Difference in Acute Responses of Vascular Function to Moderate-intensity and High-intensity Interval Training in Healthy and Prehypertensive Individuals

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorUniversity of Ljubljana

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

18 - 50 years of age, BMI < 30, blood pressure (BP) within the optimal range according to the latest ESH guidelines (< 120 mmHg systolic and/or < 80 mmHg diastolic BP)

Sedentary or low active according to the Global Physical Activity Questionnaire (GPAQ) (Armstrong & Bull, 2006; Lim et al., 2012)

No prescribed medication and absence of chronic diseases

18 - 50 years of age, BMI < 30

Disqualifiers

Blood pressure out of the optimal range (normotensives)

High level of phyisical activity (moderate or high active according to GPAQ)

Hypotension

Chronic diseases

Trial design

Design model

Crossover

Treatments tested in this trial

  • Control-no treatment

    Other intervention

    30 minutes of rest

  • Exercise

    Other intervention

    30 minutes of Moderate-Intensity Continuous Exercise

  • Exercise

    Other intervention

    30 minutes of High-Intensity Interval Exercise

Treatment groups

45 Participants
are divided into 2 treatment groups
Group A: NormotensivePlacebo comparator 2 interventions
Group B: PrehypertensiveActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Arterial stiffness

Arterial stiffness will be measured by pulse wave velocity

Time frame
At the beginning of each visit (T0) and immediately after each acute stimulus (T1)
2

Microvascular function

Microvascular function will be mesured using near-infrared spectroscopy during and after a 5-minute occlusion of the brachial artery.

Time frame
At the beginning of each visit (T0) and immediately after each acute stimulus (T1)
3

Flow-mediated slowing

Flow-mediated slowing will be measured by pulse wave velocity deceleration after occlusion of the brachial artery.

Time frame
At the beginning of each visit (T0) and immediately after each acute stimulus (T1)

Secondary outcomes

1

Aerobic capacity

Aerobic capacity will be assessed using cardiopulmonary exercise test on a cycle ergometer.

Time frame
Baseline
2

Blood pressure

Systolic and Diastolic blood pressure will be measured using M6 Omron Device.

Time frame
Baseline
3

Blood markers

Blood samples will be taken from the median cubital vein and will include basic blood panel markers (HDL-C, LDL-C, TC, TG, glucose...)

Time frame
At the beginning of each visit (T0) and immediately after each acute stimulus (T1)

Other outcomes

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