Condition 1: The bio markers of cardiac injury response to two type resistance exercise, concentric failure set and configuration cluster sets. Condition 2: The response of left ventricles mechanical mechanism of athletic myocardium to two type resistance exercise, concentric failure set and configuration cluster sets. Condition 3: The response of right ventricles mechanical mechanism of athletic myocardium to two type resistance exercise, concentric failure set and configuration cluster sets. C
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Everyone with a history of weight training in advanced level People who have regular weight training during the weekly exercise program. People with absence of any disease Not taking any kind of exercise supplement
Exclusion criteria
Exclusion criteria: Training history less than 3 years No regular weight training in the past 18 months Absence of clinical symptoms associated with cardiovascular disease Not taking ergogenic supplements for at least 8 weeks before the test Absence of musculoskeletal disorders and diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Heart Ventricles dysfunction. Timepoint: Before and during the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: Philips EPIQ7 Echocardiography, hscTnI and Nt-proBNP with PATHFAST system, REAGENT KITS FOR CRITICAL CARE DIAGNOSTICS (LSI Medience Corporation 13-4, Uchikanda 1-chome, Chiyoda-ku Tokyo 101-8517 JAPAN). | — |
Secondary
| Measure | Time frame |
|---|---|
| Rate of Perceived Exertion (RPE). Timepoint: Before and during the intervention, after 30 min. Method of measurement: Borg's 6–20 RPE (Rating of Perceived Exertion) scale.;Hand grip strength. Timepoint: Before and during the intervention, after 30 min. Method of measurement: Yagami YG-200, Tokyo, Japan.;Heart rate. Timepoint: Before and during the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: Heart Rate monitor Polar v800, ECG connection to Philips EPIQ7 Echocardiography,.;Systolic blood pressure. Timepoint: Before the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: Finometer PRO (Finapress Medical Systems BV, Amsterdam, the Netherlands).;Diastolic blood pressure. Timepoint: Before the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: Finometer PRO (Finapress Medical Systems BV, Amsterdam, the Netherlands).;Systemic vascular resistance. Timepoint: Before the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: Finometer PRO (Finapress Medical Systems BV, Amsterdam, the Netherlands).;Mean blood pressure. Timepoint: Before the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: Finometer PRO (Finapress Medical Systems BV, Amsterdam, the Netherlands).;Haematocrit. Timepoint: Before and during the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: ELISA test.;Albumin. Timepoint: Before and during the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: ELISA test.;Cortisol. Timepoint: Before and during the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: ELISA test.;C-reactive protein. Timepoint: Before and during the intervention, after 30 min, 4, 6, 12 and 24 hours after intervention. Method of measurement: ELISA test.;Serum electr | — |
Countries
Iran (Islamic Republic of)
Contacts
University of Tehran Faculty of Physical Education and Sport Sciences