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Stable Versus Unstable Resistance Training Effects on Physical Fitness and Physiological Biomarkers of Untrained Male University Students

A

Addis Ababa University

Status

Active, not recruiting

Conditions

Health Young Males
No Condition

Treatments

Other: resistance training

Study type

Interventional

Funder types

Other

Identifiers

NCT07349342
CNS-IRB/05/2015/2023

Details and patient eligibility

About

The goal of this clinical trial is to learn the effects of stable and unstable resistance training on physical fitness, kidney function and blood lipid tests in healthy young male volunteers. The main questions it aims to answer are:

  • Do both stable and unstable resistance training increase the level of urinary protein clearance greater than the control group?
  • What is the difference in improvement of lipid profiles among the groups?
  • Does unstable resistance training mode rise muscular endurance greater than stable resistance training?

Researchers will compare stable and unstable resistance training to see if there are differences on physical fitness measures, blood lipid and urinary protein tests.

Participants, in their respective group will receive ten weeks of:

  • Stable resistance training
  • Unstable resistance training or
  • No exercise training intervention

Full description

This study included volunteer male untrained students living at Kotebe University of Education. Priori statistical power analysis (G*Power version 3.1.9.2, Stuttgart, Germany) was used to estimate the sample size. Based on earlier research, a moderate to high effect size (0.295) was assumed, and considering a dropout probability of 10%, a sample of 54 participants was enough to meet adequate statistical power. All participants provided written informed consent to participate in this study. The training protocol will include ten resistance exercises for each intervention, performed three times a week for 10 weeks. Each session lasts 60 minutes, including a 10 to 15-minute warm-up, a 40-minute main exercise targeting core, upper, and lower limb muscles, and a 5 to 10-minute cool-down and stretching. The protocol will adhere to basic training principles like overload, progression, and specificity. The training will take place in the university gymnasium. The study will be conducted in accordance with local legislation and institutional requirements. It will be strictly governed by the ethical principles of the Declaration of Helsinki.

Enrollment

54 patients

Sex

Male

Ages

20 to 24 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • No resistance training within the previous six months
  • Completing a written informed consent document
  • Responding to the physical activity readiness questionnaire (PAR-Q) and becoming convenient

Exclusion criteria

  • A history of musculoskeletal injury
  • Chronic diseases, including known kidney disease
  • A habit of alcohol or drug abuse

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

54 participants in 3 patient groups

Unstable resistance training group
Experimental group
Description:
Receiving total body resistance exercise (TRX) training intervention
Treatment:
Other: resistance training
Other: resistance training
Control group
No Intervention group
Description:
no any structured exercise training intervention
stable resistance training group
Experimental group
Description:
receiving traditional resistance training intervention
Treatment:
Other: resistance training
Other: resistance training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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