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

F

Federal University of São Paulo

Status

Completed

Conditions

Hypertension

Treatments

Behavioral: Resistance training

Study type

Interventional

Funder types

Other

Identifiers

NCT03254225
CEP1844640

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 patients

Sex

All

Ages

60 to 80 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Resistance training
Experimental group
Description:
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).
Treatment:
Behavioral: Resistance training
Control
No Intervention group
Description:
in this arm, the group will remain sedentary for the same period of the experimental group, and they will be invited to engage on the raining program after the sedentary period

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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