Ignite Creation Date:
2024-10-26 @ 3:38 PM
Last Modification Date:
2024-10-26 @ 3:38 PM
Study NCT ID:
NCT06563882
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-05-04
Brief Title:
Postural Management of Hyperkyphosis in Cardiac Rehab Patients
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Postural Management of Hyperkyphosis to Improve Motor Performance and Pulmonary Function in Cardiac Rehabilitation Patients
Status:
RECRUITING
Status Verified Date:
2024-08
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 evaluate the efficacy of a home-based exercise program in managing hyperkyphosis and its impact on physical performance and pulmonary function among cardiac rehabilitation patients
The primary research question is Can a home-based kyphosis-specific exercise program reduce thoracic hyperkyphosis and improve physical ability in cardiac patients undergoing cardiac rehabilitation The study will consist of three groups 1 Hyperkyphotic participants undergoing a 12-week exercise program at home alongside a cardiac rehabilitation exercise program 2 Hyperkyphotic participants solely undergoing cardiac rehabilitation exercise program and 3 Participants without hyperkyphosis solely undergoing cardiac rehabilitation exercise program
The groups will be evaluated based on measurements of kyphosis index physical performance and spirometry at the beginning after 6 weeks and upon completion of the 12-week program
The primary research question is Can a home-based kyphosis-specific exercise program reduce thoracic hyperkyphosis and improve physical ability in cardiac patients undergoing cardiac rehabilitation The study will consist of three groups 1 Hyperkyphotic participants undergoing a 12-week exercise program at home alongside a cardiac rehabilitation exercise program 2 Hyperkyphotic participants solely undergoing cardiac rehabilitation exercise program and 3 Participants without hyperkyphosis solely undergoing cardiac rehabilitation exercise program
The groups will be evaluated based on measurements of kyphosis index physical performance and spirometry at the beginning after 6 weeks and upon completion of the 12-week program
Detailed Description:
None
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