- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07320027
Acute Impact of Static, Dynamic, and Proprioceptive Exercises on Proprioception, Strength, Balance, and Explosive Power (SSDSPE-RCT)
Comparison of the Acute Effects of Static Stretching, Dynamic Stretching, and Proprioceptive Exercises on Proprioception, Muscle Strength, Balance, and Explosive Power: A Randomized Controlled Trial.
The purpose of this randomized controlled trial is to compare the acute effects of static stretching, dynamic stretching, and proprioceptive exercises on proprioception, muscle strength, balance, and explosive power in young athletes. The study aims to determine how different stretching and exercise modalities influence short-term performance parameters.
The primary questions this study aims to answer are:
Do static stretching, dynamic stretching, and proprioceptive exercises have different acute effects on proprioception?
Do these interventions cause different changes in muscle strength, balance, and explosive power?
Researchers will compare the static stretching, dynamic stretching, and proprioceptive exercise groups to determine which method produces greater improvements in the measured performance parameters.
Participants will:
Perform one of the three assigned exercise protocols according to a standardized warm-up procedure
Undergo pre- and post-exercise assessments, including:
Proprioception (measured with an isokinetic device)
Muscle strength (measured with an isokinetic device)
Balance (measured with a Y balance test and BESS balance test)
Explosive power (measured with the Sargent Vertical Jump Test)
Study Overview
Status
Conditions
Detailed Description
This randomized controlled trial aims to compare the acute effects of static stretching, dynamic stretching, and proprioceptive exercises on knee joint position sense (proprioception), muscle strength, balance, and explosive power in young male soccer players.
Proprioception, the ability to sense the position and movement of joints, muscles, and tendons, plays a critical role in maintaining joint stability. Proprioceptive exercises are widely used among athletes to enhance performance and reduce injury risk. Stretching exercises, particularly static and dynamic techniques, are commonly integrated into warm-up routines to improve flexibility, joint range of motion, and neuromuscular function. However, direct comparisons of the acute effects of static stretching, dynamic stretching, and proprioceptive exercises remain limited.
In this study, healthy male soccer players aged 14-19 years, with at least five years of competitive experience, no knee pain in the past two months, and no history of knee surgery, will be included. Participants will be randomly assigned (block randomization) into three groups:
Static Stretching Group - A controlled-position protocol targeting the quadriceps, hamstrings, plantar flexors, and dorsiflexors, with specific hold durations.
Dynamic Stretching Group - A repetitive movement protocol for the same muscle groups, with gradual speed increases.
Proprioceptive Exercise Group - A 10-exercise proprioceptive training program performed on a BOSU ball, focusing on lower-limb awareness, postural control, and dynamic balance.
All groups will perform a standardized 10-minute warm-up on a cycle ergometer before their respective protocols.
Assessments will be conducted before and immediately after the intervention:
Knee joint position sense (proprioception) - measured with an ISOMED 2000 isokinetic dynamometer
Muscle strength - isokinetic testing of knee flexors and extensors using the isokinetic device
Static balance - Balance Error Scoring System (BESS) test
Dynamic balance - Y-Balance Test
Explosive power - Sargent Vertical Jump Test
The primary hypothesis is that proprioceptive exercises will produce greater acute improvements in proprioception, balance, and explosive power, while dynamic stretching may yield higher acute gains in muscle strength. Findings from this study are expected to inform evidence-based warm-up and training strategies for young soccer players.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Konya, Turkey (Türkiye)
- Tümosan Konyaspor Facilities
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Playing football for at least 5 years.
- Not experiencing knee pain for the last 2 months.
- No history of knee surgery.
- Practicing for 90 minutes at least 5 days a week.
- Volunteering to participate in the study.
- Being between 14 and 19 years old.
Exclusion Criteria:
- Having experienced knee pain for the last two months.
- Having had knee surgery.
- Not willing to participate.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Proprioception group
The group that received proprioception exercises
|
Proprioceptive Exercise Program
Other Names:
|
|
Experimental: Dynamic tension group
The group that received dynamic stretching exercises
|
Our exercise group where we applied the dynamic stretching protocol
Other Names:
|
|
Experimental: Static tension group
The group that received static stretching exercises
|
Our exercise group where we applied the static stretching protocol
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee Joint Position Sense Error (degrees)
Time Frame: Baseline and 1 day
|
Angular joint position matching error (degrees) measured using the ISOMED 2000 isokinetic dynamometer with passive reproduction of target angles.
|
Baseline and 1 day
|
|
Peak Torque during Knee Extension (Nm)
Time Frame: Baseline and 1 day
|
Peak torque (Nm) during knee extension assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peak Torque during Knee Flexion (Nm)
Time Frame: Baseline and 1 day
|
Peak torque (Nm) during knee flexion assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Total Work during Knee Extension (J)
Time Frame: Baseline and 1 day
|
Total work (J) produced during knee extension assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Total Work during Knee Flexion (J)
Time Frame: Baseline and 1 day
|
Total work (J) produced during knee flexion assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Average Work during Knee Extension (J)
Time Frame: Baseline and 1 day
|
Average work (J) during knee extension assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Average Work during Knee Flexion (J)
Time Frame: Baseline and 1 day
|
Average work (J) during knee flexion assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Maximum Work during Knee Extension (J)
Time Frame: Baseline and 1 day
|
Maximum work (J) during knee extension assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Maximum Work during Knee Flexion (J)
Time Frame: Baseline and 1 day
|
Maximum work (J) during knee flexion assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Average Power during Knee Extension (W)
Time Frame: Baseline and 1 day
|
Average power (W) during knee extension assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Average Power during Knee Flexion (W)
Time Frame: Baseline and 1 day
|
verage power (W) during knee flexion assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Knee Joint Angle at Peak Torque during Extension (degrees)
Time Frame: Baseline and 1 day
|
The knee joint angle (degrees) at which peak torque occurs during knee extension, assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Knee Joint Angle at Peak Torque during Flexion (degrees)
Time Frame: Baseline and 1 day
|
The knee joint angle (degrees) at which peak torque occurs during knee flexion, assessed using the ISOMED 2000 isokinetic dynamometer.
Testing was performed in concentric mode at 60 deg/s.
|
Baseline and 1 day
|
|
Y Balance Test Composite Score (percent)
Time Frame: Baseline and 1 day
|
Dynamic balance performance evaluated using the normalized composite reach score from the Y Balance Test (percent).
|
Baseline and 1 day
|
|
BESS Total Error Score (points)
Time Frame: Baseline and 1 day
|
Static balance performance measured using the Balance Error Scoring System (BESS); higher scores indicate worse balance.
|
Baseline and 1 day
|
|
Vertical Jump Height (cm) - Sargent Test
Time Frame: Baseline and 1 day
|
Explosive lower-limb power measured using the Sargent Vertical Jump Test (cm).
|
Baseline and 1 day
|
Collaborators and Investigators
Investigators
- Study Director: Neslihan ALTUNTAŞ YILMAZ E Dr. Öğr. Üyesi, Doctor, Necmettin Erbakan University
Publications and helpful links
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
- 22817
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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