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Hamstring InjuryNCT07735416

Pre- and Post-Training Assessment of Sprint Performance, Agility, Balance and Body Awareness in Football Players Regarding Hamstring Injury

An observational study of Hamstring Injury, run by Health Institutes of Turkey at 1 site in Turkey (Türkiye).

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

Aim of the study is to examine the impact of a history of hamstring injury on athletes by determining and comparing the pre- and post-training levels of sprint performance, agility, dynamic balance, and body awareness in football players with and without a history of hamstring injury. Read more about this study

Who is it for?
Ages 18 to 35 years, men onlyHealthy volunteers can take part
Conditions the study is for
Hamstring Injury
How many people
50 participants
Where
1 siteTurkey (Türkiye)
Study dates
30 Jul 2026to 22 Sep 2026
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 18 to 35 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Study population: Licensed Football Players Aged 18-35 with and without a History of Hamstring Injury

Who may be able to join

  • Being a licensed male football player aged 18-35.
  • Having played football actively for at least 2 years.
  • Having attended training sessions regularly within the last 6 months.
  • Having a history of hamstring injury (n=25).
  • Not having a history of hamstring injury (n=25).
  • Voluntarily agreeing to participate in the study.

Who cannot join

  • Having a current history of a diagnosed musculoskeletal injury in the lower extremities.
  • Having undergone lower extremity surgery within the last 6 months.
  • Having a diagnosis of any neurological, orthopedic, or systemic disorder.
  • Having a diagnosis of any systemic disease affecting balance.
  • Having any significant physical limitations that would prevent the application of the tests.
  • Having a diagnosed psychological disorder that would hinder communication.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Haliç Üniversitesi

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Aim of the study is to examine the impact of a history of hamstring injury on athletes by determining and comparing the pre- and post-training levels of sprint performance, agility, dynamic balance, and body awareness in football players with and without a history of hamstring injury.

Read the detailed description

The aim of this study is to compare sprint performance (10-meter sprint test (10mST) and 30-meter sprint test (30mST)), agility (T-Test of Agility), dynamic balance (Y-Balance Test), and body awareness (Body Awareness Questionnaire) levels in licensed football players with and without a history of hamstring injury, before and after training, in order to reveal the effect of a history of hamstring injury on functional performance and acute fatigue response. Capturing acute changes with pre- and post-training measurements and comparing these between groups with and without a history of injury has the potential to make visible "intra-day/intra-training performance fluctuations" that may be overlooked upon returning to the field. This research study is designed as an observational and cross-sectional evaluation study.

What participants receive

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

Study groups in NCT07735416
Study groupRoleWhat they receive
Group IFootball players with a history of hamstring injury
Group IIFootball players without a history of hamstring injury

What is being measured

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

  1. Sprint Performance (10-meter and 30-meter Sprint Tests)

    To evaluate the acceleration and maximum sprint performance of the football players, 10-meter and 30-meter sprint tests will be conducted. The 10-meter sprint test will be used to assess acceleration and explosive power capacity over short distances. Participants will stand in a semi-prone position behind the starting line and will begin a 10-meter run at maximum speed upon receiving the starting command. The time will be recorded in seconds. The 30-meter sprint test will be used to evaluate maximum running speed, sprint performance, and anaerobic capacity. Similarly, participants will begin a 30-meter run at maximum speed upon receiving the starting command. The time will be recorded in seconds.

    Measured: Before and immediately after training

  2. T-Test of Agility

    This test will be administered to assess participants' agility, speed of change of direction, coordination, and reaction capacity. The test course is arranged in a 'T' shape using cones, with 10 meters forward from the starting point and 5 meters to the right and left. Participant runs forward from the starting point to the midpoint, then moves sideways to the right and left as quickly but steadily as possible, and finally runs back to the starting point. The test duration is recorded in seconds using a stopwatch. Shorter test times indicate a higher level of agility and neuromuscular control.

    Measured: Before and immediately after training

  3. Y Balance Test

    The YBT requires the athlete to balance on one leg whilst simultaneously reaching as far as possible with the other leg in three separate directions: anterior, posterolateral, and posteromedial. Therefore, this test measures the athlete's strength, stability and balance in various directions. The YBT composite score is calculated by summing the three reach directions and normalising the results to the lower limb length.

    Measured: Before and immediately after training

  4. Body Awareness Questionnaire (BAQ)

    BAQ is an 18-item self-report scale designed to measure how attentive you are to normal, non-emotional internal bodily processes. It evaluates your sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions. Typically takes about 3 to 5 minutes. Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived conKdence and accuracy in monitoring your physical state over time.

    Measured: Before and immediately after training

Timeline

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

  1. First posted30 Jul 2026
  2. Study start30 Jul 2026
  3. Primary completion22 Sep 2026
  4. Study completion22 Sep 2026

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
Cross-sectional
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07735416
Sponsor's protocol ID
ETurkmen0226
Status last verified
Jul 2026
First submitted
24 Jul 2026
Last updated
23 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hamstring Injury, run by Health Institutes of Turkey at 1 site in Turkey (Türkiye).

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 6 inclusion and 6 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 23 Sep 2026. 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 Turkey (Türkiye). 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?

Sprint Performance (10-meter and 30-meter Sprint Tests) (time frame: Before and immediately after training). The study lists 4 primary outcomes in all. 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 23 Sep 2026.

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