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Study identifier: NCT07048509 Synced from ClinicalTrials.gov · July 28, 2026
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Difference in Acute Responses of Vascular Function to Moderate-intensity and High-intensity Interval Training in Healthy and Prehypertensive Individuals

Condition: Prehypertension (Elevated Blood Pressure) or Hypertension · Healthy  ·  Sponsor: University of Ljubljana

PhaseNA
Planned participants45
Who can joinAll sexes, 18 Years to 50 Years
Healthy volunteersYes

About this study

In this study, the investigators will evaluate acute changes in vascular function measures after moderate-intensity continuous and high-intensity interval exercise in healthy and prehypertensive individuals. Participants will be subjected to three separate visits: control condition (30 min rest), moderate-intensity continuous exercise, and high-intensity interval exercise. The investigators will measure aerobic capacity using a cardiopulmonary exercise test (CPET) using indirect gas-exchange to derive subsequent exercise intensity and maximal oxygen uptake. The investigators will evaluate different measures of vascular function (Pulse-wave velocity, Flow-mediated slowing, microvascular function) before and after each condition. The study will involve two groups of participants: healthy individuals and prehypertensive individuals. The investigators aim to establish the reliability and validity of less-established methods of vascular function assessment (flow-mediated slowing and microvascular function) against established measures (pulse-wave velocity). The acute response of vascular function to different exercise intensities has not yet been thoroughly researched using the aforementioned measures in individuals with similar characteristics to the proposed study cohort.

This description comes directly from the study's public registry record.

Talk to the study team

Armin H Paravlic, PhD  ·  +386015207840  ·  armin.paravlic@fsp.uni-lj.si

Always discuss trial participation with your own doctor first.

Locations (1)

University of Ljubljana, Faculty of sportLjubljana, SloveniaRecruiting

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Source record: clinicaltrials.gov/study/NCT07048509