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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06370546
Other study ID # 229/2022
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 20, 2023
Est. completion date July 20, 2024

Study information

Verified date May 2024
Source Universidad Católica del Maule
Contact Luis Benavides-Roca, MSc
Phone +56 9 9926 8137
Email benavides.roca@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to determine the acute effects of high and low-intensity strength training on cardiac autonomic control in hypertensive subjects


Description:

The present study aims to determine the cardiovascular response in hypertensive individuals between 30 and 60 years old to one session of high and low intensity strength training. Participants will undergo a low-intensity strength training including squats, barbell rows, deadlifts and chest presses with a load dynamic of 12 repetitions for 6 sets at an execution speed of less than 55 % of your maximum weight. This is followed by a one-week washout period. Subsequently, high intensity strength training is performed with the same exercises but with a load of 6 repetitions for 6 series at an intensity greater than 80% of the maximum repetition speed. The order of the sessions will be random. After each session, blood pressure will be recorded for 24 hours using a holter monitor, which will report pressures during both day and night The results obtained will be determined by the differences in the before and after values. Consequently, the behavior of the following variables: 1) heart rate variability, 2) blood pressure and 3) heart rate will determine the final results of this research. The entire study will be carried out at the Catholic University of Maule, in its Kinesiology laboratory.


Recruitment information / eligibility

Status Recruiting
Enrollment 28
Est. completion date July 20, 2024
Est. primary completion date July 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: - Participants exclusively diagnosed with hypertension by a medical professional Exclusion Criteria: - Participants with any other chronic medical condition - Subjects with any upper or lower limb injury that prevents strength training - Subjects with cardiovascular abnormalities other than hypertension

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Low intensity
Low intensity group: participants will be requested to perform the following exercises: 1)squat, 2) rowing, 3)deadlift and 4)bench press. All exercises will be performed with low intensity (55% of the maximum velocity used in one-repetition maximum) and will be supervised by a researcher.
high intensity
High intensity group: participants will be requested to perform the following exercises: 1)squat, 2)rowing, 3)deadlift and 4)bench press. All exercises will be performed with high intensity (80% of the maximum velocity used in one-repetition maximum) and will be supervised by a researcher.

Locations

Country Name City State
Chile Universidad Católica del Maule Talca Maule

Sponsors (1)

Lead Sponsor Collaborator
Universidad Católica del Maule

Country where clinical trial is conducted

Chile, 

Outcome

Type Measure Description Time frame Safety issue
Primary Heart rate variability Determine the effects of high and low-intensity strength training on heart rate variability, based on the time between each heartbeat, during the assessment 2 hours
Primary Blood pressure systolic Determine the effects of high and low intensity resistance training on blood pressure with a blood pressure monitor for 24 hours. 24 hours
Primary Blood pressure diastolic Determine the effects of high and low intensity resistance training on blood pressure diastolic with a blood pressure monitor for 24 hours. 24 hours
Primary Blood pressure mean Determine the effects of high and low intensity resistance training on blood pressure mean with a blood pressure monitor for 24 hours. 24 hours
Primary Heart Rate Determine the effects of high and low intensity strength training on the behavior of heart rate, using a heart rate monitor, throughout the intervention. 24 hours
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