- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07399548
Effects of 8-Week Plyometric Training on Basketball Performance and Isokinetic Strength (PT-BASKET)
February 6, 2026 updated by: Mustafa Şakir Akgül, Kastamonu University
Effects of Plyometric Training on Linear Sprint, Change-of-Direction, and Isokinetic Strength Performances in Male Basketball Players
This study aims to evaluate the effects of an 8-week plyometric training program on the physical performance of male basketball players.
The research focuses on measuring improvements in linear sprinting speed, change-of-direction (agility) abilities, and vertical jump height.
Additionally, the study examines changes in the participants' muscle strength through isokinetic testing.
Twenty-four trained basketball players were divided into two groups: the control group followed their regular basketball training, while the experimental group added specific plyometric exercises, such as jumps and bounds, twice per week.
By comparing the results before and after the 8-week intervention period, the study seeks to determine if this training method effectively enhances the athletic skills required in competitive basketball.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This randomized controlled trial was designed to investigate the multidimensional effects of a structured plyometric training (PT) intervention on competitive male basketball players.
While vertical jump performance is a common focus in PT research, this study specifically evaluates the transfer of adaptations to sport-specific locomotor tasks and isokinetic muscle strength profiles.Participants (N = 24) were randomly assigned to either an experimental group (EG) or a control group (CG).
Both groups maintained their standard basketball training, including shooting, 3-on-3 games, and defensive drills.
The EG performed an additional 8-week progressive plyometric program twice weekly, consisting of exercises such as box jumps, depth jumps, and bounding, with a total volume ranging from 80 to 140 ground contacts per session.
Training volume was meticulously logged, and an adherence rate of at least 85% was required for inclusion in the final analysis.Performance was evaluated through a comprehensive testing battery conducted pre- and post-intervention under standardized conditions.
The primary outcomes focused on linear sprint speed (25-meter sprint) and change-of-direction (CoD) ability (V-cut test), which are critical for the high-intensity demands of basketball.
Secondary outcomes included vertical jump height measured via countermovement jump (CMJ) with and without arm swing, and isokinetic knee and hip strength assessed at angular velocities of 60 degrees per second and 180 degrees per second.The study hypothesized that the addition of PT would lead to superior gains in sprint and CoD performance compared to basketball training alone.
Furthermore, it aimed to explore whether these performance improvements are accompanied by significant changes in isokinetic torque production.
Data were analyzed using a 2 (Time) x 2 (Group) repeated-measures ANOVA to identify significant interactions.
Normality was verified using Skewness and Kurtosis z-scores, with Winsorization applied to outliers to maintain data robustness.
Study Type
Interventional
Enrollment (Actual)
24
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
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Kastamonu, Turkey (Türkiye), 37150
- Kastamonu University, Faculty of Sports Sciences
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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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Active and licensed male basketball players.
- Age between 18 and 22 years.
- Minimum of 3 years of competitive basketball experience.
- Currently participating in regular team training at least 5 days per week.
- Free from any lower-limb musculoskeletal injuries for at least 6 months prior to the study.
Exclusion Criteria:
- Presence of any acute or chronic injury that limits maximal performance during the study period.
- Concurrent participation in any other external strength or power training programs.
- Failure to attend more than 10 percent of the intervention sessions.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Plyometric Training
Participants in the Experimental Group (EG) followed a structured, progressive 8-week plyometric training (PT) program integrated into their regular basketball routine.
The intervention was administered twice weekly (Tuesdays and Thursdays) with at least 48 hours of recovery between sessions.
The program included vertical, horizontal, and lateral movements such as countermovement jumps (CMJ), box jumps, depth jumps, lateral bounds, and squat jumps.
The volume progressed from 80 ground contacts per session in the first two weeks to 140 ground contacts per session in the final two weeks.
Exercises were performed at maximal effort to maximize the utilization of the stretch-shortening cycle (SSC).
All sessions were supervised by a certified strength and conditioning specialist to ensure proper technique and safety.
This program was performed in addition to their standard technical and tactical basketball drills, which were identical to those performed by the control group.
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The intervention consists of a structured 8-week progressive plyometric training (PT) program designed specifically for competitive basketball players. It is performed twice weekly as a supplement to standard technical and tactical basketball drills.
Other Names:
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No Intervention: Standard Basketball Training
Participants in the Control Group (CG) followed their standard basketball training routine for a duration of 8 weeks.
This arm serves as the baseline to compare the specific effects of the plyometric intervention administered to the experimental group.
The sessions consisted of standard technical and tactical basketball drills, including shooting practice, defensive positioning, offensive sets, and scrimmages (e.g., 3-on-3 or 5-on-5 games).
Participants maintained their regular schedule of five training sessions per week, with each session lasting approximately 90 to 120 minutes.
Participants in this group did not participate in any structured plyometric, strength, or power-based conditioning programs during the study period.
All participants were instructed to maintain their normal nutritional habits and daily physical activities to ensure that no external variables influenced the performance outcomes.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
25-meter Linear Sprint Time
Time Frame: Baseline (Week 0) and Post-intervention (Week 8).
|
Time taken to complete a 25-meter straight-line sprint from a standing start.
This measure evaluates linear speed and explosive acceleration.
The test is conducted on a basketball court using electronic timing gates, with the best time of three trials recorded to ensure data accuracy.
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Baseline (Week 0) and Post-intervention (Week 8).
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V-cut Agility Test Time
Time Frame: Baseline (Week 0) and Post-intervention (Week 8).
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Time taken to complete the V-cut agility test, which requires participants to perform four 25-degree directional changes over a 20-meter distance.
This measure evaluates change-of-direction speed and maneuverability.
The best time of three trials is recorded in seconds using electronic timing gates.
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Baseline (Week 0) and Post-intervention (Week 8).
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Countermovement Jump (CMJ) Height
Time Frame: Baseline (Week 0) and Post-intervention (Week 8).
|
Assessment of explosive lower-body power.
Measured using an Optojump photoelectric system (Microgate, Italy) while participants perform a maximal vertical jump with hands on hips.
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Baseline (Week 0) and Post-intervention (Week 8).
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Isokinetic Peak Torque of Knee Extensors and Flexors
Time Frame: Baseline (Week 0) and Post-intervention (Week 8).
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Maximal concentric muscle strength of the knee extensors and flexors is measured at angular velocities of 60 degrees per second and 180 degrees per second.
Assessments are performed using an isokinetic dynamometer (Isomed 2000, D&R Ferstl GmbH, Germany).
The peak torque value from five maximal repetitions at each speed is recorded.
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Baseline (Week 0) and Post-intervention (Week 8).
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)
December 30, 2025
Primary Completion (Actual)
January 30, 2026
Study Completion (Actual)
January 31, 2026
Study Registration Dates
First Submitted
February 1, 2026
First Submitted That Met QC Criteria
February 6, 2026
First Posted (Actual)
February 10, 2026
Study Record Updates
Last Update Posted (Actual)
February 10, 2026
Last Update Submitted That Met QC Criteria
February 6, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025-2287 (Other Identifier: Kastamonu University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The de-identified individual participant dataset, including performance outcomes (25m sprint, V-cut agility, vertical jump, and isokinetic strength values), will be made available to researchers upon reasonable request.
Interested parties must provide a methodologically sound research proposal and sign a data access agreement.
Requests should be directed to the Principal Investigator at Kastamonu University
IPD Sharing Time Frame
Data will be available starting 6 months after article publication and will remain accessible for up to 36 months.
IPD Sharing Access Criteria
Data will be shared with investigators who provide a methodologically sound proposal to achieve the aims in the approved proposal.
Requests should be directed to the corresponding author.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
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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