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Repeated-sprint AbilityNCT02674919

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

A study testing Nordic Hamstring in people with Repeated-sprint Ability, run by Hvidovre University Hospital at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 17 to 35 years, men onlyHealthy volunteers can take part
Conditions the study is for
Repeated-sprint Ability
What is being tested?
Nordic Hamstring
Could I receive a placebo?
No, everyone receives an active treatment
How many people
35 participants
Where
1 siteDenmark
Study dates
Feb 2016to Jun 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 17 to 35 years
  • Men only
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Both the intervention and testing included in protocol will be conducted in the facilities of the included football clubs in Copenhagen, Denmark.

    Copenhagen

Other trials in Denmark

About this study

Official 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

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.

Being tested
Nordic Hamstring, Control
Keywords
Repeated-sprint ability, Nordic Hamstring exercise, Eccentric hamstring muscle strength

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nordic HamstringOther

    Also called Hamstring lowers, Nordic lowers, Hamstring Curl

  • ControlOther

Study groups in NCT02674919
Study groupRoleWhat they receive
Nordic HamstringExperimentalThe 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.
Receives: Other: Nordic Hamstring
ControlOtherThe 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.
Receives: Other: Control

What is being measured

The primary outcome is the main question the study is designed to answer.

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

Secondary outcomes (5)
  1. Single sprint times (best sprint time, sprint time during last sprint).

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

  2. Maximal eccentric knee flexor strength measured using Nordbord device

    Measured: 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.

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

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

    Measured: 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.

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Feb 2016 (estimated)
  2. Study startFeb 2016
  3. Primary completionJun 2016
  4. Study completionJun 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
35 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02674919
Sponsor's protocol ID
NHE-2016-LI
Status last verified
Jun 2018
First submitted
2 Feb 2016
Last updated
14 Jun 2018
Results posted
No
Data monitoring committee
No
Individual data sharing
Yes: All individual data regarding primary and secondary outcome measures.

Publications

  • 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.

    PubMed 15387805
  • 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.

    PubMed 29192837

Questions about this trial

What is this clinical trial studying?

A study testing Nordic Hamstring in people with Repeated-sprint Ability, run by Hvidovre University Hospital at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Jun 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02674919, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jun 2018.

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