- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05534191
Off-season Training Effects on U19 Soccer Players
Comparison of Functional and Traditional Strength and Power Training on U19 Soccer Players During Off-season in Norway: A Randomized Controlled Trial
The goal of this randomized controlled trial is to evaluate whether functional strength and power training or traditional strength and power training during the off-season can improve soccer-specific performance in trained male U19 Norwegian soccer players.
The main questions it aims to answer are:
Does functional training lead to greater improvements in technical soccer skills (passing, shooting, dribbling) compared to traditional training?
Do both training modalities improve mobility, dynamic balance, sprint speed, change of direction, and jumping performance?
Researchers will compare the functional training group, the traditional training group, and a control group to see if either training approach provides superior performance benefits.
Participants will:
Take part in an 8-week intervention.
Complete two weekly strength sessions (functional or traditional depending on allocation).
Attend two weekly soccer sessions during the first 4 weeks (all groups).
Undergo a standardized test battery measuring mobility, balance, technical skills, sprinting, change of direction, and vertical jump before and after the intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Trøndelag
-
Steinkjer, Trøndelag, Norway, 7714
- SSA Steinkjer
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria
Male soccer players aged 16-20 years.
Active competitors in the Norwegian G19 0. Division or the Norwegian Tipping League (Senior 3. Division).
Minimum of eight years of organized soccer experience.
At least two years of structured resistance training experience.
No concurrent involvement in other structured physical activity programs.
Exclusion Criteria
History of lower-limb injury within the past three months.
Inability to meet the required training attendance (≥14 out of 16 sessions).
Participation in additional structured training programs outside the intervention.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
This group will use a functional training system developed specifically for football players to improve their physical strength and movement abilities on the field.
|
To quantify the effect of a strength intervention for footballers on improved range of motion, balance, speed, jump height, and technical football skills compared to a training group performing basic power exercises and machine-based strength training and a control group.
|
|
Active Comparator: Positive control
This group will use general strength exercises with the purpose of improving physical strength.
|
To quantify the effect of a strength intervention for footballers on improved range of motion, balance, speed, jump height, and technical football skills compared to a training group performing basic power exercises and machine-based strength training and a control group.
|
|
No Intervention: Negative control
Control group A group that is not treated
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Loughborough soccer passing test
Time Frame: Day 1
|
Measure precision in passing (Seconds)
|
Day 1
|
|
Loughborough soccer shooting test
Time Frame: Day 1
|
Measure precision in shooting and reaction (Points and secounds )
|
Day 1
|
|
Agility with ball
Time Frame: Day 1
|
Measure technical abilities with the ball (Seconds)
|
Day 1
|
|
Loughborough soccer passing test
Time Frame: 2 months
|
Measure precision in passing (Seconds)
|
2 months
|
|
Loughborough soccer shooting test
Time Frame: 2 months
|
Measure precision in shooting and reaction (Points and secounds )
|
2 months
|
|
Agility with ball
Time Frame: 2 months
|
Measure technical abilities with the ball (Seconds)
|
2 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic leap balance test
Time Frame: Day 1
|
Measure improved dynamic balance (Secounds)
|
Day 1
|
|
S180 sprinting test
Time Frame: Day 1
|
Measure change of direction abilities (Secounds)
|
Day 1
|
|
Vertical jumping test
Time Frame: Day 1
|
Measure jumping abilities (Cm)
|
Day 1
|
|
Dynamic leap balance test
Time Frame: 2 months
|
Measure improved dynamic balance (Secounds)
|
2 months
|
|
S180 sprinting test
Time Frame: 2 months
|
Measure change of direction abilities (Secounds)
|
2 months
|
|
Vertical jumping test
Time Frame: 2 months
|
Measure jumping abilities (Cm)
|
2 months
|
|
10 m and 20 m linear sprint
Time Frame: Day 1
|
Measure the ability to accelerate and maximum speed (Seconds; Km/h)
|
Day 1
|
|
10 m and 20 m linear sprint
Time Frame: 2 months
|
Measure the ability to accelerate and maximum speed (Seconds; Km/h)
|
2 months
|
|
Active knee extension test
Time Frame: Day 1
|
Measure range of motion (Degrees)
|
Day 1
|
|
Active knee extension test
Time Frame: 2 months
|
Measure range of motion (Degrees)
|
2 months
|
|
Active dorsi flexion test
Time Frame: Day 1
|
Measure range of motion (Degrees)
|
Day 1
|
|
Active dorsi flexion test
Time Frame: 2 months
|
Measure range of motion (Degrees)
|
2 months
|
|
Hip External rotation
Time Frame: Day 1
|
Measure range of motion (Degrees)
|
Day 1
|
|
Hip External rotation
Time Frame: 2 months
|
Measure range of motion (Degrees)
|
2 months
|
|
Hip Internal rotation
Time Frame: Day 1
|
Measure range of motion (Degrees)
|
Day 1
|
|
Hip Internal rotation
Time Frame: 2 months
|
Measure range of motion (Degrees)
|
2 months
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 438956
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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