CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 60 enrolled
Drug / intervention
Traditional Pilates group +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03791307
NCT03791307N/ACompleted
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Blood Pressure, Autonomic Heart Rate Modulation, Cardiorespiratory Parameters, Functionality and Quality of Life in Hypertensive Women After 16 Weeks of Training Based on the Pilates Method

João Luiz Q. Durigan·interventional·Posted Jan 2, 2019·Updated Mar 25, 2020

In Brief

A clinical study evaluating Traditional Pilates group and Modified Pilates group for Hypertension. Completed, enrolled 60 participants across 1 site.

Detailed Summary

The main objective of this study is to evaluate and compare the effect of the Pilates method associated with aerobic exercise and the traditional Pilates method on the blood pressure of hypertensive medicated women. In addition, we aim to analyze and compare the chronic effects of training on cardiac autonomic modulation, on cardiorespiratory fitness, functionality and quality of life.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHypertension
CountriesBrazil
CollaboratorsCatholic University of Brasília

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedJan 2, 2019
Enrollment StartApr 8, 2019
Primary CompletionDec 20, 2019
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 7.5 years ago

Interventions

Traditional Pilates groupother

The participants will perform only exercises based on the traditional Pilates method, 2 times a week, for 50 minutes, for 16 weeks.

Modified Pilates groupother

The participants will perform exercises based on the Pilates method alternated with active rest periods on treadmill ergometer, 2 times a week, for 50 minutes, for 16 weeks.