- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06921772
The Effects of PNF Stretching on Anaerobic Power and Motor Performance in Adolescent Male Volleyball Players (PNF-VMVP)
The Effects of Proprioceptive Neuromuscular Facilitation Stretching Exercises on Anaerobic Power and Motor Performance in Adolescent Male Volleyball Players: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This clinical trial investigates the effects of a six-week proprioceptive neuromuscular facilitation (PNF) stretching intervention on motor performance in adolescent male volleyball players. A total of 18 participants with at least 6 months of volleyball training experience were randomly divided into two groups: the experimental group (n=9) and the control group (n=9). The experimental group received PNF stretching exercises in addition to their routine training three times per week for six weeks, while the control group continued only with their routine training.
The main outcome measures were anaerobic power (Margaria-Kalamen Test), flexibility (Sit-and-Reach Test), balance (Flamingo Balance Test), speed (20 m sprint), upper body strength (Push-up Test), and core strength (Crunch Test). Pre- and post-test evaluations were conducted. This study contributes to the growing body of literature on flexibility and functional performance development in adolescent athletes and aims to support evidence-based training practices in sports sciences.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Şehitkamil
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Gaziantep, Şehitkamil, Turkey, 27350
- Gaziantep University, Faculty of Sport Sciences
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male participants
- Aged between 15 and 17 years
- At least 2 years of volleyball training experience
- Voluntarily agreeing to participate in the study
- No recent musculoskeletal injuries (in the last 6 months)
Exclusion Criteria:
- Participants with any diagnosed neurological or cardiovascular disorder
- Current use of performance-enhancing drugs or supplements
- History of lower extremity surgery
- Inability to complete the training or testing sessions
- Failure to provide written informed consent
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: PNF Stretching Group
Participants in this group performed proprioceptive neuromuscular facilitation (PNF) stretching exercises three times per week for six weeks, in addition to their regular volleyball training.
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Proprioceptive Neuromuscular Facilitation (PNF) stretching exercises were applied three times per week for six weeks.
The intervention included contract-relax and hold-relax techniques targeting lower extremity muscle groups, conducted in addition to regular volleyball training.
|
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No Intervention: Control Group
Participants in this group continued with their regular volleyball training without any additional intervention.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anaerobic Power (Margaria-Kalamen Test)
Time Frame: Baseline and after 6-week intervention
|
Anaerobic power will be evaluated using the Margaria-Kalamen test, which measures power output based on the time taken to run up a staircase.
The test will be conducted at baseline and after 6 weeks.
|
Baseline and after 6-week intervention
|
|
Hamstring Flexibility (Sit-and-Reach Test)
Time Frame: Baseline and after 6-week intervention
|
Hamstring flexibility will be measured with the Sit-and-Reach test.
Participants sit on the floor with legs extended and reach forward.
The distance reached is recorded in centimeters.
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Baseline and after 6-week intervention
|
|
Static Balance Performance
Time Frame: Baseline and after 6-week intervention
|
Static balance will be measured by having participants stand on one leg for a defined duration without support.
Performance will be evaluated based on duration of balance and postural stability.
|
Baseline and after 6-week intervention
|
|
Sprint Performance (20-m Sprint Test)
Time Frame: Baseline and after 6-week intervention
|
Speed performance will be measured using the 20-meter sprint test.
Participants will run 20 meters at maximal effort, and the time taken will be recorded in seconds.
|
Baseline and after 6-week intervention
|
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Upper Body Endurance (Push-Up Test)
Time Frame: Baseline and after 6-week intervention
|
Upper body muscular endurance will be evaluated by counting the number of push-ups performed within 30 seconds.
|
Baseline and after 6-week intervention
|
|
Core Endurance (Crunch Test)
Time Frame: Baseline and after 6-week intervention
|
Core endurance will be assessed by counting the number of crunches a participant can perform in 30 seconds.
|
Baseline and after 6-week 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
- GAUN-SBF-PANCAR-05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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