- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07425288
Contralateral Effects of Unilateral Isokinetic vs. Single-Leg Squat Training in Sedentary Women
Contralateral Effects of Unilateral Isokinetic vs. Single-Leg Squat Training on Strength, Proprioception, and Muscle Thickness in Sedentary Women: A Randomized Controlled Trial
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ankara
-
Ankara, Ankara, Turkey (Türkiye), 06560
- Gazi University, Faculty of Health Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- female gender,
- no lower extremity problems in the last 6 months,
- not actively participating in sports
Exclusion Criteria:
- history of orthopedic surgery within the last 2 years,
- ongoing lower extremity pain, systemic disease that could prevent exercise,
- a neurological problems.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Unilateral Isokinetic Training
Participants 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 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.
|
|
Experimental: Unilateral Single-Leg Squat Training
Participants in this group will perform unilateral single-leg squat training on one lower extremity only.
The opposite limb will not receive any direct training.
|
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.
|
|
No Intervention: Control Group
Participants in this group will not receive any exercise or training intervention during the study period and will continue their usual daily activities.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Strength
Time Frame: Baseline and after 6 weeks of intervention
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proprioception
Time Frame: Baseline and after 6 weeks of intervention
|
Lower extremity proprioception will be evaluated using joint position sense assessment to determine proprioceptive accuracy in both limbs.
|
Baseline and after 6 weeks of intervention
|
|
Muscle Thickness
Time Frame: Baseline and after 6 weeks of intervention
|
Muscle thickness of selected thigh muscles will be measured using ultrasonography to assess morphological adaptations following unilateral training.
|
Baseline and after 6 weeks of intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 13.11.2023-E.795767 (Other Identifier: gazi university)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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