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Football PlayerNCT06928623

Anxiety in Non-professional Football Players With Recurrent Hamstring Injuries.

An observational study of Football Player, run by Universidad Católica San Antonio de Murcia.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Introduction. Faced with the risk of injury relapse, and as athletes train and compete, they generate anxiety that limits their ability to push themselves to the maximum, influencing their performance. Objectives. Read more about this study

Who is it for?
Ages 18 to 19 years, men onlyHealthy volunteers can take part
Conditions the study is for
Football Player
What is being tested?
Surveys
How many people
88 participants
Where
No sites listed yet
Study dates
10 Apr 2025to 25 May 2025
How long will I take part?
1 Day
Phase
Observational
Are there results?
Not yet: the study is under way

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 19 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Study population: Footballers who will be recruited to the teams Real Murcia, Real Murcia Promesas, Alcantarilla, UCAM, Churra, Guadalupe, all of them belonging to the under-19 category.

Who may be able to join

  • Male athletes aged 18 to 19
  • Registered in the Division of Honor category of the Region of Murcia
  • Who are university students
  • With previous hamstring injuries in the last 12 months.

Who cannot join

  • Athletes with an injury, muscular or not, at the time of the study
  • Athletes in their first year as registered soccer players.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Rubén Cuesta-Barriuso, PhD contact

0034 985103386

ruben.cuestab@gmail.com

Rubén Cuesta-Barriuso contact

cuestaruben@uniovi.es

About this study

Official title: Anxiety in Non-professional Football Players With Recurrent Hamstring Injuries. An Ambispective Cohort Study.

Introduction. Faced with the risk of injury relapse, and as athletes train and compete, they generate anxiety that limits their ability to push themselves to the maximum, influencing their performance.

Objectives. i) To identify the state and trait anxiety of non-professional athletes with previous hamstring injuries; ii) To evaluate the main prognostic factors of anxiety in these athletes; and iii) To analyze the best predictive model of anxiety in soccer players with previous hamstring injuries.

Material and method. Ambispective cross-sectional cohort study. 88 players will be recruited. The primary variable of the study will be anxiety (State-Trait Anxiety Inventory), with the number of recurrences of the study injury being the dependent variable. The secondary variables, estimated as modifying or confounding, will be the main sociodemographic variables (age, type of school/work activity), clinical (number of hamstring injuries, number of relapses of injury in the same location, duration of injury in weeks, date of last injury), sports (weekly training load, seasons competing, regular starting line-up) and anthropometric (weight).

Conditions
Football Player
Being tested
Surveys
Keywords
Football players, Anxiety, Hamstring muscles, Recurrence of injury, Physiotherapy
Medical subject headings
Anxiety Disorders

What participants receive

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

  • SurveysOther

    In the present study, no intervention will be carried out, with the recruited subjects only completing the questionnaires set out in the study variables.

Study groups in NCT06928623
Study groupRoleWhat they receive
Observational groupA single measurement will be taken, and the data will be analyzed anonymously, as the identity of the patients filling in the questionnaires will be unknown to the analyst. The primary variable of the study will be anxiety, with the number of recurrences of the lesion under study being the dependent variable. The secondary variables, estimated as modifying or confounding variables, will be the main clinical, sports, anthropometric and sociodemographic variables.
Receives: Other: Surveys

What is being measured

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

  1. Assessment of anxiety

    Anxiety will be evaluated using the State-Trait Anxiety Inventory. This scale will be used to measure the perception of anxiety of the patients included in the study. The state and trait of anxiety of each subject is evaluated with a score of 0 to 30 points for each scale, where a higher score indicates a higher anxiety index in the trait or state.

    Measured: Screening visit

Secondary outcomes (8)
  1. Assessment of the main sociodemographic variables

    In the evaluation of the main sociodemographic variables, the following will be evaluated: age (in completed months) and type of school/work activity (sedentary/active)

    Measured: Screening visit

  2. Measuring the number of hamstring injuries

    For the data analysis, each subject will be asked to indicate, among the clinical variables, the number of hamstring injuries they have had over the last 3 seasons

    Measured: Screening visit

  3. Measurement of weekly training load

    For the data analysis, each subject will be asked to indicate, among the sports variables, the weekly training load (in hours) that they usually have during the competition stage of the season.

    Measured: Screening visit

  4. Assessment of the main anthropometric variables

    In the assessment of the main anthropometric variables, weight (in kg) will be measured.

    Measured: Screening visit

  5. Measuring the duration of hamstring injuries

    For the data analysis, each subject will be asked to indicate, among the clinical variables, the duration (measured in weeks) of the hamstring injuries they have had over the last 3 seasons

    Measured: Screening visit

  6. Measurement of the date of the last hamstring injury

    For the data analysis, each subject will be asked to indicate, among the clinical variables, the date of the last injury (measured in weeks) to the hamstring muscles over the last 3 seasons

    Measured: Screening visit

  7. Measurement of the number of seasons that the soccer player has been competing

    For the data analysis, each subject will be asked to indicate, among the sports variables, the number of seasons that they have been federated, competing in soccer.

    Measured: Screening visit

  8. Measurement of the footballer's regular starting position in the team

    For the data analysis, each subject will be asked to indicate, among the sporting variables, the footballer's regular starting position in the football team, with a dichotomous answer (yes/no).

    Measured: Screening visit

Timeline

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

  1. First posted15 Apr 2025
  2. Study start10 Apr 2025 (estimated)
  3. Primary completion29 Apr 2025 (estimated)
  4. Study completion25 May 2025 (estimated)

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
Cohort
Time perspective
Cross-sectional
Enrolment
88 participants (estimated)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT06928623
Sponsor's protocol ID
AnsFut
Status last verified
Mar 2025
First submitted
31 Mar 2025
Last updated
15 Apr 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Football Player, run by Universidad Católica San Antonio de Murcia.

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 4 inclusion and 2 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: opening soon, as of the sponsor's last update on 15 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

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?

This study is still under way. Results are not available in the source record yet.

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

Contact Rubén Cuesta-Barriuso, PhD (0034 985103386, ruben.cuestab@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of anxiety (time frame: Screening visit). 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 15 Apr 2025.

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