Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
NCT07448818

Dynamic and Isometric Strength Training in Older Adults With Hypertension

Led by Raphael Mendes Ritti Dias · Updated on 2026-05-01

60

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This feasibility study aims to evaluate the effects of dynamic strength training and isometric strength training on cardiovascular health indicators, mental health, and neuromuscular fitness in older adults with hypertension. Participants will be randomly assigned to one of the two training modalities and will complete supervised exercise sessions throughout the intervention period. The study will provide preliminary evidence regarding the safety, acceptability, and potential impact of each training modality on health outcomes in this population.

CONDITIONS

Official Title

Dynamic and Isometric Strength Training in Older Adults With Hypertension

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of arterial hypertension and currently taking antihypertensive medication
  • Age 60 years or older
  • Resting blood pressure below 160/95 mmHg
  • No high cardiovascular risk according to American College of Sports Medicine criteria (for diabetes, fasting glucose <100 mg/dL and postprandial glucose <140 mg/dL)
  • Not participating in a structured exercise program for more than three months
  • No cognitive or functional limitations preventing participation in the exercise program
Not Eligible

You will not qualify if you...

  • Acute illnesses such as influenza, sinusitis, gastroenteritis, urinary tract infection, fever, inflammatory processes, or any clinical condition requiring rest or compromising safety during assessments or training
  • Decompensated clinical conditions including blood pressure spikes, chest pain, uncontrolled arrhythmias, shortness of breath at rest, asthma exacerbations
  • Decompensated diabetes mellitus with fasting glucose >180 mg/dL or postprandial glucose >250 mg/dL
  • Irregular use of medication
  • Any unstable clinical condition or additional risk for physical exercise

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Uninove

São Paulo, São Paulo, Brazil, 01525-000

Actively Recruiting

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Research Team

A

Adão Luis Monte L Monte, Ms

CONTACT

R

Raphael M Ritti-Dias, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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