Ignite Creation Date:
2024-05-06 @ 7:11 PM
Last Modification Date:
2024-10-26 @ 3:02 PM
Study NCT ID:
NCT05923580
Status:
RECRUITING
Last Update Posted:
2024-05-08
First Post:
2023-06-05
Brief Title:
Group-based Cardiac Telerehabilitation and Its Effectiveness
Sponsor:
University of Eastern Finland
Organization:
University of Eastern Finland
Study Overview
Official Title:
Group-based Cardiac Telerehabilitation and Its Effectiveness
Status:
RECRUITING
Status Verified Date:
2024-05
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:
Cardiovascular diseases CVD and coronary artery diseases CAD are the most common cause of death worldwide After an acute cardiac event prevention of new cardiac events is essential and reduces suffering Group-based cardiac telerehabilitation CTR refers to the use of information and communication technologies for rehabilitation purposes in promoting CAD patients health
Detailed Description:
This study aims to assess the group-based cardiac telerehabilitation model and its effectiveness The data is collected from two University hospitals in Finland Patients with coronary heart disease two months after percutaneous coronary intervention N198 are invited to the study All the participants are being treated in a healthcare unit that uses digital care pathways for coronary patients Patients can choose the usual care or group-based cardiac telerehabilitation as follow-up care All the patients are invited to the study after the chosen follow-up care telerehabilitation or usual care Patients will be allocated into two groups The telerehabilitation group is the intervention group and the usual care group is the control group Quality of life adherence to treatment and lifestyle changes are measured at the baseline and 3 6 and 12 after the intervention baseline
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