Cardiovascular Diseases Clinical Trial
Official title:
Application of Exercises Based on the Pilates Method on the Functional Capacity in Postoperative Surgery Coronery Artery Bypass Grafting: Randomized Clinical Trial
The major cause of mortality worldwide is due to cardiovascular diseases. A way to treat
these diseases is coronary artery bypass grafting, one of the most common surgical
procedures in the world. The incidence of post-operative complications contributes to
functional decline of the patient, reduced quality of life and post-discharge mortality.
Also, cardiac surgery leads to changes in lung capacity and respiratory muscle strength,
causing a decrease in the function lung. Physical therapy proves to be an effective tool to
combat changes resulting from cardiac surgery, demonstrating beneficial results in the
pulmonary function, functional capacity, and peripheral and respiratory muscle strength. The
Pilates method has been studied as a therapeutic way to healthy subjects and various kinds
of diseases, but there are no studies in the literature evaluating the effect method in
patients after coronary artery bypass surgery.
The aim of this study is to investigate the effect of Pilates on functional capacity , flows
and lung volumes, respiratory and peripheral muscle strength after coronary artery bypass
grafting.
Randomized clinical trial in which patients will be eligible after elective coronary artery
bypass surgery, randomly allocated into two groups : conventional physiotherapy group (n =
15) and Pilates method associated with conventional physiotherapy group (n = 15). The
outcomes will be assessed by blinded evaluator and data randomization will be performed
through by electronic randomization.The interventions will take place during the length of
stay in the hospital, totalizing a maximum of six days of intervention.
It is expected that the application of the Pilates method exercise method associated with
conventional physiotherapy in patients in postoperative coronary artery bypass grafting
improves functional capacity, flows and lung volumes and respiratory and peripheral muscle
strength.
The exercise program will be held during the period of hospitalization for six days, often
two to three sessions per day, totaling 12 sessions. The intervention will start on the
first day postoperatively. The program may not exceed 30% of maximum heart rate reserve of
the patient that will be calculated by the Karvonen formula (Karvonen, Kentala et al.,
1957). The exercises will be conducted at the patient's bedside, using light resistance
springs representing the lowest possible burden of springs to be used in the Pilates method.
The exercises will be performed on the upper limbs alternating between the left and right
upper limb and likewise would run with the lower limbs by means of a protocol consists of
four exercises until the limit of resistance of the patient or interrupt pre-established
criteria.
One set of each exercise with a range of up to two minutes between exercises will be held.
In the first three days of intervention 10 repetitions of each exercise and the remaining
three days a total of 15 repetitions of each movement will be performed.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05654272 -
Development of CIRC Technologies
|
||
| Recruiting |
NCT05650307 -
CV Imaging of Metabolic Interventions
|
||
| Recruiting |
NCT04515303 -
Digital Intervention Participation in DASH
|
||
| Completed |
NCT04056208 -
Pistachios Blood Sugar Control, Heart and Gut Health
|
Phase 2 | |
| Recruiting |
NCT04417387 -
The Genetics and Vascular Health Check Study (GENVASC) Aims to Help Determine Whether Gathering Genetic Information Can Improve the Prediction of Risk of Coronary Artery Disease (CAD)
|
||
| Not yet recruiting |
NCT06211361 -
Cardiac Rehabilitation Program in Patients With Cardiovascular Disease
|
N/A | |
| Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
| Recruiting |
NCT04514445 -
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
|
||
| Enrolling by invitation |
NCT04253054 -
Chinese Multi-provincial Cohort Study-Beijing Project
|
||
| Completed |
NCT03273972 -
INvestigating the Lowest Threshold of Vascular bENefits From LDL Lowering With a PCSK9 InhibiTor in healthY Volunteers
|
N/A | |
| Completed |
NCT03680638 -
The Effect of Antioxidants on Skin Blood Flow During Local Heating
|
Phase 1 | |
| Recruiting |
NCT04843891 -
Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis.
|
Phase 1 | |
| Completed |
NCT04083872 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of Highdose CKD-385 in Healthy Volunteers(Fasting)
|
Phase 1 | |
| Completed |
NCT04083846 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers(Fed)
|
Phase 1 | |
| Completed |
NCT03466333 -
Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia
|
Phase 2 | |
| Completed |
NCT03619148 -
The Incidence of Respiratory Symptoms Associated With the Use of HFNO
|
N/A | |
| Completed |
NCT03693365 -
Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial
|
||
| Completed |
NCT04082585 -
Total Health Improvement Program Research Project
|
||
| Completed |
NCT05132998 -
Impact of a Comprehensive Cardiac Rehabilitation Program Framework Among High Cardiovascular Risk Cancer Survivors
|
N/A | |
| Completed |
NCT05067114 -
Solutions for Atrial Fibrillation Edvocacy (SAFE)
|