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Effects of a Resistance Training Period on Blood Pressure of Hypertensive Elderlies: Influence of the Polymorphism of the Angiotensin Converting Enzyme

Effects of a Resistance Training Period on Blood Pressure of Hypertensive Elderlies: Influence of the Polymorphism of the Angiotensin Converting Enzyme

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01963507
Enrollment
136
Registered
2013-10-16
Start date
2010-04-30
Completion date
2013-04-30
Last updated
2013-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Brief summary

The study aimed to evaluate the chronic effects of resistance training on blood pressure and biochemical exams in hypertensive elderlies and the influence of the polymorphism of the angiotensin converting enzyme in these response.

Detailed description

To investigate the chronic effects of resistance training on blood pressure and biochemical exams in elderly, 135 hypertensive elderlies were divided into 2 groups: trained and control. The trained group was submitted to a resistance training period. Before the 16 weeks ACE gene was genotyped (PCR). Before and after 16 weeks, blood pressure (ambulatory), HDL-cholesterol, Total cholesterol, Glycemia, Triacylglycerol (colorimetric assay) and plasminogen activator inhibition (PAI-1), intercellular adhesion molecule (ICAM-1), vascular endothelial cell adhesion molecule (VCAM-1), Adiponectin, tumor necrosis factor alpha (TNF-alpha), C Reactive Protein, Angiotensin II, Angiotensin Converting Enzyme, Angiotensin 1-7, (ELISA assay) were measured.

Interventions

BEHAVIORALResistance 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).

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
Federal University of São Paulo
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Hypertensives * Age 60 to 85 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

Design outcomes

Primary

MeasureTime frameDescription
Blood Pressure16 weeksBlood pressure was measured by Ambulatorial Monitoring Blood Pressure before and after 16 weeks of intervention.

Secondary

MeasureTime frameDescription
VCAM-116 weeksVCAM-1 was analyzed by ELISA assay, before and after 16 weeks of intervention.
HDL-cholesterol16 weeksHDL-cholesterol was analyzed by colorimetric assay, before and after 16 weeks of intervention.
Total Cholesterol16 weeksTotal cholesterol was analyzed by colorimetric assay, before and after 16 weeks of intervention.
Glycemia16 weeksGlycemia was analyzed by colorimetric assay, before and after 16 weeks of intervention.
Triacylglycerol16 weeksTriacylglycerol was analyzed by colorimetric assay, before and after 16 weeks of intervention.
PAI-116 weeksPAI-1 was analyzed by ELISA assay, before and after 16 weeks of intervention.
ICAM-116 weeksICAM-1 was analyzed by ELISA assay, before and after 16 weeks of intervention.
TNF alpha16 weeksTNF alpha was analyzed by ELISA assay, before and after 16 weeks of intervention.
C Reactive Protein16 weeksC Reactive Protein was analyzed by ELISA assay, before and after 16 weeks of intervention.
Angiotensin II16 weeksAngiotensin II was analyzed by ELISA assay, before and after 16 weeks of intervention.
Angiotensin Converting Enzyme16 weeksAngiotensin Converting Enzyme was analyzed by ELISA assay, before and after 16 weeks of intervention.
Angiotensin 1-716 weeksAngiotensin 1-7 was analyzed by ELISA assay, before and after 16 weeks of intervention.
Adiponectin16 weeksAdiponectin was analyzed by ELISA assay, before and after 16 weeks of intervention.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026