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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

The Effectiveness of a Physical Exercise Program in the Person Undergoing Cardiac Surgery

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07153874
Acronym
HeartBack2Beat
Enrollment
76
Registered
2025-09-04
Start date
2024-02-19
Completion date
2025-08-31
Last updated
2025-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery, Functional Status, Quality of Life, Rehabilitation Program

Brief 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.

Interventions

OTHERPhysical exercise rehabilitation intervention

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

Sponsors

Universidade Católica Portuguesa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
FunctionalityThe results are expected to be measured at the beginning of the program, at six weeks, and at the end (at 12 weeks).Functionality is the ability regarding basic physical and cognitive activities such as walking or reaching, focusing attention, and communicating, as well as the routine activities of daily living, including eating, bathing, dressing, transferring, and toileting; and life situations such as school or play for children and, for adults, work outside the home or maintaining a household. It will be measured by the London Chest Daily Activities scale.
Perceived Quality of lifeThe results are expected to be measured at the beginning of the program, at six weeks, and at the end (at 12 weeks).Quality of life is a generic concept reflecting concern with the modification and enhancement of life attributes, e.g., physical, political, moral, social environment as well as health and disease. It will be measured by the Short Form-36 quality of life assessment scale.
Tolerance to physical exerciseThe results are expected to be measured at the beginning of the program, at six weeks, and at the end (at 12 weeks).Tolerance to physical exercise is the exercise capacity of an individual as measured by endurance (maximal exercise duration and/or maximal attained work load) during an exercise test. It will be measured by the 6-minute walk test.

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026