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Clinical Trials in Portugal / NCT07153874
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The Research Aims to Study the Effectiveness of a Physical Exercise Program on Indicators of Quality of Life and Functionality: It Will be Applied at Home to People Undergoing Cardiac Surgery, in Phase II of Cardiac Rehabilitation

NCT07153874 · tracked via the Priya Life Science Portugal tracker
Sponsor
Universidade Católica Portuguesa
Phase
Not applicable
Started
2024-02-19
Last updated
2025-09-04

Condition(s) studied

Cardiac SurgeryRehabilitation ProgramQuality of LifeFunctional Status

Investigational drug(s) / intervention(s)

Physical exercise rehabilitation intervention

Physical exercise rehabilitation intervention: 12 weeks of physical exercise intervention, including aerobic snd anaerobic exercise at home. 36 sessions of monitorized training with distance supervision.

Study summary

The goal of this clinical trial is to test the effectiveness of an physical exercise intervention in people after cardiac surgery, namely valve replacement and coronary artery bypass graft. The main question\[s\] it aims to answer are: • what is the influence of a physical exercise program on quality of life in people after cardiac surgery • what is the influence of a physical exercise program on functional status in people after cardiac surgery. Participants will be allocated to exepriemtal group and perform a physical exercise program during 12 weeks and the program is composed by aerobic and anaerobic exercise. They will be evaluated at the beginning, middle and in the end of the program. Researchers will compare the experimental and the control group to see the effects in quality of life and functional status.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
* Clients undergoing cardiac surgery for the first time: heart valve surgery, coronary artery bypass grafting, after discharge from hospital in a home setting; * Clients at low and moderate risk of cardiovascular events; * Clients over the age of 18; * Clients who are part of the localities assisted by the hospital unit; * Clients with preserved cognitive capacity.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centro Hospitalar Universitário de São João Porto Porto District

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07153874 on ClinicalTrials.gov ↗ ← All trials in Portugal