Ireland
--:--IST
Active, not recruiting Not applicable

Aerobic Exercise and Resistant Hypertension

NCT05563077 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2022-10-05
Last updated
2025-09-18

Condition(s) studied

Resistant Hypertension

Investigational drug(s) / intervention(s)

Moderate-intensity interval training (MIIT)Moderate-intensity continuous training (MICT)

Moderate-intensity interval training (MIIT): MIIT group: participants will perform 3 sessions per week for 4 months. Each session will involve a ∼3 min warm-up (joint mobility exercises and walking at ∼2.2 METs), a ∼40-50 min main period (∼6-7 reps of 4 min at ∼4.2 METs, with 3 min of active recovery at ∼2.2 METs between each interval), and a ∼3-min cool-down (joint mobility exercises and walking at ∼2.2 METs). We will select the same aerobic dose of training (i.e., kcal/kg of body weight per week) to match total energy expenditure in both exercise groups.

Moderate-intensity continuous training (MICT): MICT group: participants will perform 3 sessions per week for 4 months. Each session will involve a ∼3 min warm-up (joint mobility exercises and walking at ∼2.2 METs), a ∼40-50 min main period at ∼3.2 METs, and a ∼3-min cool-down (joint mobility exercises and walking at ∼2.2 METs).

Study summary

This study will examine the effects of 4 months of aerobic interval training versus continuous aerobic training on ambulatory blood pressure (ABP) and novel plasma protein biomarkers in patients with resistant hypertension. A randomized controlled trial will be performed including two exercise groups and a control group: a) moderate-intensity interval training (MIIT); b) moderate-intensity continuous training (MICT); c) usual care. MIIT could represent a superior training modality that exceeds the benefits of MICT in patients with resistant hypertension.

Eligibility

Sex
ALL
Min age
30 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with resistant hypertension (RH) (i.e., systolic BP/diastolic BP \>130/80 mmHg according to the American College of Cardiology/American Heart Association) despite the concurrent use of three or more antihypertensive drugs - commonly including a diuretic, a long-acting calcium channel blocker, and a blocker of the renin-angiotensin system. RH also includes patients whose BP achieves target values on ≥ 4 antihypertensive. medications (i.e., 'controlled' RH). * Adherence to prescribed medications. * Willing to be randomized to one of the 3 groups. * Informed consent. Exclusion Criteria: * Exclusion criteria will include exercising more than 30 minutes on 3 days or more weekly. * Severe ischemic heart disease, major psychiatric disorder and other health contraindications that may interfere in the evaluations or interventions.

Primary outcome measure(s)

  • Change in 24-hour ambulatory blood pressure — Baseline to immediate post-treatment (4 months)
    Ambulatory SBP and DBP will be recorded with a validated oscillometric device over 24 hours.

Trial sites (1)

FacilityCityRegionStatus
Universidad Europea Madrid (UEM) Madrid Madrid
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05563077 on ClinicalTrials.gov ↗ ← All trials in Spain