Viewing Study NCT06242210



Ignite Creation Date: 2024-05-06 @ 8:05 PM
Last Modification Date: 2024-10-26 @ 3:20 PM
Study NCT ID: NCT06242210
Status: COMPLETED
Last Update Posted: 2024-04-19
First Post: 2024-01-28

Brief Title: Effects of Pursed Lip Breathing Technique Versus Stacked Breathing Technique Among Chronic Bronchitis Patients
Sponsor: Riphah International University
Organization: Riphah International University

Study Overview

Official Title: Effects of Pursed Lip Breathing Technique Versus Stacked Breathing Technique on Dyspnea Lung Volumes Oxygenation and Quality of Life Among Chronic Bronchitis Patients
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Chronic bronchitis is a non-allergic inflammatory disease that is developed because of inflamed bronchial walls and is characterized by persistent cough with sputum for 3 months for 2 consecutive years at least It affects males more than females at the age of 40 years with increasing incidence as the age progresses Chronic bronchitis is associated with multiple health-related issues like dyspnea reduced lung volumes and capacities poor quality of life and physical inactivity Its clinical manifestations are coped with using the pharmaceutical approach surgical maneuvers and pulmonary rehabilitation In the context of pulmonary rehabilitation pursed lip breathing and stacked breathing are evident to deal with symptoms of chronic bronchitis and make the individuals lead a physically active and healthy life In this research study patients will be enrolled with strict adherence to eligibility criteria and then allocated into two groups by using the convenience sampling technique after having their written informed consent form The participants will either receive pursed lip breathing technique or a stacked breathing technique which will be followed by baseline treatment at every session Both groups will be then subjected to receive intervention that will take a duration of 40 minutes every session 30 minutes of baseline treatment and 10 minutes of intervention for the period of 2 weeks with the frequency of performing the intervention thrice per day The outcomes will be evaluated by using a modified Borg scale for dyspnea a peak expiratory flow meter for lung volumes a pulse oximeter for oxygenation and EuroQol 5D-5L for quality of life Data will be recorded at pre-treatment on the 1st day and post-treatment on the 14th day The recorded data will be then entered and analyzed using SPSS Statistical Package of Social Sciences version 23
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None