EFFECT OF RESISTANCE TRAINING VOLUME WITH INERTIAL FLYWHEEL ON MUSCLE ADAPTATIONS IN UNTRAINED MEN
NCT ID: NCT06924060
Last Updated: 2025-08-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
30 participants
INTERVENTIONAL
2025-04-28
2025-07-14
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Flywheel resistance Training (FWRT) was developed to increase overload during the eccentric phase by harnessing the energy generated during the concentric phase and applying it to the eccentric phase. This type of training has shown positive results in several studies, improving strength, hypertrophy, jump performance, aerobic endurance, agility, and running economy.
However, there are still no studies that define how the variables of FWRT should be effectively prescribed. Properly adjusting these variables can optimize muscle adaptations and improve physical fitness and health indices. Therefore, in this study, the number of sets will be evaluated to investigate whether a higher number of sets can lead to greater muscle adaptations.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Resistance Training in Untrained Older Adults
NCT02253615
Effects of Low Intensity, High Intensity Eccentric Resistance Training Associated With Blood Flow Restriction
NCT03601104
Effects of a Strength Training Program in Inertial Machines on Bosco Test in Youth Volleyball Players
NCT06159036
Is Inertial Training More Effective Than Conventional Strength Training?
NCT05672641
Autonomical and Hemodynamic Repercussions on Excentric Resistance in Different Intensities With Blood Flow Restriction
NCT03942510
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Participants will be evaluated at two points during the training program: pre-intervention and post-intervention. Muscle strength of the upper and lower limbs will be assessed through one-repetition maximum (1RM) tests on a knee extension or elbow flexion machine and through maximum voluntary isometric contraction (MVIC), evaluated with a load cell. The muscle thickness of the knee extensors and elbow flexors will be measured using a B-mode ultrasound. Load control will be monitored through the following scales: Total Quality of Recovery (TQR) and Visual Analog Scale for Delayed Onset Muscle Soreness (VAS-DOM), and after each set, by the Subjective Perception of Effort (OMNI-RES). To ensure adequate protein intake, at the end of each training session, participants will receive a dose of Whey Protein, based on data collected from their initial food recall and determined by a nutritionist. Anthropometric evaluation will include the measurement of: a) body mass using an electronic/digital scale with 100g resolution , and b) height using a millimetric stadiometer. The procedures used for body mass and height measurement will follow the protocols based on the measurement standards of the International Society for the Advancement of Anthropometry.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
2 sets group
Group that will perform two sets of each exercise developed during the intervention. The other training variables will be identical (repetitions, moment of inertia, rest intervals between sets and repetitions, rest intervals between workouts, training frequency, number and order of exercises).
Flywheel Resistance Training with two sets
For each training session, 4 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps french press). They will perform 2 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
4 sets group
Group that will perform four sets of each exercise developed during the intervention. The other training variables will be identical (repetitions, moment of inertia, rest intervals between sets and repetitions, rest intervals between workouts, training frequency, number and order of exercises).
Flywheel Resistance Training with four sets
For each training session, 4 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps french press). They will perform 4 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
6 sets arm
Group that will perform six sets of each exercise developed during the intervention. The other training variables will be identical (repetitions, moment of inertia, rest intervals between sets and repetitions, rest intervals between workouts, training frequency, number and order of exercises).
Flywheel Resistance Training with six sets
For each training session, 4 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps french press). They will perform 6 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Flywheel Resistance Training with two sets
For each training session, 4 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps french press). They will perform 2 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
Flywheel Resistance Training with four sets
For each training session, 4 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps french press). They will perform 4 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
Flywheel Resistance Training with six sets
For each training session, 4 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps french press). They will perform 6 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Availability to participate in the research (initial meeting, initial and final tests, data collection);
3. Have not been performing traditional resistance exercises for at least 6 months (untrained subjects);
4. Have no previous experience with inertial flywheel devices;
5. Answer no to all questions on the Physical Activity Risk Questionnaire - PAR-Q;
6. Have no medical contraindication of any kind.
Exclusion Criteria
2. Have uncontrolled chronic diseases;
3. Surgical procedures scheduled during interventions;
4. Do not have the flexibility to adapt their diet to the guidelines offered during collection;
5. Use medications or supplements that may interfere with the result, acting as an intervening variable.
18 Years
35 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Federal University of Vicosa
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Suene Franciele Nunes Chaves
PhD Student
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Osvaldo C Moreira, PhD supervisor
Role: STUDY_DIRECTOR
Federal University of Viçosa
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Federal University at Viçosa
Viçosa, Minas Gerais, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
81740024.5.0000.5153
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.