Acute Effects of Different Warm-Up Protocols in Amateur Basketball Players

July 20, 2026 updated by: salih tan, Istanbul Medipol University Hospital

Comparison of the Acute Effects of Different Warm-Up Protocols on Flexibility, Vertical Jump, Agility, and Sprint Performance in Amateur Basketball Players: A Three-Arm Randomized Controlled Trial

Brief Summary This randomized controlled trial will compare the immediate effects of three warm-up protocols on physical performance in male amateur basketball players. A total of 45 licensed basketball players aged 15 to 25 years will be randomly assigned to one of three groups: standard dynamic warm-up, dynamic warm-up followed by classical hold-relax proprioceptive neuromuscular facilitation (PNF) stretching, or dynamic warm-up followed by short-duration self-administered PNF stretching.

The main outcome will be the change in countermovement jump height. Additional outcomes will include flexibility, knee range of motion, squat jump height, 20-meter sprint time, agility, dynamic balance, and perceived exertion. Measurements will be performed before the assigned warm-up protocol, immediately after the protocol, and 15 minutes after the protocol.

The study aims to determine whether short-duration self-PNF stretching can improve flexibility while preserving performance more effectively than classical PNF stretching. Each participant will complete the assigned protocol and all assessments during a single study session.

Study Overview

Detailed Description

This study is designed as a single-center, three-arm, parallel-group, assessor-blinded randomized controlled trial investigating the acute effects of different warm-up and proprioceptive neuromuscular facilitation (PNF) stretching protocols in male amateur basketball players.

Forty-five licensed amateur basketball players aged 15 to 25 years will be enrolled and randomly allocated in a 1:1:1 ratio to one of the following groups:

Standard dynamic warm-up Standard dynamic warm-up followed by classical hold-relax PNF stretching Standard dynamic warm-up followed by short-duration self-administered PNF stretching Randomization will be performed using a computer-generated block randomization sequence prepared by an independent researcher who will not participate in outcome assessment. Group assignments will be concealed in sequentially numbered, opaque, sealed envelopes. The investigator conducting the performance assessments will be blinded to group allocation.

All participants will first perform a standardized dynamic warm-up lasting approximately 10 minutes. The program will include light jogging, high knees, butt kicks, walking lunges, side shuffles, carioca running, multidirectional leg swings, and short progressive acceleration runs.

Participants assigned to the classical PNF group will subsequently receive therapist-administered hold-relax PNF stretching for the hamstrings, quadriceps, gastrocnemius, and hip flexor muscles. Each muscle group will undergo a 6-second submaximal isometric contraction followed by a 20-second passive stretch, repeated three times bilaterally.

Participants assigned to the short-duration self-PNF group will perform supervised self-administered PNF exercises targeting the same muscle groups. Each cycle will include brief agonist or antagonist muscle contractions combined with a short stretching phase. Four repetitions will be completed for each muscle group.

Outcome assessments will be conducted at three time points:

Before the assigned intervention Within the first two minutes after completion of the intervention Fifteen minutes after completion of the intervention The primary outcome will be countermovement jump height, which will be used as an indicator of lower-extremity explosive performance. Secondary outcomes will include squat jump height, 20-meter sprint time, T-test agility performance, Illinois agility performance, Y Balance Test results, sit-and-reach flexibility, active knee flexion range of motion, and perceived exertion.

All interventions and assessments will be completed during a single session lasting approximately 60 to 75 minutes. Testing will be conducted under standardized environmental conditions using the same equipment and assessment order. Participants will be instructed to avoid strenuous exercise before testing and to refrain from alcohol, energy drinks, pre-workout products, and other ergogenic supplements that could influence performance.

The study will examine whether short-duration self-administered PNF stretching can provide flexibility benefits without adversely affecting jump, sprint, agility, and balance performance. The findings may help sports physiotherapists, trainers, and coaches select evidence-based warm-up strategies for amateur basketball players.

Study Type

Interventional

Enrollment (Estimated)

45

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 Contact

  • Name: Mehmet Salih TAN, PhD, : Assistant Professor
  • Phone Number: +90 546 726 68 76
  • Email: mstan@medipol.edu.tr

Study Locations

      • Istanbul, Turkey (Türkiye), 34000
        • Istanbul Medipol University, South Campus
        • Contact:
          • Mehmet Salih TAN
          • Phone Number: +905467266876

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
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male
  • Aged 15-25 years
  • Licensed amateur basketball player
  • Minimum 2 years of basketball experience
  • Basketball training at least 3 days per week
  • No serious lower-extremity injury within the past 6 months
  • No lower-extremity surgery within the past 6 months
  • No acute pain or movement limitation
  • No neurological, vestibular, cardiovascular, or respiratory disorder preventing exercise
  • No strenuous exercise or official competition within the past 48 hours No alcohol consumption within the past 24 hours No caffeine, energy drinks, pre-workout products, or ergogenic supplements on the testing day
  • Written informed consent
  • Parental consent and participant assent for participants younger than 18 years

Exclusion Criteria:

  • Acute lower-extremity muscle, tendon, ligament, or bone injury
  • Knee, hip, or ankle surgery within the past 6 months
  • History of major ligament, meniscal, or Achilles tendon injury
  • Lumbar disc herniation, sciatica, peripheral nerve injury, or neurological disorder
  • Vestibular disorder or balance impairment
  • Hypertension, serious cardiovascular disease, or exercise contraindication
  • Physiotherapy or lower-extremity rehabilitation within the past 3 months
  • Regular structured lower-extremity stretching
  • Acute infection, fever, or poor general health on the testing day
  • Inability to complete the intervention or performance tests

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Standard Dynamic Warm-Up

Arm Description:

Participants will complete a standardized dynamic warm-up lasting approximately 10 minutes. The program will include 3 minutes of light jogging, high knees, butt kicks, walking lunges, side shuffles, carioca running, leg swings in the sagittal and frontal planes, and three 10-meter progressive acceleration runs. No PNF stretching will be performed.

Participants will perform a standardized dynamic warm-up lasting approximately 10 minutes. The protocol will include 3 minutes of light jogging, high knees, butt kicks, walking lunges, side shuffles, carioca running, sagittal and frontal plane leg swings, and three 10-meter progressive acceleration runs. Each dynamic exercise will be performed for approximately 20 to 30 seconds or over two 20-meter repetitions, as appropriate.
Active Comparator: Dynamic Warm-Up Plus Classical PNF
Participants will complete the standardized 10-minute dynamic warm-up followed by therapist-administered classical hold-relax proprioceptive neuromuscular facilitation stretching. The PNF protocol will be applied bilaterally to the hamstrings, quadriceps, gastrocnemius, and hip flexors.
Participants will perform a standardized dynamic warm-up lasting approximately 10 minutes. The protocol will include 3 minutes of light jogging, high knees, butt kicks, walking lunges, side shuffles, carioca running, sagittal and frontal plane leg swings, and three 10-meter progressive acceleration runs. Each dynamic exercise will be performed for approximately 20 to 30 seconds or over two 20-meter repetitions, as appropriate.
After completing the standardized dynamic warm-up, participants will receive therapist-administered hold-relax PNF stretching for the hamstrings, quadriceps, gastrocnemius, and hip flexors. Each muscle will be moved to the maximum pain-free stretch position. The participant will then perform a 6-second isometric contraction at approximately 60% to 70% of maximal voluntary effort, followed by relaxation and a 20-second therapist-assisted passive stretch at the new range limit. Three repetitions will be performed bilaterally for each muscle group, with approximately 30 seconds of rest between muscle groups. The PNF component will last
Experimental: Dynamic Warm-Up Plus Short-Duration Self-PNF
Participants will complete the standardized 10-minute dynamic warm-up followed by a supervised short-duration, self-administered proprioceptive neuromuscular facilitation stretching protocol. The protocol will target the hamstrings, quadriceps, gastrocnemius, and hip flexors bilaterally.
Participants will perform a standardized dynamic warm-up lasting approximately 10 minutes. The protocol will include 3 minutes of light jogging, high knees, butt kicks, walking lunges, side shuffles, carioca running, sagittal and frontal plane leg swings, and three 10-meter progressive acceleration runs. Each dynamic exercise will be performed for approximately 20 to 30 seconds or over two 20-meter repetitions, as appropriate.
After completing the standardized dynamic warm-up, participants will perform a supervised short-duration self-PNF protocol targeting the hamstrings, quadriceps, gastrocnemius, and hip flexors. Each repetition will include a 5-second contraction of the opposing muscle group, a 5-second stretch of the target muscle, and a 5-second contraction of the target muscle. Four repetitions will be completed for each muscle group bilaterally, with approximately 20 seconds of rest between muscle groups. The self-PNF component will last approximately 7 to 8 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Countermovement Jump Height
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Lower-extremity explosive performance will be assessed using the countermovement jump test. Participants will perform three maximal vertical jumps with their hands placed on their hips. Jump height will be recorded in centimeters using a standardized jump measurement system. The highest value from the three attempts will be used. Higher values indicate better jump performance. Change from baseline will be compared among the three intervention groups.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Squat Jump Height
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Explosive lower-extremity performance without a countermovement will be assessed using the squat jump test. Jump height will be recorded in centimeters. Participants will complete three attempts, and the highest value will be used. Higher values indicate better performance.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in 20-Meter Sprint Time
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Linear sprint performance will be assessed over a distance of 20 meters using an electronic timing system. Participants will complete three maximal sprint attempts with approximately 3 minutes of rest between attempts. The shortest completion time will be recorded in seconds. Lower values indicate better sprint performance.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in T-Test Agility Time
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Multidirectional agility and change-of-direction performance will be assessed using the standard T-test agility protocol. Participants will complete three attempts, and the shortest completion time will be recorded in seconds. Lower values indicate better agility performance.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Illinois Agility Test Time
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Agility and rapid change-of-direction performance will be assessed using the Illinois Agility Test. Completion time will be recorded in seconds. The shortest valid completion time will be used for analysis. Lower values indicate better agility performance.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Y Balance Test Composite Score
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Dynamic balance will be assessed using the Y Balance Test in the anterior, posteromedial, and posterolateral directions. Reach distances will be normalized to lower-extremity length, and a composite score will be calculated as a percentage. Higher scores indicate better dynamic balance performance.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Sit-and-Reach Distance
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Posterior-chain flexibility will be assessed using the sit-and-reach test. Participants will complete three attempts, and the greatest reaching distance will be recorded in centimeters. Higher values indicate greater flexibility.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Active Knee Flexion Range of Motion
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Active knee flexion range of motion will be measured bilaterally in the prone position using a universal goniometer. Three measurements will be obtained for each lower extremity, and the highest value will be recorded in degrees. Higher values indicate greater knee flexion range of motion and quadriceps flexibility.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Rating of Perceived Exertion
Time Frame: Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Perceived physical exertion will be assessed using the Modified Borg Rating of Perceived Exertion Scale ranging from 0 to 10. A score of 0 indicates no exertion, whereas a score of 10 indicates maximal exertion. Higher scores indicate greater perceived exertion.
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention

Collaborators and Investigators

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

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 (Estimated)

August 5, 2026

Primary Completion (Estimated)

September 10, 2026

Study Completion (Estimated)

September 20, 2026

Study Registration Dates

First Submitted

July 20, 2026

First Submitted That Met QC Criteria

July 20, 2026

First Posted (Actual)

July 23, 2026

Study Record Updates

Last Update Posted (Actual)

July 23, 2026

Last Update Submitted That Met QC Criteria

July 20, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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