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Hamstring InjuryNCT06382597

Four Weeks of Nordic Hamstring Exercises Impact the Strength and Balance of the Hamstring Muscle Group

An observational study of Hamstring Injury, run by Gdansk University of Physical Education and Sport at 1 site in Poland.

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 aim of the study is to assess the impact of 4 weeks of eccentric Nordic Hamstring Exercise training on changes in the hamstring muscle group, as well as to analyze parameters such as maximum muscle strength of the knee flexors, RFD (rate of force development) and static balance, dynamics for the dominant leg. Read more about this study

Who is it for?
Ages 19 to 26 yearsHealthy volunteers can take part
Conditions the study is for
Hamstring Injury
What is being tested?
Nordic hamstring exercise
How many people
2 participants
Where
1 sitePoland
Study dates
2 Jul 2024to 30 Aug 2024
Phase
Observational
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 19 to 26 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: The study will involve students of the Academy of Physical Education and Sport in Gdańsk, aged 19-26 who practice amateur football.

Who may be able to join

  • healthy people aged 19-26,
  • no injuries,
  • athletes, people practicing sports as amateurs

Who cannot join

  • during the period of greatest training load related to the discipline,
  • overload changes in the joints: knee, hip and lumbar-sacral,
  • pain,
  • muscle fatigue, overtraining,
  • in strength sports a few weeks before the start,
  • inflammation of the osteoarticular and ligamentous elements of the lower limbs,
  • previous injuries, surgical procedures within 6 months before the intervention

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • Academy of Physical Education in Gdańsk

    Gdansk

Other trials in Poland

About this study

The aim of the study is to assess the impact of 4 weeks of eccentric Nordic Hamstring Exercise training on changes in the hamstring muscle group, as well as to analyze parameters such as maximum muscle strength of the knee flexors, RFD (rate of force development) and static balance, dynamics for the dominant leg.

Read the detailed description

Research procedure: Nordic Hamstring Exercise training covers a period of 4 weeks, during which the volunteer exercises 3 times a week for 3 sets, each set consisting of 3 repetitions of NHE. Before starting eccentric exercises, you will warm up for 15 minutes. After each series, there will be a 2-minute passive break, during which the subject will rest. In the first week, the subject will exercise under the supervision of the instructor, in the next three weeks the subject will exercise at home after prior instruction.

Being tested
Nordic hamstring exercise

What participants receive

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

  • Nordic hamstring exerciseOther

    Nordic Hamstring Exercise involves a controlled descent of the upright torso from a vertical kneeling position forward towards the ground (parallel to the ground) and returning to the starting position. The ankle joints are stabilized by the other person's grip during a series of exercises.

Study groups in NCT06382597
Study groupRoleWhat they receive
Nordic Hamstring ExerciseThe subjects will be randomly divided into two research groups. The first research group will undergo a 4-week Nordic Hamstring Exercise training, the second research group will be a control group performing traditional exercises.
Receives: Other: Nordic hamstring exercise

What is being measured

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

  1. Biodex Balance System

    The medial-lateral stability index (MLSI), anteroposterior stability index (APSI) and general static and dynamic stability index will be assessed for both limbs and the dominant leg

    Measured: 15 min

Secondary outcomes (1)
  1. Biodex System

    The maximum muscle strength of the hamstring group will be assessed for both legs

    Measured: 20 min

Timeline

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

  1. First posted24 Apr 2024
  2. Study start2 Jul 2024
  3. Primary completion27 Aug 2024
  4. Study completion30 Aug 2024

Resources

More details

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

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
2 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06382597
Sponsor's protocol ID
AWFiS/2024_2_P-GM
Status last verified
Apr 2024
First submitted
18 Apr 2024
Last updated
19 Sep 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hamstring Injury, run by Gdansk University of Physical Education and Sport at 1 site in Poland.

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 7 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 19 Sep 2024. 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 Poland. 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?

Biodex Balance System (time frame: 15 min). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 19 Sep 2024.

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