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Completed

NCT Number: NCT02674919

Nordic Hamstring and Repeated-sprint Ability in Football (Soccer) Players

The purpose of the study is to investigate the efficacy of a 10-week intervention, using the Nordic Hamstring exercise, on repeated-sprint ability in male sub-elite football players. The primary outcome measure is total sprint time during 4x6 sprint of 10 meters measured using dual-beam photoelectric cells. Additionally, eccentric knee flexor strength is measured using the Nordbord hamstring strength measure. The hypothesis is that strength training of the knee flexor muscles elicited by the Nordic Hamstring exercise will result in enhanced repetitive sprint-ability expressed as a decrease in total sprint time. Furthermore, baseline data is used to assess to correlation between eccentric hamstring strength and active hamstring flexibility AND sprint performance.

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Key information

Age range

17 year–35 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Both the intervention and testing included in protocol will be conducted in the facilities of the included football clubs in Copenhagen, Denmark.

Copenhagen, Denmark

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Sub-elite Danish football player
  • Age 17-35.
  • Able to participate fully in competitive football activities at the time of testing

Exclusion criteria

  • Hamstring pain resulting in loss of training and matches 2 months prior to study initiation.
  • Specific systematic strength training of the hamstring muscles (>1/week) in the preceding 2 months before study initiation.
  • Specific systematic sprint training (>1/week) in the preceding 2 months before study initiation.
  • Longstanding injury (>6 weeks) in the lower extremities in the preceding 6 months to study initiation.

Treatment and study plan

Nordic Hamstring

Other

Other names: Hamstring lowers, Nordic lowers, Hamstring Curl

Control

Other

Primary outcomes

  1. Total sprint time measured during 4x6 sprints of 10 meters. The sprints are performed every 15s and the sets are separated by 3 minutes of rest.

    Time frame: Measured prior to and after the intervention period (at week 0 & 10)

Secondary outcomes

  1. Single sprint times (best sprint time, sprint time during last sprint).

    Time frame: Measured prior to and after the intervention period (at week 0 & 10)

  2. Maximal eccentric knee flexor strength measured using Nordbord device

    Time frame: Measured prior to and after the intervention period (at week 0 & 10)

  3. Eccentric knee flexor strength endurance measured during 12 repetitions of the Nordic Hamstring exercise using Nordbord device.

    Time frame: Measured prior to and after the intervention period (at week 0 & 10)

  4. Active range of motion of hamstring muscles measured using inclinometer.

    Time frame: Measured prior to and after the intervention period (at week 0 & 10)

  5. Correlation between eccentric hamstring strength and active hamstring flexibility AND sprint performance.

    Time frame: Measured prior to the intervention (at week 0)

Sponsors and collaborators

Lead sponsor

Hvidovre University Hospital

Other

Collaborators

  • Aspetar
  • University of Southern Denmark

Registry information

Official study title

The Efficacy of a 10-week Intervention, Using the Nordic Hamstring Exercise, on Repeated-sprint Ability in Football (Soccer) Players - a Randomized Controlled Trial

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Feb 5, 2016
Registry last updated
Jun 14, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.