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Effect of moderate and high resistant training on the inflammatory markers and cardiovascular risk factors in non-athlete students

Effect of moderate and high resistant training on the inflammatory markers and cardiovascular risk factors in non-athlete students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138809042770N1
Enrollment
30
Registered
2010-10-12
Start date
2008-01-30
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

cardiovascular risk factor and inflammatory markers. Atherosclerosis

Interventions

Intervention 1: Subjects in high intensitiy resistance group undergwent exercise regime consist of three sessions of resistance training per week for six consecutive weeks. In each session they did th
Subjects in high intensitiy resistance group undergwent exercise regime consist of three sessions of resistance training per week for six consecutive weeks. In each session they did three sets of 4-6
Subjects in moderate intensitiy resistance group undergwent exercise regime consist of three sessions of resistance training per week for six consecutive weeks. In each session they did three sets of
Subjects of the control group did not do any regular physical activities during the period of study.

Sponsors

Kurdistan University of Medical Sciences, vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 26 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Healthy young students with no previous record of any specific drug use and routine regular exercises during the last two years. Exclusion: Unhealthy, Doing regular exercise during the last two years.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Triglyceride, High-density lipoprotein, Low-density lipoprotein,Total cholesterol ,ApoA, ApoB. Timepoint: 6 weeks. Method of measurement: by collecting venous blood and measuring serum levels of related variables before and at the end of the study.;Lipoprotein Lipase. Timepoint: 6 weeks. Method of measurement: by collecting venous blood before and at the end of study and measuring serum levels using LPL kit.;Interleukin1 and Interleukin 6. Timepoint: 6 weeks. Method of measurement: by collecting venous blood before and at the end of study and measuring serum levels of related factors using Enzyme-linked immunosorbent assay (ELISA).;Hs-CRP (high-sensitivity CRP) and fibrinogen. Timepoint: 6 weeks. Method of measurement: by collecting venous blood before and at the end of study and measuring serum levels using related kits.;Body Mass Index. Timepoint: 6 weeks. Method of measurement: bybody composition analyzer (Biospase CO, Ltd).;Waist Hip Ratio. Timepoint: 6 weeks. Method of measurement: By measuring Hip and Waist circumferences by measuring tape.;Systolic and diastolic Blood pressure. Timepoint: 6 weeks. Method of measurement: sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSlahadin Ahmadi

Kurdistan University of Medical Sciences

slahadin@yahoo.com; slahadin@gmail.com; slahadin@muk.ac.ir+98 87 1662 1399

Outcome results

None listed

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