The Effect of Different Types of Squat Exercises on Muscle Strength and Muscle Oxygenation
1 other identifier
interventional
40
1 country
1
Brief Summary
The study was conducted using a randomized controlled trial design. Participants who met the inclusion criteria were randomly assigned to either the "Classic Squat Group" or the "Heel-Elevated Squat Group." Both groups completed an 8-week strength training program consisting of three sessions per week, following the resistance exercise principles recommended by the American College of Sports Medicine. The main component of the program was the assigned squat variation. Baseline and post-intervention assessments at 8 weeks were performed according to standardized protocols. Exercise sessions were supervised by an experienced physiotherapist to ensure proper technique and minimize injury risk. Training intensity was progressively increased based on participants' adaptation and one-repetition maximum (1-RM) strength levels.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 4, 2026
CompletedFirst Submitted
Initial submission to the registry
June 15, 2026
CompletedFirst Posted
Study publicly available on registry
July 14, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 20, 2026
CompletedJuly 14, 2026
July 1, 2026
7 days
June 15, 2026
July 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Muscle Oxygenation (Moxy Monitor - NIRS)
Muscle oxygenation was assessed using a near-infrared spectroscopy (NIRS)-based Moxy Monitor. The device was placed on the vastus lateralis muscle of the quadriceps during exercise to continuously and non-invasively record the balance between local oxygen delivery and utilization.
Baseline and 8 weeks post-intervention
Secondary Outcomes (1)
Muscle Strength (Isomed 2000 Isokinetic Dynamometer)
Baseline and 8 weeks post-intervention
Study Arms (2)
Classic Squat Group
EXPERIMENTALParticipants performed the classic squat exercise as part of an 8-week resistance training program.
Heel-Elevated Squat Exercise
EXPERIMENTALParticipants performed heel-elevated squat exercise as part of an 8-week resistance training program.
Interventions
Participants in the Classic Squat Group performed a progressive resistance training program three days per week for a total of eight weeks. The squat exercise was performed with full foot contact maintained on a stable ground surface. Training intensity was prescribed at 70-85% of each participant's one-repetition maximum (1-RM) and was progressively adjusted according to individual adaptation. All training sessions were supervised by a physiotherapist to ensure correct technique and safety.
Participants in the Heel-Elevated Squat Group also completed a progressive resistance training program three days per week for eight weeks. The squat exercise was performed using a 20-degree inclined platform placed under the heels. Training intensity was set at 70-85% of each participant's one-repetition maximum (1-RM) and was progressively increased based on individual performance and adaptation. All sessions were conducted under the supervision of a physiotherapist to maintain proper form and reduce injury risk.
Eligibility Criteria
You may qualify if:
- No musculoskeletal, neurological, or cardiopulmonary conditions that would prevent participation in exercise
- Healthy young adults
- No regular lower extremity training participation in the last 6 months
You may not qualify if:
- History of surgery or serious injury to the knee, hip, or ankle joints within the past year
- Presence of any neurological disorder affecting balance or motor control
- Presence of any cardiovascular or pulmonary disease that contraindicates exercise participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Uskudar University
Istanbul, Istanbul, Turkey (Türkiye)
Related Links
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor (PhD)
Study Record Dates
First Submitted
June 15, 2026
First Posted
July 14, 2026
Study Start
April 27, 2026
Primary Completion
May 4, 2026
Study Completion
July 20, 2026
Last Updated
July 14, 2026
Record last verified: 2026-07