- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07495540
Comparison of the Effects of Free Weight and Machine-Based Exercises on Muscular Parameters
March 21, 2026 updated by: Begum Kara Kaya, Biruni University
Comparison of Free Weight and Machine-Based Exercise Effects on Muscular Parameters
The aim of our study is to compare and investigate the effects of resistance exercises performed with free weights and those performed using machine systems on muscular parameters and neuromuscular control.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
26
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Begüm Kara Kaya, PhD
- Phone Number: +905355720021
- Email: bkara@biruni.edu.tr
Study Locations
-
-
Zeytinburnu
-
Istanbul, Zeytinburnu, Turkey (Türkiye), 34015
- Biruni University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being an individual between the ages of 18-30 years
- Being physically inactive according to the International Physical Activity Questionnaire short form (<600 MET-min/week)
- Residing in Istanbul
- Voluntary participation in the study.
Exclusion Criteria:
- Having a neurological or cardiopulmonary system problem that prevents exercise.
- Having mental dysfunction.
- Having an acute musculoskeletal injury which limits exercise participant
- Being pregnant.
- Having answered "YES" to any question on the Exercise Readiness Questionnaire.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Free Weight Resistance Exercise Group
|
Participants will perform supervised resistance exercises using free weights (dumbbells and barbell), including biceps curl, squat, and bench press, at an intensity of 60-80% of one-repetition maximum (1RM), 2 sets of 8-12 repetitions, 3 times per week for 8 weeks.
|
|
Experimental: Machine-Based Resistance Exercise Group
|
Participants will perform supervised resistance exercises using weight machines (including machine-based biceps curl, squat, and bench press) at an intensity of 60-80% of one-repetition maximum (1RM), 2 sets of 8-12 repetitions, 3 times per week for 8 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Strength
Time Frame: 8 weeks
|
Maximal voluntary strength of major muscle groups (upper and lower extremity) will be measured using 1-repetition maximum (1RM) tests for biceps curl, squat, and bench press.
The heaviest weight that can be lifted once with proper form is recorded.
Higher values indicate greater muscle strength.
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscular Endurance - Upper Extremity
Time Frame: 8 weeks
|
Upper extremity endurance will be assessed using the push-up test.
Participants perform as many correct repetitions as possible within 1 minute.
Higher repetitions indicate greater muscular endurance.
|
8 weeks
|
|
Muscular Endurance - Lower Extremity
Time Frame: 8 weeks
|
Lower extremity endurance will be assessed using the squat test.
Participants perform as many correct repetitions as possible in one minute period.
Higher repetitions indicate better muscular endurance.
|
8 weeks
|
|
Neuromuscular Control - Upper Extremity
Time Frame: 8 weeks
|
Upper extremity neuromuscular control will be measured using the Closed Kinetic Chain Upper Extremity Stability Test.
Participants perform hand touches over a marked line in 15 seconds.
The average number of successful touches over 3 trials is recorded; higher scores indicate better neuromuscular control.
|
8 weeks
|
|
Neuromuscular Control - Lower Extremity
Time Frame: 8 weeks
|
Lower extremity neuromuscular control will be measured using the Y-Balance Test.
Participants maintain balance on one leg while reaching with the other leg in three directions (anterior, posteromedial, posterolateral).
Average reach distances over 3 trials are recorded.
Greater distances indicate better neuromuscular control.
|
8 weeks
|
|
Proprioception - Knee Joint
Time Frame: 8 weeks
|
Knee joint position sense will be assessed using digital goniometry at 15° and 60° flexion.
Participants reproduce target angles with eyes closed.
Absolute angular error in degrees is recorded; lower errors indicate better proprioception
|
8 weeks
|
|
Proprioception - Elbow Joint
Time Frame: 8 weeks
|
Elbow joint position sense will be assessed using digital goniometry at 30°, 60°, and 90° flexion.
Absolute angular error is recorded; lower values indicate better proprioception.
|
8 weeks
|
|
Participant Satisfaction and Perceived Change
Time Frame: Post-intervention (after 8 weeks)
|
Global Rating of Change (GROC) scale will be used.
Participants rate perceived improvement after the exercise program on a 7-point numerical scale.
Higher scores indicate greater perceived improvement.
|
Post-intervention (after 8 weeks)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 23, 2026
Primary Completion (Estimated)
May 15, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
March 21, 2026
First Submitted That Met QC Criteria
March 21, 2026
First Posted (Actual)
March 27, 2026
Study Record Updates
Last Update Posted (Actual)
March 27, 2026
Last Update Submitted That Met QC Criteria
March 21, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- St Project
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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