Viewing Study NCT04828837



Ignite Creation Date: 2024-05-06 @ 3:58 PM
Last Modification Date: 2024-10-26 @ 2:01 PM
Study NCT ID: NCT04828837
Status: TERMINATED
Last Update Posted: 2022-04-14
First Post: 2021-02-25

Brief Title: Bubble PEP Training Among Patient With Chronic Obstructive Pulmonary Disease in Pulmonary Function Effects
Sponsor: National Taipei University of Nursing and Health Sciences
Organization: National Taipei University of Nursing and Health Sciences

Study Overview

Official Title: National Taipei University of Nursing and Heath Sciences
Status: TERMINATED
Status Verified Date: 2022-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Due to the SARS-CoV-2 pandemic in Taiwan in 202105 and then recruitment was stopped under the government epidemic prevention policy
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The morbidity rate of Chronic Obstructive Pulmonary Disease COPD is increasing year by year It is predicted to be the third leading cause of death worldwide in 2030 People with COPD have a high risk of needing a ventilator due to the decline of lung function the increase of secretions the dysfunction of airway clearance and the obstruction and loss of alveolar elasticity
Detailed Description: This study aimed to explore the effectiveness of cough and sputum assessment and respiratory physiological indicators after training with the Bubble positive expiratory pressure Bubble PEP inpatients with COPD This is a randomization control trial design survey using convenient sampling and will be to select 94 inpatients with COPD in the division of chest ward of two teaching hospital in New Taipei City The subjects who meet the conditions for admission are explained and they need to sign a consent form confirming that they understand the risks More they are randomly divided into the experimental group experimental group n47 and the control group control group n47 The experimental group receives the Bubble PEP training the control group receives the division of chest ward routine care The study employs a structured questionnaire including a basic demography COPD domain COPD assessment test CAT cough and sputum assessment test and check the peak expiratory flow rate PEFR using it for data collection The study needs to be approve by the Institutional Review Board The two groups agreed to participate in the study after completing the subject consent form before the intervention they also received the pre-test as a benchmark for the intervention effect After completing the 7-day and 30-day intervention the post-test was performed immediately to understand the intervention immediate effect

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