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NCT03254225 Clinical Trial

Sixteen Weeks of Resistance Training in Hypertensive Elderly, Effects on Heart Rate Variability

Hypertension Clinical Trial

Official title:
Sixteen Weeks of Resistance Training in Hypertensive Elderly, Effects on Heart Rate Variability

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03254225
Other study ID # CEP1844640
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 4, 2018
Est. completion date April 30, 2021

Study information
Verified date March 2022
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the inffluence of 16 weeks of resistance training on heart rate variability of hypertensive elderlies patients. All volunteers will be divided in two groups, one will participate in a protocol of sixteen weeks of resistance training, an the other will remain sedentary.

Description:

This study evaluates the inffluence of 16 weeks of resistance training on heart rate variability using time and frequency-domains by ECG tracks. Will be assessed the blood pressure using the ambulatory blood pressure monitoring method of hypertensive elderly patients. All volunteers will be divided in two groups, one will participate in a protocol of sixteen weeks of resistance training prescribed with a relative workload of 50% of 1 maximal repetition, an the ontrol group will remain sedentary.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date April 30, 2021
Est. primary completion date January 30, 2020
Accepts healthy volunteers No
Gender All
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria: - Hypertensives - Age 60 to 80 years - Nonactive Exclusion Criteria: - Orthopedic problems or other problem that prevented the exercises - Change in drug treatment during protocol - Absence in more than 25% of the exercise sessions

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Resistance training
Resistance training performed three times at week for 16 weeks, in 8 exercises for the main muscles, the protocol of 3 sets of 10 repetitions with intensity of 50% of 1 maximum repetition (MR).

Locations
Country Name City State
Brazil Fabio Tanil Montrezol Santos Sao Paulo

Sponsors (2)
Lead Sponsor Collaborator
Federal University of São Paulo Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary Blood pressure change due to resistance training Blood pressure will be measured by Ambulatorial Monitoring Blood Pressure before and after 16 weeks of intervention. 16 weeks
Secondary Heart rate variability - Time domain - change due to resistance training Heart rate variability will be collected by electrocardiogram before and after 16 weeks of intervention 16 weeks
Secondary Heart rate variability - Frequency domain - change due to resistance training Heart rate variability will be collected by electrocardiogram before and after 16 weeks of intervention 16 weeks
Secondary Heart rate variability - Non-linear methods - change due to resistance training Heart rate variability will be collected by electrocardiogram before and after 16 weeks of intervention 16 weeks
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