Arterial Hypertension Clinical Trial
Official title:
The Influence of Regular Aerobic Interval Training on Blood Pressure and Arterial Stiffness Amongst Hypertensive Subjects
Regular exercise is recommended as an adjuvant treatment in hypertensive subjects by both European and American guidelines. Crucially, however, there are no precise recommendations on the type of physical exercise and how it should be instituted A relatively short period (5 months) of regular aerobic interval training (AIT), significantly decreased blood pressure, pulse wave velocity, and most applanation tonometry indexes in hypertensive subjects also undertaking pharmacological treatment in our study.
Regular physical exercise appears to potentiate the effects of pharmacological treatment for
arterial hypertension. As such, regular exercise is recommended as an adjuvant treatment in
hypertensive subjects by both European and American guidelines. Crucially, however, there
are no precise recommendations on the type of physical exercise and how it should be
instituted. Aerobic Interval Training (AIT) is a new and novel type training that appears to
be beneficial to patients suffering from various medical conditions. There is a distinct
lack of evidence on how it affects arterial hypertension. The aim of this study was to
evaluate the influence of a 5 month period of regular AIT on blood pressure, carotid femoral
pulse wave velocity (PWV) and applanation tonometry indexes in patients previously treated
pharmacologically for mild or moderate arterial hypertension.
The study group consisted of 60 hypertensive subjects (30 males, 30 females) (age 54.45 ±
8.52 years) who had previously undergone at least 2 years of combined anti-hypertensive
therapy and who had well controlled hypertension, i.e. below 140/90 mmHg. Their
pharmacological treatment did not change during the study period. The study group was
randomly divided into 2 subgroups. In the first group (G1), AIT was undertaken for 5 months
(40 professional AIT sessions performed two times per week in 50 minute sessions) and
followed a specially developed program. The second control group (G2), did not attend any
training sessions but received medical advice on how to maintain physical activity as
outlined by JNC (Joint National Committee) hypertension guidelines. During the baseline
visit and then at five months (final visit), both groups underwent testing for office BP
(blood pressure), PWV and applanation tonometry indexes using the SphygmoCor® device and the
Complior® device.
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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