Cardiovascular Diseases, Cardiovascular Risk Factor
Conditions
Keywords
Rehabilitation Service, Signals and symptons, Heart Rate, Blood pressure, Respiratory Muscles, autonomic modulation, exercise, risk measurement, muscle strength, inflammation, cytosines
Brief summary
Introduction: Despite the various beneficial effects, cardiovascular rehabilitation programs (CVRP) have been associated with the appearance of signs and symptoms. Risk stratification protocols are used to stratify into risk trials for an occurrence of events during physical exercise, although studies investigating their efficacy in predicting signs and symptoms during VCTV are inconclusive. In addition, several clinical, physical and biochemical parameters have been used in the literature as risk markers for the appearance of adverse events, and to investigate whether these parameters are capable of predicting a possibility of intercurrences during PRCV sessions.Objectives: 1) to evaluate the efficacy of risk stratification protocols in predicting signs and symptoms during the performance of a PRCV; 2) to analyze the correlation between clinical, physical and biochemical parameters measured at rest with the presence of signs / symptoms in participants of a PRCV; 3) to evaluate whether changes in clinical, physical or biochemical parameters induced by PRCV influence the appearance of signs and symptoms during PRCV. Materials and Methods: To perform this study, data from 70 patients inserted in a PRCV will be evaluated. The study will be divided into three subprojects that can be divided into three stages: 1) risk stratification of patients who will participate in the study by two independent evaluators (Study 1) and evaluation of clinical parameters (cardiorespiratory parameters and autonomic modulation evaluation); (maximal isometric resistance, maximal isometric contraction, functional capacity and level of physical activity) and biochemical (IL-6, TNF-alpha and IL-10) (Studies 2 and 3). Patients will then be followed up by 24 sessions during the PRCV routines to evaluate signs and symptoms, for posterior correlation with the risk stratification obtained in each protocol (Study 1), and with resting values of clinical, physical and biochemical studies (Studies 2 and 3); 2) Patients perform the normal routines of their PRCV for a period of 6 months (Study 3); 3) The patients will again have their clinical, physical and biochemical parameters evaluated and then will be followed up for another 2 months (24 sessions) during the routines of the PRCV sessions to evaluate signs and symptoms, which will allow to evaluate if gains / losses in these parameters exert influence on the appearance of signs and symptoms during PRCV sessions.
Interventions
The cardiovascular rehabilitation program is performed three times weekly on alternate days and each session lasts approximately 60 minutes divided as follows: 5 minutes to the initial rest where blood pressure (BP), heart rate (HR) and signs and symptoms are assessed; 15 minutes of warm-up, composed by global stretches, lower and upper limb exercises, and exercises combining the two modes; then, patients go to the resistance phase (30 minutes), where are performed an individualized aerobic protocol according to their HR reserve values using bicycle and treadmill (at the 4th and 10th minute of both ergometers at HR is evaluated, and in the bicycle is also evaluated the BP of all the patients). The end of the protocol is composed of 10-minute relaxation, during which the patients perform a small cardiovascular deceleration (a few laps around the room, with free speed) and, finally, lie down at rest. The presence of signs and symptoms is assessed at all stages of the program.
Sponsors
Fundação de Amparo à Pesquisa do Estado de São Paulo
Universidade Estadual Paulista Júlio de Mesquita Filho
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
Yes
Inclusion criteria
* To present clinical diagnosis of cardiovascular disease and/or cardiovascular risk factors; * Be able to perform all the proposed evaluations; * Agree to participate in the studies.
Exclusion criteria
* Patients who miss more than six consecutive sessions of the program or those who total more than 12 absences during the two months that total the period of analysis of the signs and symptoms will be excluded from the analyzes.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cardiovascular symptoms | 6 months | Symptoms like dizziness, angina pectoris, cramp, muscle pain, fatigue, nausea will be related for the volunteers, and the presence or absence will be registered. |
| Cardiovascular risk stratification protocols | 2 months | The cardiovascular risk stratification will be evaluated by seven diferent protocols and the volunteers will be stratified like less, medium and high cardiovascular risk. There will be used protocols of the organizations below: American College of Sports Medicine, Sociedade Brasileira de Cardiologia, American Heart Association, Frederic J. Pashkow protocol, American Association of Cardiovascular and Pulmonary Rehabilitation, Société Française de Cardiologie and Sociedad Española de Cardiología |
| Cardiovascular signals | 6 months | Signals like pulse rate changes, increased SBP and DBP during exercise, tachipnea, pallor will be observed by the evaluator and the presence or absence will be registered. |
| Autonomic modulation | 6 months | The autonomic modulation will be evaluated by heart rate variability method |
| Blood pressure | 6 months | The blood pressure will be evaluated with a non invasive method |
| Heart rate | 6 months | The heart rate will be evaluated with an pulse oximeter with the volunteers at rest |
| Spirometric parameters | 6 months | The spirometric parameters will be evaluated by spirometry method. |
| Maximum expiratory and inspiratory pressure | 6 months | The maximum expiratory and inspiratory pressure will be evaluated by manovacuometry method. |
| maximum isometric muncle strength | 6 months | The vollunteers will realize the maximum isometric strength with a dominant member during 5 seconds, and the maximum value obtained will be registered. |
| voluntary isometric contraction | 6 months | The volunteers will do a maximum voluntary isometric contraction and instructed to maintain this contraction as longer they can. The maximum time obtained will be registered. |
| Cardiorrespiratory fitness | 6 months | The vollunters will be submited to a maximum effort test to define their cardiorrespiratory fitness. |
| Physical activity level | 6 months. | The physical activity of the volunteers will be registered during one week to determine their physical activity level. |
| Biochemical parameters | 6 months | Inflamatory (TNF-alpha, IL-6) and anti-inflamatory cytokines (IL-10) will be analysed by blood samples. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Respiratory frequency | 6 months | The respiratory parameters respiratory frequency will the evaluated by number of tract per minute with the volunteers at rest. |
| oxygen saturation | 6 months | The respiratory parameter oxigen saturation of the volunteers will be evaluated with a pulse oximeter with the volunteers at rest. |
Contacts
Primary ContactLuiz Carlos M Vanderlei, PhD
Backup ContactLaís M Vanzella, MD
Outcome results
None listed