Acute Effects of Different Warm-Up Protocols in Amateur Basketball Players
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
1 other identifier
interventional
45
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 20, 2026
CompletedFirst Posted
Study publicly available on registry
July 23, 2026
CompletedStudy Start
First participant enrolled
August 5, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
September 10, 2026
Study Completion
Last participant's last visit for all outcomes
September 20, 2026
July 23, 2026
July 1, 2026
1 month
July 20, 2026
July 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Countermovement Jump Height
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 Outcomes (8)
Change in Squat Jump Height
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in 20-Meter Sprint Time
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in T-Test Agility Time
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Illinois Agility Test Time
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
Change in Y Balance Test Composite Score
Baseline, immediately after the intervention (within 2 minutes), and 15 minutes after the intervention
- +3 more secondary outcomes
Study Arms (3)
Standard Dynamic Warm-Up
ACTIVE COMPARATORArm 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.
Dynamic Warm-Up Plus Classical PNF
ACTIVE COMPARATORParticipants 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.
Dynamic Warm-Up Plus Short-Duration Self-PNF
EXPERIMENTALParticipants 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.
Interventions
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.
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
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Medipol University, South Campus
Istanbul, 34000, Turkey (Türkiye)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The investigator performing the physical performance assessments will be blinded to group allocation. Randomization will be conducted by an independent researcher who will not participate in outcome assessment. Group assignments will be concealed using sequentially numbered, opaque, sealed envelopes. Participants and the physiotherapist supervising or administering the warm-up protocols cannot be blinded because of the visible differences between the interventions. Statistical analyses will be performed using coded group labels.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor, Department of Physiotherapy and Rehabilitation
Study Record Dates
First Submitted
July 20, 2026
First Posted
July 23, 2026
Study Start (Estimated)
August 5, 2026
Primary Completion (Estimated)
September 10, 2026
Study Completion (Estimated)
September 20, 2026
Last Updated
July 23, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share