NCT02674919

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2016

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

February 2, 2016

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 5, 2016

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2016

Completed
Last Updated

June 14, 2018

Status Verified

June 1, 2018

Enrollment Period

4 months

First QC Date

February 2, 2016

Last Update Submit

June 13, 2018

Conditions

Keywords

Repeated-sprint abilityNordic Hamstring exerciseEccentric hamstring muscle strength

Outcome Measures

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.

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

Secondary Outcomes (5)

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

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

  • Maximal eccentric knee flexor strength measured using Nordbord device

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

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

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

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

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

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

    Measured prior to the intervention (at week 0)

Study Arms (2)

Nordic Hamstring

EXPERIMENTAL

The Nordic Hamstring group performs a progressive strengthening program (Mjolsnes et al., 2004) comprising of the Nordic Hamstring exercise during a period of 10 weeks. The training load increases from one session per week in week 1 to 3 sessions per week in week 3-10. Number of sets and repetitions progressively increase from 2 to 3 and 5 to 12, respectively. The exercise program is performed in the end of a regular football training session.

Other: Nordic Hamstring

Control

OTHER

The control group are asked not to perform the exercise or any other specific strength training for the hamstring muscles and to continue to play football as usual.

Other: Control

Interventions

Also known as: Hamstring lowers, Nordic lowers, Hamstring Curl
Nordic Hamstring
ControlOTHER
Control

Eligibility Criteria

Age17 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

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

Copenhagen, Denmark

Location

Related Publications (2)

  • Mjolsnes R, Arnason A, Osthagen T, Raastad T, Bahr R. A 10-week randomized trial comparing eccentric vs. concentric hamstring strength training in well-trained soccer players. Scand J Med Sci Sports. 2004 Oct;14(5):311-7. doi: 10.1046/j.1600-0838.2003.367.x.

    PMID: 15387805BACKGROUND
  • Ishoi L, Holmich P, Aagaard P, Thorborg K, Bandholm T, Serner A. Effects of the Nordic Hamstring exercise on sprint capacity in male football players: a randomized controlled trial. J Sports Sci. 2018 Jul;36(14):1663-1672. doi: 10.1080/02640414.2017.1409609. Epub 2017 Dec 1.

Study Officials

  • Lasse Ishøi

    Hvidovre University Hospital. University of Southern Denmark

    PRINCIPAL INVESTIGATOR
  • Per Hölmich

    Hvidovre University Hospital. Aspetar

    STUDY CHAIR
  • Per Aagaard

    University of Southern Denmark

    STUDY CHAIR
  • Kristian Thorborg

    Hvidovre University Hospital

    STUDY CHAIR
  • Thomas Bandholm

    Hvidovre University Hospital

    STUDY CHAIR
  • Andreas Serner

    Hvidovre University Hospital. Aspetar

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PT

Study Record Dates

First Submitted

February 2, 2016

First Posted

February 5, 2016

Study Start

February 1, 2016

Primary Completion

June 1, 2016

Study Completion

June 1, 2016

Last Updated

June 14, 2018

Record last verified: 2018-06

Data Sharing

IPD Sharing
Will share

All individual data regarding primary and secondary outcome measures.

Time Frame
Data are available indefinitely at https://www.dropbox.com/s/8g2hve95csz42zp/IPD.xlsx?dl=0
Access Criteria
No access criteria.

Locations