Hypertension
Conditions
Interventions
The intervention consisted of three groups: two treatment groups (combined training in series and combined training in circuit) and one group without treatment (control), as shown below.
1) Control Gr
and did not participate in the supervised physical exercises proposed by the intervention
2) Combined Physical Training Group in Circuit: was composed of 10 volunteers who received medications and information for the treatment of hypertension, according to the procedures of the Basic Healt
and resisted exercises: Multiexercise (sitting supine, high pull, shoulder development, and knee extension), Rowing, Diagonal Rotation, Surfing and Legpress (leg press and plantar flexion). The exerci
and at each turn 10 to 30 repetitions were made for each resistance exercise. The aerobic part comprised twenty minutes, divided in four sessions of five minutes, that was realized before each turn of
e
3) Combined Physical Training Group was composed of 10 volunteers who received medications and information for the treatment of hypertension, according to the procedures of the Basic Health Unit, a
Other
I02.233.543
Sponsors
Universidade Metodista de Piracicaba - UNIMEP
Universidade Federal de Mato Grosso do Sul (UFMS) - Campus Pantanal
Eligibility
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria were considered: both genders; age between 40 and 70 years; be hypertensive, according to the VII Arterial Hypertension Guideline (SBC, 2016); have clinical stability, as assessed by the cardiologist and / or clinician and medical certificate for participation in the study.
Exclusion criteria
Exclusion criteria: The exclusion criteria adopted were: to have diabetes and heart diseases; chronic obstructive pulmonary disease and asthma; obesity grade III; musculoskeletal and / or neuromuscular changes, which make it impossible to perform the tests and physical training; some other clinical condition diagnosed after the mandatory exams for inclusion in the program; participation in physical training programs, at the time of screening, in the last six months, and during the study; and absence in three consecutive classes in the training program.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body Mass Index (BMI): it was determined by the relationship between body mass (BM) in kilograms and the square of height (H), in meters (BM/H2), before and after 16 weeks of intervention. It was used an anthropometric digital scale of the Welmy brand (Santa Bárbara d 'Oeste, São Paulo, Brazil).;Incremental Shuttle Walking Test (ISWT): a progressive loading test, before and after 16 weeks of intervention, was used to evaluate the functional capacity, by means of the distance traveled, in a corridor with 10 meters in length, and obeying to the sound signal, programmed by a software, which indicates the moment to start the next turn. The test consists of 12 stages, with a successive increase of 1 lap at each stage, totaling 14 laps. As the test progresses, the interval between the beeps decreases, increases the number of laps and the speed of the walk. The test is finished if the volunteer does not reach the end of the runner before the sound signal, in a second attempt, and record the distance traveled from the number of complete laps.After two attempts, the highest number of laps performed was recorded.;6-Minute Walk Test (6MWT) The test was performed, before and after 16 weeks of intervention, in a corridor 30 meters long and 3 meters wide. The volunteers were instructed to walk for six minutes, without jogging or running, and according to their effort, being able to stop, slow down or rest in order to complete the walk without stopping time on the clock. The scores obtained in the 6MWT were used in the evaluation of cardiorespiratory capacity: VO2 (mL x min-1x kg-1) = -2.863 + (0.0563 x distance covered in the test). After two attempts, the highest number of laps performed was recorded.;The measures of circumference (cm) were determined with a flexible and inextensible measuring tape, with the volunteers in the orthostatic position, with the arms along the body and the uniformly distributed weight, before and after 16 weeks of intervention. Abdominal circumferenc | — |
Secondary
| Measure | Time frame |
|---|---|
| Acute effect of the physical training program was determined by the measurement of SBP, DBP and HR, for each volunteer at minutes 0, 10, 20, 30, 40, 50 and 60, in the first session after the period of familiarization of the training. | — |
Countries
Brazil
Contacts
Public ContactEli Pazziaotto Forti
Universidade Metodista de Piracicaba - UNIMEP
Outcome results
None listed