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Clinical Trials/NCT07379385
NCT07379385
Enrolling By Invitation
Not Applicable

The Effect of Weekly Set Volume of Resistance Training on Strength and Hypertrophy

Universidade Norte do Paraná1 site in 1 country57 target enrollmentStarted: January 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Enrolling By Invitation
Sponsor
Universidade Norte do Paraná
Enrollment
57
Locations
1
Primary Endpoint
Maximum dynamic strength (1RM)

Overview

Brief Summary

The progressive loss of strength and muscle mass is a natural aging process, with direct implications for functional capacity. Resistance training (RT) is considered the main intervention to counteract this decline. Although the RT guidelines are well established, the ideal weekly set volume to maximize strength and hypertrophy gains in older adults remains unknown. The purpose of this study is to investigate the effects of different volumes of weekly sets of RT on muscle strength and hypertrophy in older adults

Detailed Description

BACKGROUND: The progressive loss of strength and muscle mass is a natural process of aging, with direct implications for functional capacity. Resistance training (RT) is considered the main intervention to counteract this decline. Although RT guidelines are well established, the ideal weekly volume of sets to maximize strength and hypertrophy gains in older adults remains unknown. PURPOSE: To investigate the effects of different weekly RT volumes on lower limb muscle strength and hypertrophy (quadriceps femoris) in older adults. METHODS: Fifty-seven older adults of both sexes will be matched for maximum dynamic strength (one repetition maximum - 1RM) and randomly divided into 03 groups: [Low Volume (LV = 6 sets/week, n = 19), Moderate Volume (MV = 18 sets/week, n = 19) and High Volume (LV = 30 sets/week, n = 18)]. All participants will undergo a 10-week resistance training protocol (3x/week), consisting of 8 exercises: bench press, leg press, seated row, leg extension, bicep curl, leg curl, triceps pulley, and seated calf raise. Only the leg extension and leg press exercises will be performed with different volumes of sets (VB = 1 set/exercise; VM = 3 sets/exercise; VA = 5 sets/exercise). The number of repetitions per set will be 8-12, and the training load will be adjusted every two weeks based on the maximum number of repetitions performed in the last training session. The following dependent variables will be analyzed before and after the training program: (1) maximum dynamic strength (1RM) and (2) maximum voluntary isometric contraction (MVIC) in the leg extension exercise, (3) muscle hypertrophy (thickness) of the quadriceps muscle and rectus femorisusing ultrasound images, and (4) rating of perceived exertion (RPE) and (5) affective responses (pleasure and displeasure) after training sessions. Data will be tested for normality and homogeneity using the Shapiro-Wilk's and Levene's tests, respectively. Changes over time and between groups will be analyzed with two-way repeated measures ANOVA tests. Violation of sphericity was corrected using the Greenhouse-Geisser method. When significant differences will be confirmed with the ANOVA, multiple comparison testing will be performed using the Bonferroni post hoc correction to identify these differences. Values will be expressed as mean (standard deviation and 95% confidence interval). The significance level was set at p < 0.05.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
65 Years to 80 Years (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age between 65 and 80 years

Exclusion Criteria

  • not having used any medication or substance that affects or improves muscle function for at least 3 months prior to the study,
  • having any physical or physiological limitation that may affect the ability to perform the tests and physical training,
  • not being able to understand the informed consent form and study procedures.

Arms & Interventions

Low Volume (LV)

Experimental

Participants will be performed 6 sets/week

Intervention: Low volume (LV) (Other)

Moderate Volume (MV)

Experimental

Participants will be performed 18 sets/week

Intervention: Moderate Volume (MV) (Other)

High Volume (HV)

Experimental

Participants will be performed 30 sets/week

Intervention: High Volume (HV) (Other)

Outcomes

Primary Outcomes

Maximum dynamic strength (1RM)

Time Frame: baseline and after 10 weeks of intervention

The one-repetition maximum test will be performed on a bilateral leg extension machine. Briefly, participants will undergo 3 test attempts, interspersed with 5-minute intervals. Loads of 10-15% will be added after each attempt in order to reach the 1RM load within the 3 trials. Participants will be verbally encouraged during each attempt.

Maximum voluntary isometric contraction (MVIC)

Time Frame: baseline and after 10 weeks of intervention

The MVIC test for the leg extension exercise (bilateral) will be performed using an isometric dynamometer (CEFISE Biotechnology, São Carlos, Brazil). Briefly, participants will perform three MVICs at 120º of knee flexion (180º = full extension) lasting 5 s, interspersed with 5 s of rest. Participants will be instructed and verbally encouraged to exert maximum force during all attempts. The highest value obtained for peak and mean torque of the three MVICs will be used for the analysis.

Muscle hypertrophy (thickness)

Time Frame: baseline and after 10 weeks of intervention

Muscle hypertrophy (thickness) of the quadriceps and rectus femoris muscles will be assessed using ultrasound images obtained at 3 anatomical points (30, 50, and 60% of the distance between the greater trochanter of the femur and the knee joint line). Muscle thickness will be analyzed using the image analysis program (ImageJ®).

Secondary Outcomes

  • Rating of perceive exterion (RPE)(Immediately after completion of each set of exercise)
  • Affective responses (pleasure and displeasure)(Immediately after each exercise during training sessions)

Investigators

Sponsor
Universidade Norte do Paraná
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Andreo Fernando Aguiar

Principal Investigator

Universidade Norte do Paraná

Study Sites (1)

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