Skip to main content
Clinical Trials/NCT07412600
NCT07412600
Completed
Not Applicable

High- and Low-Load Resistance Training to Failure Result in Similar Muscular Adaptations in Untrained Young Males

Akdeniz University1 site in 1 country22 target enrollmentStarted: December 18, 2021Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
22
Locations
1
Primary Endpoint
Maximal Dynamic Strength - Estimated One-Repetition Maximum (1RM) Using Submaximal Prediction and Epley Equation

Overview

Brief Summary

The goal of this clinical trial is to learn whether low-load resistance training performed to muscle failure can produce similar increases in muscle size and strength as high-load resistance training in healthy untrained young adult males.

The main questions it aims to answer are:

Does low-load resistance training (30% of one-repetition maximum) performed to failure increase muscle strength and muscle size to a similar extent as high-load resistance training (75% of one-repetition maximum)?

Are there differences in total training volume between low-load and high-load resistance training programs performed to failure?

Researchers will compare a low-load resistance training group to a high-load resistance training group to determine whether the magnitude of changes in muscle strength and hypertrophy differs between the two approaches.

Participants will:

Be randomly assigned to either a low-load (30% 1RM) or high-load (75% 1RM) resistance training group

Perform supervised leg extension exercises to the point of voluntary muscle fatigue three times per week for 6 weeks

Complete muscle strength testing (one-repetition maximum) before and after the training period

Undergo ultrasound measurements to assess muscle thickness and cross-sectional area of thigh muscles before and after the intervention

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 28 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age between 18 and 28 years
  • Healthy status as determined by self-report health screening
  • No participation in structured resistance training or lower-limb power training within the previous 12 months
  • Engaging only in recreational physical activity (no systematic lower-body resistance training)
  • Willingness to maintain usual daily routines throughout the study period
  • Agreement to refrain from any structured lower-body resistance training during the 6-week intervention
  • Provision of written informed consent

Exclusion Criteria

  • Any current or recent musculoskeletal injury affecting lower-limb function
  • History or presence of cardiovascular disease
  • History or presence of metabolic disorders
  • Resting hypertension (≥140/90 mmHg)
  • Regular tobacco use
  • Use of medications known to affect neuromuscular performance
  • Inability or unwillingness to comply with the training protocol

Arms & Interventions

LLRT

Experimental

Intervention: Low-load resistance training (30% 1RM) (Other)

HLRT

Experimental

Intervention: High-load resistance training (75% 1RM) (Other)

Outcomes

Primary Outcomes

Maximal Dynamic Strength - Estimated One-Repetition Maximum (1RM) Using Submaximal Prediction and Epley Equation

Time Frame: Baseline (Week 0) and immediately after completion of the 6-week intervention (Week 6)

Maximal strength will be estimated using a submaximal 1RM prediction protocol (8-10 repetitions) following a standardized warm-up. The highest load completed within the target repetition range will be used to calculate 1RM using the Epley equation (1RM = Load × \[1 + 0.033 × repetitions\]). Results will be expressed in kilograms (kg), with higher values indicating greater strength. Assessed at baseline and Week 4.

Muscle Thickness (MT) and Cross-Sectional Area (CSA) - Assessed by B-Mode Ultrasonography (LOGIQ S8, GE Healthcare)

Time Frame: Baseline (Week 0) and immediately after completion of the 6-week intervention (Week 6)

Muscle thickness (cm) and cross-sectional area (cm²) of the rectus femoris and vastus intermedius will be assessed using B-mode ultrasonography (LOGIQ S8, GE Healthcare, 2-8 MHz linear probe). Three images per site will be averaged for analysis. Higher values indicate greater muscle hypertrophy. Measurements performed at baseline and post-intervention by a blinded assessor.

Secondary Outcomes

  • Muscular Endurance - Repetitions to Volitional Failure at 50% of Estimated 1RM(Baseline (Week 0) and immediately after completion of the 6-week intervention (Week 6))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Abdullah Kayhan

Research Assistant

Akdeniz University

Study Sites (1)

Loading locations...

Similar Trials