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Effect of High-Intensity Interval Training on Cardiac Rehabilitation among Myocardial Infarction Patients

Comparison of the Effectiveness of Cardiac Rehabilitation based on High- volume (HV-HIIT) and low-volume (LV-HIIT) High-Intensity Interval Training on Serum levels of some miRNAs, myocardial contractile biomarkers , Inflammatory and Functional Markers in Myocardial Infarction Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201022049111N1
Enrollment
128
Registered
2020-11-29
Start date
2020-11-19
Completion date
Unknown
Last updated
2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial infarction. Chronic ischemic heart disease

Interventions

Intervention 1: Intervention group 1 (HV-HIIT group): A training session on the treadmill at 4 × 4-minute intervals at 90% of HRr with 3 minutes of active recovery at 65% of HRr between intervals and

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: MI type 1 and having an ejection fraction of 40% At least six to two years have passed since the diagnosis and angioplasty Be in a stable condition without drug changes In class II, I have cardiac function. Maximum metabolic equivalent to or more than 5 MET

Exclusion criteria

Exclusion criteria: Metabolic diseases such as diabetes and obesity Variable blood pressure Congestive heart failure Dangerous arrhythmias Liver and kidney failure Chronic obstructive pulmonary disease Neuromuscular disorders

Design outcomes

Primary

MeasureTime frame
Expression of miR-1. Timepoint: Before and after the intervention. Method of measurement: Real time – PCR.;C-Reactive Protein (CRP). Timepoint: Before and after the intervention. Method of measurement: by using the immunometric assay technique method and ELISA Kit.;Uric acid. Timepoint: Before and after the intervention. Method of measurement: by using the immunometric assay technique method and ELISA Kit.;Expression of miR-208. Timepoint: Before and after the intervention. Method of measurement: Real time – PCR.;Expression of miR-133. Timepoint: Before and after the intervention. Method of measurement: Real time – PCR.;Expression of mRNACapas3. Timepoint: Before and after the intervention. Method of measurement: Real time – PCR.;CK-mb. Timepoint: Before and after the intervention. Method of measurement: by using the immunometric assay technique method and ELISA Kit.;Troponin. Timepoint: Before and after the intervention. Method of measurement: by using the immunometric assay technique method and ELISA Kit.

Secondary

MeasureTime frame
Quality of Life. Timepoint: Before and after the intervention. Method of measurement: Quality of Life Questionnaire.;Ejection fraction. Timepoint: Before and after the intervention. Method of measurement: Echocardiography and Simpson.;Systolic blood pressure. Timepoint: Before and after the intervention. Method of measurement: Digital blood pressure device.;Maximal Oxygen Consumption (peak VO2). Timepoint: Before and after the intervention. Method of measurement: Exercise stress test.;End-systolic volume. Timepoint: Before and after the intervention. Method of measurement: M-mode echocardiography.;Diastolic blood pressure. Timepoint: Before and after the intervention. Method of measurement: Digital blood pressure device.;End-Diastolic volume. Timepoint: Before and after the intervention. Method of measurement: M-mode echocardiography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMustafa Cheraghi

Khoram-Abad University of Medical Sciences

Dcheraghi406@gmail.com+98 66 4230 8790

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026