Effect of Reverse Nordic Exercise on Vertical Jump in Youth Soccer Players

October 12, 2023 updated by: Javier Reina Abellan, Universidad de Murcia

Effect of Reverse Nordic Exercise on Vertical Jump in Youth Soccer Players: Randomized Controlled Trial

BACKGROUNDː The reverse nordic hamstring exercise is developed for the eccentric work of the rectus femoris. After performing Nordic exercise protocol (its original), the relationship between increased eccentric hamstring strength, improvements in sprint capacity and reduced incidence of injuries can be confirmed. The review of evidence, led us propose the relationship and the possible benefits that could exist in the performance of four weeks of reverse nordic exercise protocol and the vertical jump, measured with countermovement jump test (CMJ) on a platform of jump.

METHODSː An open randomized controlled trial was conducted, with an intervention and control group, to which they were randomly assigned. The sample was made of 19 players from the San Antonio de Murcia Catholic University Team in the youth A category, aged between 16 and 18 years old. The experimental group (n=10) performed the reverse nordic hamstring exercise protocol for four weeks, in addition to the usual training that they shared with the control group (n=9). Data collection for the CMJ test was done before starting the protocol and immediately after finishing it for all participants. Statistical analysis was carried out with the SPSS program.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

19

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

    • Málaga
      • Torre del Mar, Málaga, Spain, 29740
        • Lara Sánchez Torres

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

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

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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: 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

This is where you will find people and organizations involved with this 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)

October 1, 2021

Primary Completion (Actual)

March 4, 2022

Study Completion (Actual)

April 4, 2022

Study Registration Dates

First Submitted

October 1, 2023

First Submitted That Met QC Criteria

October 12, 2023

First Posted (Actual)

October 17, 2023

Study Record Updates

Last Update Posted (Actual)

October 17, 2023

Last Update Submitted That Met QC Criteria

October 12, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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