Clinical Trials in Brazil / NCT04126785
Recruiting Not applicable

High-Intensity Interval Versus Moderate-Intensity Continuous Water Based Exercise in Hypertensive Older Individuals

NCT04126785 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2019-11-01
Last updated
2025-07-25

Condition(s) studied

Hypertension

Investigational drug(s) / intervention(s)

High Intensity Interval Exercise in Heated Water-BasedContinuous Moderate Exercise in Heated Water-BasedControl Group

High Intensity Interval Exercise in Heated Water-Based: High intensity interval exercise will perform at controlled heated water-base (30 e 32 ºC). Subject will be submerged at the xiphoid process level. The session will consist in 4 min walking (warm-up) at 9 level of rate perceived exertion (RPE) scale, followed by 21 min of HIIE, alternating 1 min of jogging/running at 15-17 (hard-very hard) level with 2 min of walking at 9-11 (very light-fairly light) level of RPE.

Continuous Moderate Exercise in Heated Water-Based: Continuous moderate exercise will perform at controlled heated water-base (30 e 32 ºC). Subject will be submerged at the xiphoid process level. The session will consist in 4 min walking (warm-up) at 9 level (light) of RPE, followed by 26 min of MICE, walking at 11-13 (fairly light)level of RPE.

Control Group: CON session will perform at controlled heated water-base (30 e 32 ºC). Subject will be seated in a chair and submerged at the until xiphoid process level for 30 min.

Study summary

This study will investigate the acute and chronic effects in hemodynamic and autonomic variables to high-intensity interval versus moderate-intensity continuous heated water-based exercise in older individuals with hypertension.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * ≥60 years old; * Hypertension diagnosed at least 6 months earlier (stage 1 or 2); * Antihypertensive drug treatment and without dosage alteration at least 3 months earlier; * Blood pressure inferior to 140/90 mmHg in medical office. Non-inclusion criteria: * Smoking individuals; * Uncontrolled cardiovascular disease; * Disability; * Deficit cognitive; Exclusion Criteria: * Non 100% participation; * Change (or stopped) clinical or drug treatment.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
São Paulo State Univeristy Bauru São Paulo Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04126785 on ClinicalTrials.gov ↗ ← All trials in Brazil