The Effects of PNF Stretching on Anaerobic Power and Motor Performance in Adolescent Male Volleyball Players (PNF-VMVP)

April 11, 2025 updated by: Zarife Pancar

The Effects of Proprioceptive Neuromuscular Facilitation Stretching Exercises on Anaerobic Power and Motor Performance in Adolescent Male Volleyball Players: A Randomized Controlled Trial

This randomized controlled study aimed to examine the effects of proprioceptive neuromuscular facilitation (PNF) stretching exercises on anaerobic power and motor performance in adolescent male volleyball players. Eighteen participants aged 15 to 17 years were randomly assigned to an experimental group and a control group. The experimental group performed PNF stretching exercises three times per week for six weeks, in addition to their regular volleyball training. The control group continued their standard volleyball training without PNF stretching. Outcome measures included anaerobic power, flexibility, balance, speed, push-up, and crunch tests. The study hypothesizes that PNF stretching will improve motor performance indicators in adolescent athletes.

Study Overview

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

Interventional

Enrollment (Actual)

18

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Şehitkamil
      • Gaziantep, Şehitkamil, Turkey, 27350
        • Gaziantep University, Faculty of Sport Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
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.
No Intervention: Control Group
Participants in this group continued with their regular volleyball training without any additional intervention.

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.
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
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

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 20, 2023

Primary Completion (Actual)

March 25, 2023

Study Completion (Actual)

May 30, 2023

Study Registration Dates

First Submitted

April 3, 2025

First Submitted That Met QC Criteria

April 3, 2025

First Posted (Actual)

April 10, 2025

Study Record Updates

Last Update Posted (Actual)

April 16, 2025

Last Update Submitted That Met QC Criteria

April 11, 2025

Last Verified

April 1, 2025

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)?

YES

IPD Plan Description

Individual participant data (IPD) will be shared in an anonymized format. No personally identifiable information will be included. Data will be limited to outcome measures and relevant variables necessary for reproducibility and secondary analyses by qualified researchers upon reasonable request.

IPD Sharing Time Frame

IPD will be available beginning 6 months after publication of the results and will be available for 5 years.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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