 15 Minutes ACBT with rest interval 10 minutes percussion 25 minutes session
Interventions
Ask the patient to take in a deep breath; steadily and slowly blow up the huge balloon. See the balloon getting bigger, and bigger. Now ask the patient to close the eyes and imagine the balloon floating into the air. Let the patient continue blowing of balloons until he or she gets relaxed and calm.
Percussion is a technique involving rhythmic tapping or clapping on the chest or back, serves as a means to move and loosen retained secretions within the airways. This mechanical intervention helps in removing mucus from the bronchial walls, and facilitates its expectoration and clearance
Eligibility Criteria
You may qualify if:
- Diagnosed pneumonia patients
You may not qualify if:
- Other respiratory complications
- Patients with surgeries
- Patients with neurological disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Lahore Teaching hospital
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Tasneem Shehzadi, Mphil
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 11, 2024
First Posted
June 14, 2024
Study Start
May 30, 2024
Primary Completion
June 30, 2024
Study Completion
July 10, 2024
Last Updated
June 14, 2024
Record last verified: 2024-06
Data Sharing
- IPD Sharing
- Will not share