Contralateral Effects of Unilateral Isokinetic vs. Single-Leg Squat Training in Sedentary Women
1 other identifier
interventional
47
1 country
1
Brief Summary
This randomized controlled trial aims to investigate the contralateral effects of unilateral training in sedentary women. Specifically, the study compares unilateral isokinetic training and single-leg squat training to determine their effects on strength, proprioception, and muscle thickness in both the trained and untrained lower extremities. Participants will be randomly assigned to one of the training groups. The intervention will be applied to one lower limb only. Strength, proprioception, and muscle thickness will be assessed before and after the intervention period. The primary objective is to evaluate whether unilateral training induces cross-education effects in the contralateral limb. The findings of this study may contribute to rehabilitation strategies by clarifying the potential benefits of unilateral exercise programs for improving neuromuscular performance and muscle morphology in sedentary individuals.
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 Nov 2023
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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 15, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 10, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 22, 2024
CompletedFirst Submitted
Initial submission to the registry
February 13, 2026
CompletedFirst Posted
Study publicly available on registry
February 20, 2026
CompletedFebruary 20, 2026
February 1, 2026
5 months
February 13, 2026
February 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Muscle Strength
Muscle strength of the lower extremities will be assessed using isokinetic dynamometry to evaluate peak torque values in both the trained and contralateral limbs.
Baseline and after 6 weeks of intervention
Secondary Outcomes (2)
Proprioception
Baseline and after 6 weeks of intervention
Muscle Thickness
Baseline and after 6 weeks of intervention
Study Arms (3)
Unilateral Isokinetic Training
EXPERIMENTALParticipants in this group will receive unilateral isokinetic strength training applied to one lower extremity only. The contralateral limb will not receive any direct intervention.
Unilateral Single-Leg Squat Training
EXPERIMENTALParticipants in this group will perform unilateral single-leg squat training on one lower extremity only. The opposite limb will not receive any direct training.
Control Group
NO INTERVENTIONParticipants in this group will not receive any exercise or training intervention during the study period and will continue their usual daily activities.
Interventions
Unilateral isokinetic strength training will be applied to one lower extremity using an isokinetic dynamometer. The training program will be performed according to the study protocol. The contralateral limb will not receive any direct intervention.
Participants will perform unilateral single-leg squat exercises on one lower extremity according to the study protocol. The opposite limb will not receive any direct training.
Eligibility Criteria
You may qualify if:
- female gender,
- no lower extremity problems in the last 6 months,
- not actively participating in sports
You may not qualify if:
- history of orthopedic surgery within the last 2 years,
- ongoing lower extremity pain, systemic disease that could prevent exercise,
- a neurological problems.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gazi University, Faculty of Health Sciences
Ankara, Ankara, 06560, Turkey (Türkiye)
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
- SPONSOR INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
February 13, 2026
First Posted
February 20, 2026
Study Start
November 15, 2023
Primary Completion
April 10, 2024
Study Completion
May 22, 2024
Last Updated
February 20, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share