Actively Recruiting

Phase Not Applicable
Age: 40Years - 75Years
All Genders
NCT06515795

Evaluation of Two Isometric Exercises in the Reduction of the Blood Pressure in People With Resistant Hypertension

Led by Universidade do Porto · Updated on 2024-07-23

15

Participants Needed

1

Research Sites

7 weeks

Total Duration

On this page

Sponsors

U

Universidade do Porto

Lead Sponsor

A

Aveiro University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Hypertension remains the main preventable cause of cardiovascular disease (CVD) and all-cause mortality, both in Europe and globally. Resistant hypertension, a severe phenotype of hypertension, is defined as a blood pressure (BP) that remains above the management goal despite using three different antihypertensive agents of different classes at the maximum or maximum tolerated dose, or controlled BP on four or more antihypertensive medications. Hypertension remains a poorly controlled risk factor on a global scale and the prevalence of resistant hypertension is also growing - it is now estimated to be around 10-20%. At the moment, there is robust evidence establishing the antihypertensive effects of exercise. The acute reduction of BP after a single bout of exercise is known as post-exercise hypotension. In recent years, the number of investigations into the benefits of isometric exercise in the treatment of hypertension has increased, due to its ease of access and potential for use. In a recently published meta-analysis, the authors pointed to isometric exercise as the most effective type of exercise in reducing systolic and diastolic BP. Given the scarceness of data regarding the safety and efficacy of isometric exercise in individuals with resistant hypertension and since the acute response to exercise may help to identify people who respond to exercise as antihypertensive therapy, the objective of this study is to analyse the acute effect on BP levels of two different isometric exercises - isometric handgrip (IHG) and isometric wall squat (IWS), regarding safety and efficacy, in people with resistant hypertension. The aim is to analyse if isometric exercises are safe in this population, through the assessment of BP during the execution of the exercises. Besides that, the comparison of IHG and IWS with the control session and between one and another, will help to understand which form of isometric exercise is most effective and has the longest lasting impact on reducing BP. Each participant must complete an acclimatization session, in which the procedures will be explained, data will be collected and the intensity of IHG and IWS will be assessed. Subsequently, each participant must complete three randomly assigned experimental sessions: a non-exercise control session and two exercise sessions, in which they will follow the protocols currently used in the literature (IHG at 30% of Maximum Voluntary Contraction and IWS at 95% of peak Heart Rate).

CONDITIONS

Official Title

Evaluation of Two Isometric Exercises in the Reduction of the Blood Pressure in People With Resistant Hypertension

Who Can Participate

Age: 40Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 40 to 75 years old
  • Diagnosed with resistant hypertension
  • On stable blood pressure medication for at least 6 months
Not Eligible

You will not qualify if you...

  • Secondary hypertension
  • Heart failure
  • Peripheral artery disease
  • Atrial fibrillation
  • Chronic obstructive pulmonary disease
  • Renal failure
  • Stroke or cardiovascular event in the previous 3 months
  • Changes in blood pressure medication in the previous 6 months
  • Regular exercise participation (2 or more times per week) in the previous 3 months
  • Any contraindication to exercise
  • Neurological or orthopedic conditions affecting exercise participation, such as Parkinson's disease or knee osteoarthritis
  • Low score (<6) on the MMAS-8 medication adherence scale

AI-Screening

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Trial Site Locations

Total: 1 location

1

Local Health Unit of the Aveiro Region

Aveiro, Portugal

Actively Recruiting

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Research Team

J

José Lopes, Master

CONTACT

J

José Oliveira, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

3

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