- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07729085
Effect of Reverse Nordic Exercise on Countermovement in Youth Soccer Players
Preliminary Effects of Reverse Nordic Exercise on Countermovement Jump Performance in Youth Soccer Players: A Pilot Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Murcia
-
Murcia, Murcia, Spain, 30107
- Universidad Católica San Antonio de Murcia
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Between 16 and 18 years old
- Soccer Players
Exclusion Criteria:
- Pathologies or Musculoskeletal Injuries in the last 6 months
- Surgical Interventions in the lower extremities in the last 6 months
Study Plan
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 |
|---|---|
|
Experimental: Experimental: Nordic Reverse Protocol
The intervention group performed the reverse Nordic exercise or quadriceps drop protocol for four weeks in their training sessions. Participants assigned to the intervention group warm up for approximately 15/20 minutes, consisting of five minutes of continuous running at low speed (approximately 10 km/h), followed by 3 minutes of stretching the lower extremities and three separate progressive sprints. between them with two minutes of rest to finish, then they will carry out the corresponding series and repetitions of the protocol and continue with their usual training. |
The participant begins on their knees, with the trunk upright and fully aligned.
At this moment, the soccer player slowly leans back, maintaining the starting position by means of a controlled flexion of the knees.
This fall is executed at the lowest speed possible to maximize muscle load in the eccentric phase and reach the point of maximum flexion.
|
|
No Intervention: No Intervention : Usual Training Sessions
The control group did not have any intervention, the participants randomly assigned to this group continued with their usual training sessions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flight Time
Time Frame: It was performed 3 days after completing the 4-week reverse Nordic exercise protocol.
|
Chronojump Boscosystem® contact platform (Barcelona), to measure the vertical jump (CMJ and Abalakov) and the Chronojump Boscosystem® Software version 1.7.1
|
It was performed 3 days after completing the 4-week reverse Nordic exercise protocol.
|
|
Jump Height
Time Frame: It was performed 3 days after completing the 4-week reverse Nordic exercise protocol.
|
Chronojump Boscosystem® contact platform (Barcelona), to measure the vertical jump (CMJ and Abalakov) and the Chronojump Boscosystem® Software version 1.7.1
|
It was performed 3 days after completing the 4-week reverse Nordic exercise protocol.
|
Collaborators and Investigators
Sponsor
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CE012205
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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