Hypertension
Conditions
Interventions
The 12-week training was conducted at an outpatient clinic, in equipped and air conditioned room, with three weekly 1-hour sessions on alternate days. All participants were provided beforehand experie
• 2nd week: a volume adjustment was implemented and then the time determined for treadmill walking was 25 minutes, using Vcrit1
• 3rd week: a 30-minute treadmill treadmill was maintained at the same speed as the previous week
• 4th week: the training lasted 35 minutes with Vcrit1. On that occasion, a reassessment was made, based on the CF's to dete
Behavioural
E02.760.169.063.500.387
Sponsors
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Fundo de Apoio ao Ensino, à Pesquisa e à Extensão – FAEPEX, Universidade Estadual de Campinas – Unicamp
Eligibility
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: Participants who met the following inclusion criteria were considered eligible for inclusion in the study: hypertensive patients classified in stages 1, 2 and 3 (Stage 1: SBP between 140-159 mmHg and / or DBP between 90-99 mmHg; Stage 2: PAS between 160-179 mmHg and / or PAD between 100-109 mmHg and Stage 3: SBP ? 180mmHg and / or PAD ? 110 mmHg) according to the VI Brazilian Guidelines for SAH; patients rated with very weak and reasonable physical fitness according to American Heart Association criteria, which uses the maximum oxygen consumption (ml / kg / min) for classification.
Exclusion criteria
Exclusion criteria: Participants who presented one of the following conditions were: non-verbal communication; Grade III obesity, ie, Body Mass Index (BMI)> 40kg / m2; patients with a history of coronary disease classified as moderate to high risk (classes C and D) for physical training according to the American Heart Association criteria.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Increased heart rate variability (HRV) at rest, verified by means of the frequency meter, from the observation of a variation of at least 40% in the pre- and post-intervention measurements. 2. Increased functional capacity, verified by the peak oxygen consumption measured by the ergospirometric test; from the observation of a variation of at least 10% in the pre- and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Decreased blood pressure levels, verified by means of blood pressure measurement obtained by the sphygmomanometer, from the observation of any reduction in pre and post-intervention measurements. | — |
Countries
Brazil
Contacts
Public ContactThaís São João
Universidade Estadual de Campinas
Outcome results
None listed