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Clinical Trials/NCT02670681
NCT02670681
Unknown
Not Applicable

Effects of Different Intensities of Aerobic Exercise on Blood Pressure Levels of Resistant Hypertensive Subjects

Federal University of Paraíba1 site in 1 country100 target enrollmentNovember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Federal University of Paraíba
Enrollment
100
Locations
1
Primary Endpoint
Systolic, diastolic and media blood pressure
Last Updated
7 years ago

Overview

Brief Summary

The aim of this intervention study is to evaluate the acute and chronic effects of different intensity (mild, moderate and high intensity) of aerobic exercise on blood pressure levels of subjects classified as resistant hypertension. Resistant hypertensives subjects aged 40 to 70, men or women with body mass index lower that 40 kg/m² are recruited and subjected in acute phase in three sessions of aerobic exercise: mild, moderate, high intensity; and session control. After, the subjects will be randomly allocated into four intervention groups: mild intensity group, moderate intensity group, high intensity group and control group. In both phases, the subjects have blood pressure data recorded by ambulatory blood pressure monitoring, for clinic and ambulatory analysis. In addition, continuously be registered biological signs of blood pressure (finometer), electrocardiogram (DII derivation) and blood flow (venous occlusion plethysmography) for analysis of cardiac autonomic modulation, vascular autonomic modulation, baroreflex sensitivity, vasodilator response and peripheral vascular resistance.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
March 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Federal University of Paraíba
Responsible Party
Principal Investigator
Principal Investigator

Leone Severino do Nascimento

Leone Severino do Nascimento, Universidade Federal da Paraíba

Federal University of Paraíba

Eligibility Criteria

Inclusion Criteria

  • Age between 40 and 70 years
  • Men or women
  • Body mass index under 40 kg / m²
  • Able to participate in exercise
  • No regular physically active in the last 4 months

Exclusion Criteria

  • Smoking; with history of ischemic stroke or hemorrhagic; or coronary heart disease; or obstructive pulmonary disease or chronic restrictive; or diabetes mellitus; or chronic atrial fibrillation.

Outcomes

Primary Outcomes

Systolic, diastolic and media blood pressure

Time Frame: Pre and post-intervention (8 weeks)

Control in blood pressure levels, assess by the method of Ambulatory Blood Pressure Monitoring (ABPM), from decrease of blood pressure in measurements pre and post-intervention with physical exercise.

Secondary Outcomes

  • Autonomic Modulation(Pre and post-intervention (8 weeks))
  • Baroreflex Sensitivity(Pre and post-intervention (8 weeks))
  • Vasodilator Response(Pre and post-intervention (8 weeks))

Study Sites (1)

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