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Completed

NCT Number: NCT02930330

Interval Training in Cardiac Rehabilitation

The purpose of this study is to determine whether high intensity interval training (INT) is more effective in suppressing platelet reactivity than continuous, moderate intensity training (CONT) in patients undergoing cardiac rehabilitation after percutaneous coronary intervention.

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Key information

Conditions

Atherosclerosis Arterial Occlusive Diseases Arteriosclerosis Behavior Cardiovascular Diseases Coronary Artery Disease Coronary Disease Heart Diseases Motor Activity Myocardial Ischemia Vascular Diseases

Age range

45 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

MUVienna

Vienna, 1090, Austria

About this study

Background: Platelets play an important role in cardiovascular disease: First, they promote the development of atherosclerotic lesions, and second, platelets form vessel occluding thrombi on top of (ruptured) lesions, ultimately leading to thrombotic events like myocardial infarctions (MCI). Whereas acute, strenuous exercise causes platelet activation and transiently increases the risk for MCIs, long-term chronic exercise training results in a clear reduction of both platelet activation and MCI incidence.

Exercise training plays a key role in cardiac rehabilitation, since improvements in cardiorespiratory fitness (CRF) are associated with decreased mortality in these patients. With respect to CRF improvements, high-intensity interval training has been demonstrated to be more effective than moderate-intensity continuous exercise. However, the beneficial effect of high-intensity interval training on platelet function in patients with cardiovascular disease has never been investigated.

Scientific question: The aim of this study is to determine the effect of interval training in cardiac rehabilitation on platelet function.

Hypotheses: Cardiac rehabilitation with interval training components (INT) reduces

  • platelet activation and platelet reactivity at physical rest
  • changes of platelet activation and -reactivity induced by acute, strenuous exercise to a greater extent than cardiac rehabilitation consisting exclusively of moderate-intensity continuous exercise training (CONT).

Work program: 80 patients at the beginning of phase II cardiac rehabilitation will be randomly assigned to an interval group or to a control group. In both groups, patients will exercise 4x / week for 12 weeks. At the beginning, after 6 weeks and at the end an exercise test will be carried out. Blood will be taken before (platelet function at rest) and immediately after each exercise test (platelet function after acute, strenuous exercise). Basal platelet activation as well as platelet responsiveness towards a platelet agonist (platelet reactivity) will be analyzed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • No regular exercise training within the last 6 months
  • Dual anti-platelet therapy (low-dose aspirin plus ADP(adenosine diphosphate)-receptor antagonist)
  • Status post percutaneous coronary intervention after recent acute coronary syndrome as underlying reason for current rehabilitation
  • Eligibility for outpatient cardiac rehabilitation according to Table I in Niebauer et al. 2013 (PMID: 22508693)

Exclusion criteria

  • Type II diabetes mellitus
  • Aortic aneurysm / dissection
  • Uncontrolled hypertension (>180/110 mmHg)
  • Pulmonary hypertension (>55 mmHg)
  • Previously known hereditary platelet disorders
  • Disorders of plasmatic coagulation
  • Anemia (Hb < 13g/dl)
  • History of end-stage liver or kidney disease

Treatment and study plan

INT

Behavioral
  • 5 min warm-up (40% Pmax*)
  • 30 min high intensity interval training (1 min 100% Pmax, 1 min 20% Pmax, in alternating sequence)
  • 10 min cool-down (30% Pmax)

Pmax*: Maximal power output (Watt) achieved at the end of an incremental exercise test.

Other names: High intensity interval training

CONT

Behavioral
  • 5 min warm-up (40% Pmax*)
  • 30 min moderate intensity continuous training (60% Pmax)
  • 10 min cool-down (30% Pmax)

Pmax*: Maximal power output (Watt) achieved at the end of an incremental exercise test.

Other names: Moderate intensity continuous training

Primary outcomes

  1. Platelet reactivity at physical rest: EC50 of TRAP-6 in terms of platelet CD62P expression. Unit of Measure: µM (Micromolar)

    Time frame: 6 weeks

    Platelet reactivity as measured by half maximal effective concentration (EC50) of the platelet agonist TRAP-6 (Thrombin receptor activating peptide-6; SFLLRN) in terms of platelet CD62P (P-selectin) expression, as described in Heber et al. 2016 (PMID: 26909532). The percentage of CD62P expressing platelets is quantified by flow cytometry without and with increasing concentrations of the platelet agonist TRAP-6. EC50 of TRAP-6 is estimated by fitting a four parameter logistic dose-response curve to flow cytometry data as a function of agonist concentration, aggregating multiple measurements to one reported value (EC50) with the unit µM.

    Treatment effects on platelet reactivity at physical rest after 6 weeks (INT vs. CONT) are estimated by ANCOVA, with baseline values as covariate.

Secondary outcomes

  1. Platelet reactivity at physical rest: EC50 of TRAP-6 in terms of platelet CD62P expression. Unit of Measure: µM

    Time frame: 12 weeks

    Platelet reactivity as measured by half maximal effective concentration (EC50) of the platelet agonist TRAP-6 (Thrombin receptor activating peptide-6; SFLLRN) in terms of platelet CD62P (P-selectin) expression. The percentage of CD62P expressing platelets is quantified by flow cytometry without and with increasing concentrations of the platelet agonist TRAP-6. EC50 of TRAP-6 is estimated by fitting a four parameter logistic dose-response curve to flow cytometry data as a function of agonist concentration, aggregating multiple measurements to one reported value (EC50) with the unit µM.

    Treatment effects on platelet reactivity at physical rest after 12 weeks (INT vs. CONT) are estimated by ANCOVA, with baseline values as covariate.

  2. Cardiorespiratory fitness: Maximal power output

    Time frame: 6 weeks

    Maximal power output (Watt / kg bodyweight) at the end of an incremental exercise test

  3. Cardiorespiratory fitness: Maximal power output

    Time frame: 12 weeks

    Maximal power output (Watt / kg bodyweight) at the end of an incremental exercise test

  4. Cardiorespiratory fitness: Maximal oxygen consumption

    Time frame: 6 weeks

    Maximal oxygen consumption (ml/min/kg bodyweight) at the end of an incremental exercise test

  5. Cardiorespiratory fitness: Maximal oxygen consumption

    Time frame: 12 weeks

    Maximal oxygen consumption (ml/min/kg bodyweight) at the end of an incremental exercise test

Sponsors and collaborators

Lead sponsor

Medical University of Vienna

Other

Collaborators

  • Austrian Heart Funds
  • Medical Scientific Fund of the Mayor of Vienna

Registry information

Official study title

Interval Training in Cardiac Rehabilitation: Effects on Cardiorespiratory Fitness and Platelet Function - A Randomized Controlled Trial

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Oct 12, 2016
Registry last updated
Aug 31, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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