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HypertensionASSECURENCT02634866

Cardiovascular Response to Exercise in Hypertension

An observational study of Hypertension, run by Military Institute od Medicine National Research Institute at 1 site in Poland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Arterial hypertension (AH) is an important clinical social and economic problem, related to the increased cardiovascular risk. AH is associated with cardiovascular hemodynamic alterations, including left ventricular diastolic dysfunction (LVddf). Read more about this study

Who is it for?
Ages 40 to 75 years
Conditions the study is for
Hypertension
How many people
114 participants
Where
1 sitePoland
Study dates
Jan 2015to Dec 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: No less than 120 hypertensive subjects (both sexes, aged 40-75 years) will be enrolled, including those with: 1/ no symptoms of HF and normal LV diastolic function (group N, no less than 40 subjects), 2/ no symptoms of HF and LVddf (group D, no less than 40 subjects), 3/ with symptoms of both HF and LVddf (group D_HF, no less than 40 subjects).

Who may be able to join

  • patients of either sex
  • age 40-75 years
  • arterial hypertension diagnosed ≥3 months before recruitment.

Who cannot join

  • office blood pressure > 160/100 mmHg
  • coronary artery disease
  • systolic heart failure (LVEF below 45%) and/or severe heart defect (i.e. valvular disease)
  • severe pulmonary diseases (COPD stage C/D, uncontrolled asthma, pulmonary hypertension, pulmonary embolism)
  • chronic kidney disease (MDRD eGFR<60 ml/min/1.73m2)
  • severe inflammatory disease
Show all 11Show fewer
  • severe mental and physical disorders
  • polyneuropathy
  • obesity with BMI > 40 kg/m2
  • life expectancy less than 12 months in the opinion of the physician
  • patients' refusal to participate.

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • Military Institute of Medicine

    Warsaw, Masovian Voivodeship, 04-141

Other trials in Poland

About this study

Official title: Multivariate ASSEssment of CardiovascUlar Response to the Controlled Exercise in Patients With Hypertension - Prospective and Observational Study (ASSECURE Study)

Arterial hypertension (AH) is an important clinical social and economic problem, related to the increased cardiovascular risk. AH is associated with cardiovascular hemodynamic alterations, including left ventricular diastolic dysfunction (LVddf). In consequence of increased blood pressure, the effectiveness of LV as a blood pump decreases and the symptoms of heart failure (HF) may occur. Thus, the identification of noninvasive markers related with the progression from the asymptomatic AH to LVddf/HFpEF would be beneficial.

Another issue is that the diagnostic difficulties in patients with LVddf and HFpEF stem from the limited possibility to assess the hemodynamic response to exercise. Thus, there is a need for more detailed methods of cardiovascular monitoring while exercise testing.

Read more

We hypothesize that some new noninvasive hemodynamic parameters, characterizing left ventricular (LV) function and arterial stiffness, may help to predict the risk of cardiovascular events and future occurrence of LVddf/HFpEF. Moreover, we assume that cardiopulmonary exercise test (CPET), completed with new methods of noninvasive hemodynamic monitoring (impedance cardiography and applanation tonometry), would provide additional value in the assessment of the cardiovascular hemodynamic response to exercise.

The study is intended to verify these hypothesis.

Read the detailed description

Arterial hypertension (AH) is an important clinical social and economic problem, related to the increased cardiovascular risk.

AH is associated with cardiovascular hemodynamic alterations, including left ventricular diastolic dysfunction (LVddf). In consequence of increased blood pressure, the effectiveness of LV as a blood pump decreases and the symptoms of heart failure (HF), even with preserved ejection fraction (HFpEF), may occur. At the early stage, patients' complaints are not specific and difficult to clinical interpretation. As a consequence, these subjects frequently remain undiagnosed. Thus, the identification of noninvasive markers related with the progression from the asymptomatic AH to LVddf/HFpEF would be beneficial.

Another issue is that the diagnostic difficulties in patients with LVddf and HFpEF stem from the limited possibility to assess the hemodynamic response to exercise. Thus, there is a need for more detailed methods of cardiovascular monitoring while exercise testing.

The investigators hypothesize that some new noninvasive hemodynamic parameters, characterizing left ventricular (LV) function and arterial stiffness, may help to predict the risk of cardiovascular events and future occurrence of LVddf/HFpEF. Moreover, the investigators assume that cardiopulmonary exercise test (CPET), completed with new methods of noninvasive hemodynamic monitoring (impedance cardiography and applanation tonometry), would provide additional value in the assessment of the cardiovascular hemodynamic response to exercise.

Aims:

  1. The identification of the new markers of cardiovascular risk in patients with arterial hypertension..
  2. The identification of the new markers of progression from normal left ventricular diastolic function to left ventricular diastolic dysfunction.
  3. The identification of the new noninvasive markers of progression to symptomatic heart failure.
  4. The evaluation of the feasibility and usefulness of new methods of noninvasive hemodynamic monitoring (impedance cardiography and applanation tonometry) in the assessment of the cardiovascular hemodynamic response to exercise.
  5. Multivariate assessment of cardiovascular response to the controlled exercise, taking into account left ventricular diastolic function and symptoms of heart failure.
  6. The relation between laboratory markers of left ventricular remodeling with resting and exercise (noninvasive) hemodynamics.

The study will be performed in a prospective and observational design. No less than 120 hypertensive subjects will be enrolled.

After recruitment the following assessment will be performed:

  • anamnesis and physical examination with anthropometrics (including body composition analysis with use of bioimpedance method);
  • electrocardiogram;
  • echocardiography (resting), including assessment of left ventricular systolic (2-D left ventricular ejection fraction, longitudinal strain) and diastolic function (including tissue Doppler imaging);
  • impedance cardiography (resting);
  • Applanation tonometry (resting);
  • 24-h Holter-ekg (including heart rate variability analysis);
  • 24-h ambulatory blood pressure monitoring;
  • flow-mediated dilation of brachial artery (FMD);
  • 6-minute walking test (6-MWT);
  • Cardiopulmonary exercise test (CPET), supported by hemodynamic monitoring with impedance cardiography and applanation tonometry;
  • Quality of life assessment (SF 36 questionnaire);
  • Laboratory tests (including creatinine, urea, uric acid, lipids, glucose, microalbuminuria, N-terminal of the prohormone brain natriuretic peptide, galectin-3, copeptin, soluble ST2, Growth differentiation factor 15 (GDF-15), human tissue inhibitor of metalloproteinases 1 (TIMP-1), metalloproteinase 2 (MMP-2), metalloproteinase 9 (MMP-9), syndecan-1).

After 12 months (first control visit) and 24 months (second control visit) the echocardiography and clinical assessment (HF symptoms) will be performed to identify: 1/ patients with new onset LVDdf (among group N); 2/ patients with new onset HF (among group D)

Morover, the follow-up of min 48 months concerning cardiovascular events will be performed (as defined below)

Conditions
Hypertension
Keywords
hypertension, exercise, diastolic heart failure
Medical subject headings
Hypertension, Motor Activity, Heart Failure, Diastolic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02634866
Study groupRoleWhat they receive
Group NThe subjects with no symptoms of HF and normal left ventricular diastolic function (no less than 40 subjects)
Group DThe subjects with no symptoms of HF and left ventricular diastolic dysfunction (no less than 40 subjects)
Group D_HFThe subjects with symptoms of HF and left ventricular diastolic dysfunction (no less than 40 subjects)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. complex end-point (death from cardiovascular causes and/or myocardial infarction and/or stroke and/or decompensated heart failure)

    Any of the following cardiovascular events: death from cardiovascular causes and/or myocardial infarction and/or stroke and/or decompensated heart failure

    Measured: 48 months

Secondary outcomes (5)
  1. death from any cause

    Measured: 48 months

  2. death from cardiovascular causes

    Measured: 48 months

  3. myocardial infarction

    Measured: 48 months

  4. decompensated heart failure

    Measured: 48 months

  5. stroke

    Measured: 48 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Dec 2015 (estimated)
  2. Study startJan 2015
  3. Primary completionDec 2020
  4. Study completionDec 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
114 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02634866
Sponsor's protocol ID
0000000336
Acronym
ASSECURE
Status last verified
Feb 2021
First submitted
16 Dec 2015
Last updated
26 Feb 2021
Results posted
No
Data monitoring committee
No
Individual data sharing
Undecided

Publications

  • Skalska P, Kurpaska M, Banak M, Krzesinski P. Hypertensive women with dyspnea exhibit an unfavorable central blood pressure response to exercise. Hypertens Res. 2025 May;48(5):1759-1767. doi: 10.1038/s41440-025-02171-6. Epub 2025 Mar 10.

    PubMed 40065085

Questions about this trial

What is this clinical trial studying?

An observational study of Hypertension, run by Military Institute od Medicine National Research Institute at 1 site in Poland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Feb 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

complex end-point (death from cardiovascular causes and/or myocardial infarction and/or stroke and/or decompensated heart failure) (time frame: 48 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02634866, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Feb 2021.

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Cardiovascular Response to Exercise in Hypertension | AzTrials