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Comparison of the effectiveness of 12 weeks of interval resistance training combined with Algomed supplementation on the control of proprotein subtilisin/caxin-converting enzyme type 9 and improvement of liver-expressed antimicrobial peptide 2 in obese men

Comparison of the effectiveness of 12 weeks of interval resistance training combined with Algomed supplementation on the control of proprotein subtilisin/caxin-converting enzyme type 9 and improvement of liver-expressed antimicrobial peptide 2 in obese men

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260417069089N1
Enrollment
44
Registered
2026-05-25
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Obesity. Overweight and obesity

Interventions

Intervention 1: Intervention group: Exercise training (interval resistance training protocol included 8 upper and lower body movements (squats, chest press, knee bends, biceps curls, leg press, barbel

Sponsors

University of Kurdistan
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
23 Years to 32 Years

Inclusion criteria

Inclusion criteria: Bmi>30 Obesity Waist–hip ratio (In obese men with a BMI over 30, there is no specific number for waist-to-hip ratio (WHR), as this ratio can vary from 0.85 to over 1.10 between individuals. But what is clinically important is the risk threshold: high metabolic risk (abdominal obesity): WHR > 0.90 and very high risk: WHR > 1.0)

Exclusion criteria

Exclusion criteria: Obesity men Non received drugs

Design outcomes

Primary

MeasureTime frame
PCSK9. Timepoint: Before the start of the intervention and 60 days after the start of the intervention. Method of measurement: Zelbio kite.;Leap2. Timepoint: Before the start of the intervention and 60 days after the start of the intervention. Method of measurement: Zelbio kite.—

Secondary

MeasureTime frame
BMI. Timepoint: Before the start of the intervention and 60 days after the start of the intervention. Method of measurement: Digital scale with a sensitivity of 0.1 g, high: Meter with an accuracy of one tenth of a centimeter.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaber

University of Kurdistan

saedsaber384@gmail.com0098 87 3562531

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026