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.
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
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:
- The identification of the new markers of cardiovascular risk in patients with arterial hypertension..
- The identification of the new markers of progression from normal left ventricular diastolic function to left ventricular diastolic dysfunction.
- The identification of the new noninvasive markers of progression to symptomatic heart failure.
- 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.
- Multivariate assessment of cardiovascular response to the controlled exercise, taking into account left ventricular diastolic function and symptoms of heart failure.
- 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 group | Role | What they receive |
|---|---|---|
| Group N | The subjects with no symptoms of HF and normal left ventricular diastolic function (no less than 40 subjects) | |
| Group D | The subjects with no symptoms of HF and left ventricular diastolic dysfunction (no less than 40 subjects) | |
| Group D_HF | The 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.
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)
death from any cause
Measured: 48 months
death from cardiovascular causes
Measured: 48 months
myocardial infarction
Measured: 48 months
decompensated heart failure
Measured: 48 months
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.
- First posted18 Dec 2015 (estimated)
- Study startJan 2015
- Primary completionDec 2020
- Study completionDec 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for HypertensionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Military Institute od Medicine National Research Institute
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Paweł Krzesiński, Military Institute od Medicine National Research Institute
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
Study at a glance
From the registry record, last updated by the sponsor on 26 Feb 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Multivariate ASSEssment of CardiovascUlar Response to the Controlled Exercise in Patients With Hypertension - Prospective and Observational Study (ASSECURE Study)
- ClinicalTrials.gov ID
- NCT02634866
- Acronym / sponsor ID
- ASSECURE / 0000000336
- Conditions
- Hypertension
- Keywords
- hypertension, exercise, diastolic heart failure
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 114 participants (actual)
- Lead sponsor
- Military Institute od Medicine National Research InstituteUniversity, hospital or other
- Study start
- Jan 2015 (actual)
- Primary completion
- Dec 2020 (actual)
- Study completion
- Dec 2020 (actual)
- First posted
- 18 Dec 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
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:
- The identification of the new markers of cardiovascular risk in patients with arterial hypertension..
- The identification of the new markers of progression from normal left ventricular diastolic function to left ventricular diastolic dysfunction.
- The identification of the new noninvasive markers of progression to symptomatic heart failure.
- 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.
- Multivariate assessment of cardiovascular response to the controlled exercise, taking into account left ventricular diastolic function and symptoms of heart failure.
- 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)
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Group N | – | –The subjects with no symptoms of HF and normal left ventricular diastolic function (no less than 40 subjects) |
| Group D | – | –The subjects with no symptoms of HF and left ventricular diastolic dysfunction (no less than 40 subjects) |
| Group D_HF | – | –The subjects with symptoms of HF and left ventricular diastolic dysfunction (no less than 40 subjects) |
Who may qualify
- Ages
- 40 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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).
Key inclusion criteria (3 listed)
- patients of either sex
- age 40-75 years
- arterial hypertension diagnosed ≥3 months before recruitment.
Key exclusion criteria (11 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
complex end-point (death from cardiovascular causes and/or myocardial infarction and/or stroke and/or decompensated heart failure)
Time frame: 48 months
Any of the following cardiovascular events: death from cardiovascular causes and/or myocardial infarction and/or stroke and/or decompensated heart failure
5 secondary outcomes
death from any cause
Time frame: 48 months
death from cardiovascular causes
Time frame: 48 months
myocardial infarction
Time frame: 48 months
decompensated heart failure
Time frame: 48 months
stroke
Time frame: 48 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Feb 2021.
- Derived from this study: PubMed 40065085Skalska 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.
- Individual participant dataSharing planned: Undecided
Related trials for Hypertension
Not yet recruiting
PAUL® Glaucoma Implant Safety and Effectiveness Study
Refractory Glaucoma
RecruitingObservational study
Asthma and Primary Arterial Hypertension: an Inflammatory Link?
Asthma Bronchial
RecruitingObservational study
Clevidipine for the Antihypertensive Treatment of Acute Intracerebral Hemorrhage
Intracerebral Hemorrhage, Stroke
RecruitingPhase 1/2
HS235 Study in Overweight and Obese Participants With Combined Pre and Post-Capillary Pulmonary Hypertension Due to Heart Failure With Preserved Ejection Fraction
Pulmonary Hypertension, Heart Failure With Preserved Ejection Fraction
Recruiting
Dry Weight Reduction Intervention Via Extra Ultrafiltration
Fluid Accumulation, Blood Pressure Management
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.