Effect of Long-term Exercise on Haemostasis and Inflammation in Patients With Coronary Artery Disease
Primary Purpose
Coronary Artery Disease, Exercise, Inflammation
Status
Completed
Phase
Not Applicable
Locations
Faroe Islands
Study Type
Interventional
Intervention
Long-term exercise
Sponsored by
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring Cardiovascular Diseases, Exercise, Hemostasis, Inflammation
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years
- Angiographically verified coronary artery disease with stenosis of at least 50% or previous percutaneous coronary intervention (PCI)/coronary artery bypass graft (CABG) surgery.
- Diagnosis or revascularisation have been made at least 12 months prior to inclusion.
Exclusion Criteria:
- Inability to perform strenuous exercise
- Anticoagulant treatment
- Heart failure (ejection fraction <30% or NYHA >2)
- Implanted implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy (CRT)
- Serious arrhythmia requiring hospitalisation within the last 6 months
- Severe valvular heart disease
- Chronic obstructive pulmonary disease GOLD IV
Sites / Locations
- National Hospital of the Faroe Islands
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Long-term exercise
Usual care
Arm Description
Supervised exercise training three times a week for three months.
Patients are not offered supervised exercise.
Outcomes
Primary Outcome Measures
Changes in fibrinolytic biomarkers: tissue plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAI-1).
Changes in fibrinolytic biomarkers in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare fibrinolytic biomarkers assessed at baseline and after three months of supervised exercise for every patient.
Changes in clot maximum absorbance using the clot lysis assay.
Changes in maximum absorbance in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare clot maximum absorbance assessed at baseline and after three months of supervised exercise for every patient.
Changes in clot lysis time using the clot lysis assay.
Changes in clot lysis time in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare clot lysis time assessed at baseline and after three months of supervised exercise for every patient.
Changes in area under the curve using the clot lysis assay.
Changes in area under the curve in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare area under the curve assessed at baseline and after three months of supervised exercise for every patient.
Secondary Outcome Measures
Changes in platelet aggregation using arachidonic acid (ASPI) as agonist.
Changes in platelet aggregation with ASPI as agonist in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in platelet aggregation using adenosine diphosphate (ADP) as agonist.
Changes in platelet aggregation with ADP as agonist in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in platelet aggregation using thrombin receptor activating peptide-6 (TRAP) as agonist.
Changes in platelet aggregation with TRAP as agonist in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in thrombin generation assessing lag-time until initial thrombin generation.
Changes in lag-time until initial thrombin generation in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in thrombin generation assessing maximum concentration of thrombin.
Changes in maximum concentration of thrombin in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in thrombin generation assessing time to peak.
Changes in time to peak in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in thrombin generation assessing endogenous thrombin potential.
Changes in endogenous thrombin potential in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Changes in coagulation biomarkers: APTT, INR, Factor VIII, vWF.
Changes in coagulation biomarkers in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare coagulation biomarkers assessed at baseline and after three months of supervised exercise for every patient.
Changes in inflammatory biomarkers: CRP, multiple interleukins, tumor necrosis factor alpha (TNF-α), interferon gamma (INF-γ) and more.
Changes in inflammatory biomarkers in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare inflammatory biomarkers assessed at baseline and after three months of supervised exercise for every patient.
Full Information
NCT ID
NCT04268992
First Posted
February 10, 2020
Last Updated
August 2, 2023
Sponsor
Aarhus University Hospital
Collaborators
National Hospital of the Faroe Islands
1. Study Identification
Unique Protocol Identification Number
NCT04268992
Brief Title
Effect of Long-term Exercise on Haemostasis and Inflammation in Patients With Coronary Artery Disease
Official Title
Effect of Long-term Exercise on Haemostasis and Inflammation Compared With Standard Care in Patients With Stable Coronary Artery Disease: a Randomised Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
July 3, 2020 (Actual)
Primary Completion Date
June 4, 2021 (Actual)
Study Completion Date
January 16, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aarhus University Hospital
Collaborators
National Hospital of the Faroe Islands
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Introduction: Regular exercise training improves prognosis in patients with coronary artery disease (CAD). This study investigates whether the beneficial effects of exercise can be partly explained by favourable changes in haemostasis and inflammation.
Methods: 150 CAD patients are randomised to a supervised long-term exercise program (3 months) or usual care. Blood samples are obtained at baseline, 1.5 months, and 3 months after randomisation.
Results: The investigators will evaluate platelet turnover and aggregation, coagulation, fibrinolysis, and inflammatory markers before and after short- and long-term exercise, and the two randomised groups will be compared.
Perspectives: The present study will increase our knowledge of the beneficial mechanisms underlying the effect of exercise in CAD patients, potentially paving the way for improved exercise recommendations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Exercise, Inflammation, Hemostasis
Keywords
Cardiovascular Diseases, Exercise, Hemostasis, Inflammation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized controlled trial
Masking
Participant
Allocation
Randomized
Enrollment
142 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Long-term exercise
Arm Type
Experimental
Arm Description
Supervised exercise training three times a week for three months.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Patients are not offered supervised exercise.
Intervention Type
Other
Intervention Name(s)
Long-term exercise
Intervention Description
All patients randomised to long-term exercise will perform exercise training at least three times a week for three months. The exercise is supervised and individualised.
Primary Outcome Measure Information:
Title
Changes in fibrinolytic biomarkers: tissue plasminogen activator (t-PA) and plasminogen activator inhibitor-1 (PAI-1).
Description
Changes in fibrinolytic biomarkers in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare fibrinolytic biomarkers assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in clot maximum absorbance using the clot lysis assay.
Description
Changes in maximum absorbance in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare clot maximum absorbance assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in clot lysis time using the clot lysis assay.
Description
Changes in clot lysis time in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare clot lysis time assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in area under the curve using the clot lysis assay.
Description
Changes in area under the curve in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare area under the curve assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Changes in platelet aggregation using arachidonic acid (ASPI) as agonist.
Description
Changes in platelet aggregation with ASPI as agonist in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in platelet aggregation using adenosine diphosphate (ADP) as agonist.
Description
Changes in platelet aggregation with ADP as agonist in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in platelet aggregation using thrombin receptor activating peptide-6 (TRAP) as agonist.
Description
Changes in platelet aggregation with TRAP as agonist in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in thrombin generation assessing lag-time until initial thrombin generation.
Description
Changes in lag-time until initial thrombin generation in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in thrombin generation assessing maximum concentration of thrombin.
Description
Changes in maximum concentration of thrombin in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in thrombin generation assessing time to peak.
Description
Changes in time to peak in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in thrombin generation assessing endogenous thrombin potential.
Description
Changes in endogenous thrombin potential in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare the results assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in coagulation biomarkers: APTT, INR, Factor VIII, vWF.
Description
Changes in coagulation biomarkers in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare coagulation biomarkers assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Title
Changes in inflammatory biomarkers: CRP, multiple interleukins, tumor necrosis factor alpha (TNF-α), interferon gamma (INF-γ) and more.
Description
Changes in inflammatory biomarkers in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group). Moreover, the investigators will compare inflammatory biomarkers assessed at baseline and after three months of supervised exercise for every patient.
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Changes in cardiorespiratory performance: maximal oxygen uptake
Description
Changes in maximal oxygen uptake in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group).
Time Frame
3 months
Title
Changes in cardiorespiratory performance: maximal power output
Description
Changes in maximal power output in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group).
Time Frame
3 months
Title
Changes in physical health and mental health (quality of life) assessed by the SF-36v2 questionnaire.
Description
Changes in physical and mental health in coronary artery disease patients who are randomised to long-term exercise compared with patients randomised to usual care (control group).
Time Frame
3 months
Title
Incidence of adverse events associated with the exercise intervention.
Description
Number of adverse events (severe, moderate or mild) and training related injuries in coronary artery disease patients who are randomised to long-term exercise.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years
Angiographically verified coronary artery disease with stenosis of at least 50% or previous percutaneous coronary intervention (PCI)/coronary artery bypass graft (CABG) surgery.
Diagnosis or revascularisation have been made at least 12 months prior to inclusion.
Exclusion Criteria:
Inability to perform strenuous exercise
Anticoagulant treatment
Heart failure (ejection fraction <30% or NYHA >2)
Implanted implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy (CRT)
Serious arrhythmia requiring hospitalisation within the last 6 months
Severe valvular heart disease
Chronic obstructive pulmonary disease GOLD IV
Facility Information:
Facility Name
National Hospital of the Faroe Islands
City
Tórshavn
ZIP/Postal Code
100
Country
Faroe Islands
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
36241898
Citation
Kristiansen J, Sjuretharson T, Grove EL, Rasmussen J, Kristensen SD, Hvas AM, Mohr M. Feasibility and impact of whole-body high-intensity interval training in patients with stable coronary artery disease: a randomised controlled trial. Sci Rep. 2022 Oct 14;12(1):17295. doi: 10.1038/s41598-022-21655-w.
Results Reference
derived
Learn more about this trial
Effect of Long-term Exercise on Haemostasis and Inflammation in Patients With Coronary Artery Disease
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