Study design and participants
This is an experimental study which evaluated cardiovascular parameters before and after a single supervised CR session. Furthermore, the association between the scores assessed in the quality-of-life questionnaire, Duke Activity Status Index (DASI) and Human Activity Profile (HAP) was verified.
The sample was taken by convenience, composed of patients of both sexes, aged 50 to 90 years, undergoing follow-up in a CR program for at least 6 months. The inclusion of patients was voluntary upon signing an Informed Consent Form. Patients with a diagnosis of arrhythmia, those using a cardiac pacemaker, and those who engaged in physical activity in the last 24 hours were excluded.
PROCEDURES
Experimental protocol
Weight and height were assessed, and the body mass index was calculated. Cardiovascular parameters were collected before and after the CR session. The questionnaires were applied before the cardiovascular measurements, always by the same researcher and with standardized speech. Information on medication use and comorbidities was collected from medical records.
Cardiovascular rehabilitation session
Each session lasted 60 minutes15. Participants warmed up for 15 minutes with dynamic exercises. Then, they performed another 15 minutes of dynamic exercises on a mat involving the large muscle groups of the lower limbs. The aerobic exercises lasted 30 minutes and were performed on a treadmill (LX160 Treadmill, Movement, Brazil) and horizontal bicycle (RT 230 Professional Training, Movement, Brazil). We standardized the bicycle as the last activity to be performed. Exercise intensity was low to moderate for patients who had performed the exercise test. The prescription for patients who started the program without a functional test was based on the modified subjective perception of exertion scale (Borg 0–10), ranging between 2 and 415,16.
Each session lasted 60 minutes. Participants began with a 15-minute warm-up consisting of dynamic exercises, such as circular movements of arms and shoulders, walking high kicks, and butt kicks. Following the warm-up, they performed 15 minutes of dynamic exercises on a mat that included at least four types of exercises targeting the large muscle groups of the lower extremities, such as bridges, mountain climbers, and knee-bent leg lifts. The aerobic exercises lasted 30 minutes and were performed on a treadmill (LX160 Treadmill, Movement, Brazil) and a horizontal bicycle (RT 230 Professional Training, Movement, Brazil), with the bicycle standardized as the final activity.
For participants who performed an exercise test, the intensity of the aerobic exercises was prescribed as low to moderate, based on heart rate ranges corresponding to 50–70% of heart rate reserve or Borg scale ratings of perceived exertion (RPE) between 2 and 4. For those who initiated the program without a functional test, the exercise intensity was determined using the modified Borg 0–10 scale, also ranging between 2 and 4. These parameters aimed to standardize the internal load and ensure a safe and effective intervention.
INSTRUMENTS
Cardiovascular parameters assessment
Cardiovascular parameters were evaluated using a Pulse Wave Analysis Monitor (Mobil-O-Graph®, IEM, Germany) in accordance with previous studies by our group17–19. This device uses the oscillometric method of evaluating brachial artery blood pressure for a non-invasive estimation of the central or aortic pulse wave. The central pulse wave provides the augmentation index corrected to 75 bpm (AIx@75) and the central vascular pressures [systolic blood pressure (cSBP), diastolic blood pressure (cDBP), pulse pressure (cPP) and mean arterial pressure (cMAP)]. The Alx@75 was evaluated from the aortic pulse wave through the difference in pressure between the peak of the reflection wave (P2) and the peak of the incident wave (P1), expressed as a percentage of the central pulse pressure (cPP) [AIx@75 = (P2-P1)/cPP x 100]. The ARCSolver method enables estimating PWV using a mathematical model, taking into account several parameters obtained by aortic pulse wave analysis and wave separation analysis20. Hemodynamic parameters [cardiac output (CO), total vascular resistance (RVT), cardiac index (CI)] and heart rate (HR) were also evaluated. Aortic pulsatility (cPP/cMAP) was analyzed from the hemodynamic parameters21.
The device carried out an evaluation of the quality of the records, where quality 1 means signal acquisition greater than 80%, 2 means signal acquisition greater than 50% and quality 3 and 4 records mean low quality and were not considered22. Three measurements were taken, and the average was considered for final analysis.
The Mobil-O-Graphy® cuff was selected based on the circumference of the participant’s left arm, positioned 2 cm from the cubital fossa of the left arm. Assessments were done by a single trained evaluator. The baseline measurement, meaning before exercise, was carried out with the patient in a sitting position, after 10 minutes of rest. The baseline measurement, meaning before exercise, was carried out with the patient in a sitting position, on a chair with the soles of both feet apart and resting on the floor, after 10 minutes of rest. The post-exercise measurement was performed in the same position immediately after exercise.
Quality of life assessment: Short-form Health Survey (SF-36)
The quality of life assessed using the Short-Form Health Survey (SF-36), a generic instrument which assesses the patient’s perception of health-related quality of life. This tool contains 36 items that encompass 8 domains involving physical and mental aspects: functional capacity (10 items); physical performance (4 items); pain (2 items); general health status (5 items); vitality (4 items); social aspects (2 items); emotional aspects (3 items) and mental health (5 items). The physical component assesses functional capacity, general clinical status, pain and physical appearance. The mental component encompasses aspects that refer to vitality, social issues, emotional issues and mental health assessment. The counts of the 36 questions are transformed into a scale of 0-100, where higher values indicate a better perception of health status23,24.
Assessment of physical activity level: HAP questionnaire
The physical activity level was assessed using the HAP questionnaire. This questionnaire consists of 94 items which assess the individual’s self-care, work, social activities and physical activity level classified according to the energy expenditure necessary to perform each task. The items are arranged in increasing order of energy expenditure, meaning that higher numbers correspond to greater energy expenditure. Respondents were asked to indicate whether they were “still doing this activity”, whether they had “stopped doing this activity” or had “never done this activity”. The HAP can be applied to individuals with different functional levels, from very low (getting up and sitting down from a chair or bed without assistance) to very high (running 4.8 kilometers), thus providing two scores: Maximum Activity Score (MAS) and Adjusted Activity Score (AAS)25,26. MAS is the number of the activity that presents the highest oxygen demand that the participant is still performing. The AAS is calculated from the MAS, which is the number of items that the individual “stopped doing” prior to the last one that he/she “still does” and is subtracted from the MAS. This latter score is considered a more stable estimate of the individual’s daily activity compared to the MAS. The AAS can be used to classify an individual’s general level of physical fitness and activity into three categories: inactive (score below 53), moderately active (score between 53 and 74), and active (score above 74)27,28.
Assessment of functional capacity: DASI questionnaire
Functional capacity was assessed using the DASI questionnaire, which was developed to evaluate patients with cardiovascular diseases29. It is a self-report questionnaire containing 12 questions that are based on activities of daily living29,30. Each questionnaire´s item presents a corresponding MET value of the task performed. Its score varies from 0 to 58.2 ml.kg− 1.min− 1, directly proportional to the individual’s functional capacity. The higher the score, the greater the functional capacity29.
Sample size calculation
The sample size was calculated with a computational software (G Power version 3.1.9.6)31 considering the AIx@75 values before and after physical exercise from a pilot study, with the effect being d = 0.34, significance level of 5% and power (beta) of 80%. The sample size calculation resulted in a final sample of 70 patients.
Statistical analysis
Numerical variables were described as central tendency (mean) and variability measures (SD), and categorical variables were described as absolute and relative frequencies. Data normality was assessed using the Kolmogorov-Smirnov test. For comparisons of variables before and after the intervention, the paired Student’s t-test or Wilcoxon test was used, when appropriate. For correlation analysis, Pearson’s correlation coefficient was used for parametric data or Spearman’s correlation coefficient for non-parametric data. The level of significance adopted in all tests was 5%. Data analysis was performed using the Prism 8 software program (GraphPad Software, Inc., San Diego, CA, USA).