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Clinical Trials/NCT02458456
NCT02458456
Completed
Not Applicable

Isometric Handgrip Exercise for Blood Pressure Management. A Randomized, Controlled Trial

University of New England, Australia1 site in 1 country120 target enrollmentAugust 2014
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
University of New England, Australia
Enrollment
120
Locations
1
Primary Endpoint
Change in systolic and diastolic blood pressure
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this project is to conduct a randomised controlled trial to assess the effect of performing isometric exercise using a handgrip dynamometer on blood pressure.

Detailed Description

Recent meta-analyses suggest isometric resistance training (IRT) may be superior to aerobic exercise for lowering blood pressure. A randomised controlled study will be conducted with participants who are either pre-hypertensive, blood pressure between 120/80 and 140/90, or on medication to control their blood pressure. Previous studies have utilised a sedentary control so we intend to use a sham group to determine if it can be used as a working control for future studies.

Registry
clinicaltrials.gov
Start Date
August 2014
End Date
December 2016
Last Updated
5 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
University of New England, Australia
Responsible Party
Principal Investigator
Principal Investigator

Deb Carlson

Sponsor-Investigator

University of New England

Eligibility Criteria

Inclusion Criteria

  • Those within the required age limits, both normotensive, pre-hypertensive, and those medicated for blood pressure management.

Exclusion Criteria

  • Younger than 30 years and older than 70 years; those deemed not to have the capacity to voluntarily participate, unable to participate under their doctor's recommendation, or with arthritis or carpal tunnel syndrome who may aggravate their condition with handgrip exercise.

Outcomes

Primary Outcomes

Change in systolic and diastolic blood pressure

Time Frame: Baseline and 8 weeks

Secondary Outcomes

  • Compare and contrast blood pressure changes between the 30% maximum voluntary contraction (MVC) hypertensive and 30% MVC normotensive groups(Baseline and 8 weeks)
  • Compare and contrast changes in blood pressure between the 5% maximum voluntary contraction (MVC) and 30% MVC hypertensive groups(Baseline and 8 weeks)

Study Sites (1)

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