NCT07700641

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 27, 2026

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 4, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 15, 2026

Completed
29 days until next milestone

First Posted

Study publicly available on registry

July 14, 2026

Completed
6 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2026

Completed
Last Updated

September 14, 2026

Status Verified

September 1, 2026

Enrollment Period

7 days

First QC Date

June 15, 2026

Last Update Submit

September 9, 2026

Conditions

Keywords

Squat exerciseResistance trainingMuscle strengthMuscle oxygenationExercise physiology

Outcome Measures

Primary Outcomes (1)

  • Muscle Strength (Isomed 2000 Isokinetic Dynamometer)

    Quadriceps muscle strength was assessed using a Isomed 2000 isokinetic dynamometer, which is considered a gold-standard method for evaluating muscle performance. Isokinetic testing measures maximal torque produced by the muscle throughout the range of motion at a constant angular velocity, providing reliable data on muscle function. Knee extension strength were evaluated.

    Baseline and 8 weeks post-intervention

Secondary Outcomes (1)

  • Assessment of Muscle Thickness

    Baseline and 8 weeks post-intervention

Study Arms (2)

Tradional Squat Group

EXPERIMENTAL

Participants performed the tradional squat exercise as part of an 8-week training program.

Other: Tradional Squat Group

Heel-Elevated Squat Exercise

EXPERIMENTAL

Participants performed heel-elevated squat exercise as part of an 8-week training program.

Other: Heel-Elevated Squat Group

Interventions

Participants in the Heel-Elevated Squat Group performed all repetitions with both heels supported on rigid 5-cm wedges. Participants completed an 8-week supervised bodyweight squat program performed twice weekly, with progressive increases in training volume and intensity. Squats were performed to approximately parallel depth, using a controlled \~2-s eccentric phase followed by maximal intended concentric velocity, with 2-min rest intervals between sets.

Heel-Elevated Squat Exercise

Participants completed an 8-week supervised bodyweight squat program performed twice weekly, with progressive increases in training volume and intensity. Squats were performed to approximately parallel depth, using a controlled \~2-s eccentric phase followed by maximal intended concentric velocity, with 2-min rest intervals between sets.

Also known as: Classic Squat Group
Tradional Squat Group

Eligibility Criteria

Age18 Years - 35 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsFemale participants only.
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: A randomized parallel-group design was used. Participants were randomly assigned to one of two squat exercise groups, and each group performed a different squat modality.
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

September 14, 2026

Record last verified: 2026-09

Locations