Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06519474
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-14
Brief Title:
Effect of Elastic Chest Compression on Functional Exercise Capacity and Respiratory Performance in Patients With COPD
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effect of Elastic Chest Compression on Functional Exercise Capacity and Respiratory Performance in Patients With COPD
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to investigate the effects of elastic chest compression on functional exercise capacity and respiratory performance of patients with COPD The main questions it aims to answer are
Is there difference in functional exercise capacity and respiratory performance without or with the use of elastic upper chest compression Is there difference in functional exercise capacity and respiratory performance between the use of elastic upper chest compression and elastic lower chest compression
Participants will
Be evaluated under three conditions on three different days without elastic compression with upper chest compression and with lower chest compression with the order of compression application randomly assigned
The functional capacity and respiratory muscle performance of all patients will be evaluated
The days for evaluation will be at least three days apart from each other
Is there difference in functional exercise capacity and respiratory performance without or with the use of elastic upper chest compression Is there difference in functional exercise capacity and respiratory performance between the use of elastic upper chest compression and elastic lower chest compression
Participants will
Be evaluated under three conditions on three different days without elastic compression with upper chest compression and with lower chest compression with the order of compression application randomly assigned
The functional capacity and respiratory muscle performance of all patients will be evaluated
The days for evaluation will be at least three days apart from each other
Detailed Description:
Participants will be evaluated under three conditions without elastic compression with upper chest compression and with lower chest compression with the order of compression application randomly assigned A Red Theraband will be used to apply compression to the upper and lower regions of the chest For a standardized approach to apply compression the top edge will be aligned with the 3rd intercostal space for the upper chest compression while the central horizontal part will line up with the xiphoid process of the sternum for the lower chest compression After exhaling to the EELV the circumferences of the upper and lower chest regions will be measured using the 3rd intercostal space as the measurement mark for the upper chest and the xiphoid process of the sternum as the measurement marks for the lower chest The Thera-Band will be adjusted to 90 of the measured circumferences ensuring it is securely fastened and standardized resistance is applied consistently to the thoracic regions of interest throughout the study After chest compression is applied participants will undergo measurements for functional exercise capacity and respiratory muscle performance
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None