- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06370546
Cardiac Response to Strength Training in Hypertensive Individuals
Evaluation of Cardiac Response to High and Low-Intensity Strength Training in Hypertensive Subjects
Study Overview
Status
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Maule Region
-
Talca, Maule Region, Chile, 3469001
- Universidad Católica del Maule
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: high intensity
The low-intensity group undergoes a strength training program using barbells, weights and dumbbells consisting of 6 sets of 6 repetitions each, with an execution speed equal to or greater than 80% of the maximum velocity used in the one-repetition maximum
|
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.
|
|
Experimental: Low Intensity
The low-intensity group undergoes a strength training program using barbells, weights and dumbbells, consisting of 6 sets of 12 repetitions each, with an execution speed below 40% of the maximum velocity used in the one-repetition maximum
|
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 (40% of the maximum velocity used in one-repetition maximum) and will be supervised by a researcher.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate variability
Time Frame: 2 hours
|
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
|
|
Blood pressure systolic
Time Frame: 24 hours
|
Determine the effects of high and low intensity resistance training on blood pressure with a blood pressure monitor for 24 hours.
|
24 hours
|
|
Blood pressure diastolic
Time Frame: 24 hours
|
Determine the effects of high and low intensity resistance training on blood pressure diastolic with a blood pressure monitor for 24 hours.
|
24 hours
|
|
Blood pressure mean
Time Frame: 24 hours
|
Determine the effects of high and low intensity resistance training on blood pressure mean with a blood pressure monitor for 24 hours.
|
24 hours
|
|
Heart Rate
Time Frame: 24 hours
|
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
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 229/2022
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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