Integrated Training Program On Jump Performance And Knee Valgus In Youth Football Players
NCT ID: NCT07009041
Last Updated: 2025-06-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
90 participants
INTERVENTIONAL
2024-09-15
2024-11-12
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Warm-Up Phases and Neuromuscular Performance
NCT07284706
The Effects of an 8-Week Exer-Genie-Assisted Speed and ABC Drill Training Program on Speed, Hamstring Strength, and Vertical Jump Performance in Female Football Players
NCT07274566
The Effect of Using Medial Longitudinal Arch Supported Insoles on Jumping in Young Football Players
NCT06010420
Acute Impact of Static, Dynamic, and Proprioceptive Exercises on Proprioception, Strength, Balance, and Explosive Power
NCT07320027
Comparison of the Immediate Effects of Lower Extremity Static Stretching Exercises on Vertical Jump
NCT06530407
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
A true experimental design was employed, specifically the pre-test-post-test control group model. Jump tests, including the countermovement jump (CMJ), free-arm countermovement jump (CMJFREE), drop jump (DJ), squat jump (SJ), and horizontal jump, were conducted using the My Jump 2 application. The knee valgus test was performed using the My Jump Lab application, which enables markerless motion analysis by evaluating images recorded by a mobile device. This application provides valuable insights into injury prevention particularly in the lower extremities and supports the assessment of proper execution of technical movements.
The training program included strength, flexibility, and plyometric exercises, designed to reduce muscle strength imbalances while enhancing flexibility and plyometric performance. Since improvements in motor characteristics and muscle balance are expected to positively affect knee valgus angles, all components of the training program were implemented in combination. Strength training was carried out over eight weeks and included full-body, core, and lower extremity exercises. In addition, the anterior cruciate ligament injury prevention program developed by Hewett et al., which emphasizes plyometric training, was incorporated during the first six weeks in accordance with its prescribed duration. Stretching exercises were performed following strength training sessions throughout the entire eight-week period. The training program was administered exclusively to the experimental group and followed a consistent schedule and sequence. Training sessions were conducted three times per week for eight weeks, separate from routine football practices. Plyometric exercises were included once per week, and a minimum one-day rest interval was maintained between sessions.
Data were analyzed using SPSS version 27. The Kolmogorov-Smirnov test was used to assess the normality of data distribution. Repeated Measures Analysis of Variance (ANOVA) was applied for within-subject comparisons, while the Bonferroni test was used to determine the source of significant differences. Between-group comparisons were conducted using the Independent Samples t-test.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental Group
The group that received 8-week training programs
Strength training program
Strength training was implemented for eight weeks, including full-body, core, and leg exercises.
Stretching exercises program
Stretching exercises were performed after strength training for the entire eight-week period. The training was administered exclusively to participants in the experimental group, following a consistent schedule and sequence. The program was conducted three days a week for eight weeks, separate from regular football training.
Plyometric exercises program
Plyometric exercises were included only one day per week, and a minimum one-day rest period was maintained between training sessions.Since this program was originally 6 weeks long, it was implemented in the first 6 weeks of the study's implementation process.
Demographic tests
Demographic tests were applied to determine the height, weight and BMI values for the identification of the participants.
Jump tests
Jump tests (CMJ, CMJ Free, SJ, DJ, Horizontal Jump). Three different measurements were taken at three different times.(Before starting, end of week 4 and after completion of week 8).
Knee Valgus tests
It was conducted to determine the right and left knee valgus values of the participants.Three different measurements were taken at three different times. (Before starting, end of week 4 and after completion of week 8).
Control Group
Group without any intervention
Demographic tests
Demographic tests were applied to determine the height, weight and BMI values for the identification of the participants.
Jump tests
Jump tests (CMJ, CMJ Free, SJ, DJ, Horizontal Jump). Three different measurements were taken at three different times.(Before starting, end of week 4 and after completion of week 8).
Knee Valgus tests
It was conducted to determine the right and left knee valgus values of the participants.Three different measurements were taken at three different times. (Before starting, end of week 4 and after completion of week 8).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Strength training program
Strength training was implemented for eight weeks, including full-body, core, and leg exercises.
Stretching exercises program
Stretching exercises were performed after strength training for the entire eight-week period. The training was administered exclusively to participants in the experimental group, following a consistent schedule and sequence. The program was conducted three days a week for eight weeks, separate from regular football training.
Plyometric exercises program
Plyometric exercises were included only one day per week, and a minimum one-day rest period was maintained between training sessions.Since this program was originally 6 weeks long, it was implemented in the first 6 weeks of the study's implementation process.
Demographic tests
Demographic tests were applied to determine the height, weight and BMI values for the identification of the participants.
Jump tests
Jump tests (CMJ, CMJ Free, SJ, DJ, Horizontal Jump). Three different measurements were taken at three different times.(Before starting, end of week 4 and after completion of week 8).
Knee Valgus tests
It was conducted to determine the right and left knee valgus values of the participants.Three different measurements were taken at three different times. (Before starting, end of week 4 and after completion of week 8).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being a male
* Residing in Kayseri
* Be between 18-19 years old
Exclusion Criteria
* Being a female
* Residence outside Kayseri
* Being outside the 18-19 age range
18 Years
19 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
TC Erciyes University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Vesile Şahiner Güler
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Erciyes University
Talas, None Selected, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ERU-SAGENS-VSG-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.