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The effect of high intensity resistance exercise on the biological and mechanical mechanism of the heart

The effect of two type resistance exercise, concentric failure set and configuration cluster sets on bio markers of myocardium injury and left and right ventricles mechanical mechanism in athletic

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190403043158N1
Enrollment
24
Registered
2020-09-27
Start date
2018-11-11
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

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

Interventions

Intervention 1: Intervention 1: concentric failure sets with circuit pattern consist of 9 movements: in front squat, bench press, dead lift, shoulder press, in front lunge, weight pull up, roman lift,

Sponsors

Vice chancellor for research, Faculty of Tehran University, Physical Education and Sport Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 27 Years

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

MeasureTime 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

MeasureTime 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

Public ContactRasoul Dokht Abdiyan

University of Tehran Faculty of Physical Education and Sport Sciences

rasoulabdiyan11@gmail.com+98 21 6697 5985

Outcome results

None listed

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