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

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.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

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.

Study Type

Observational

Enrollment (Estimated)

2

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

      • Gdańsk, Poland
        • Academy of Physical Education in Gdańsk

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

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

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • 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

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Nordic Hamstring Exercise
The 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.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Biodex Balance System
Time Frame: 15 min
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
15 min

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Biodex System
Time Frame: 20 min
The maximum muscle strength of the hamstring group will be assessed for both legs
20 min

Collaborators and Investigators

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

Investigators

  • Study Chair: Magdalena Podczarska-Głowacka, Department of Basic Physiotherapy, Gdansk University of Physical Education and Sport, Gdansk, Poland

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)

July 2, 2024

Primary Completion (Estimated)

August 27, 2024

Study Completion (Estimated)

August 30, 2024

Study Registration Dates

First Submitted

April 18, 2024

First Submitted That Met QC Criteria

April 23, 2024

First Posted (Actual)

April 24, 2024

Study Record Updates

Last Update Posted (Actual)

July 18, 2024

Last Update Submitted That Met QC Criteria

July 17, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • AWFiS/2024_2_P-GM

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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