- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06928623
Anxiety in Non-professional Football Players With Recurrent Hamstring Injuries.
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).
Study Overview
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Rubén Cuesta-Barriuso, PhD
- Phone Number: 0034 985103386
- Email: ruben.cuestab@gmail.com
Study Contact Backup
- Name: Rubén Cuesta-Barriuso
- Email: cuestaruben@uniovi.es
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Athletes with an injury, muscular or not, at the time of the study
- Athletes in their first year as registered soccer players.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Observational group
A 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.
|
In the present study, no intervention will be carried out, with the recruited subjects only completing the questionnaires set out in the study variables.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of anxiety
Time Frame: Screening visit
|
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.
|
Screening visit
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of the main sociodemographic variables
Time Frame: Screening visit
|
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)
|
Screening visit
|
|
Measuring the number of hamstring injuries
Time Frame: Screening visit
|
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
|
Screening visit
|
|
Measurement of weekly training load
Time Frame: Screening visit
|
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.
|
Screening visit
|
|
Assessment of the main anthropometric variables
Time Frame: Screening visit
|
In the assessment of the main anthropometric variables, weight (in kg) will be measured.
|
Screening visit
|
|
Measuring the duration of hamstring injuries
Time Frame: Screening visit
|
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
|
Screening visit
|
|
Measurement of the date of the last hamstring injury
Time Frame: Screening visit
|
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
|
Screening visit
|
|
Measurement of the number of seasons that the soccer player has been competing
Time Frame: Screening visit
|
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.
|
Screening visit
|
|
Measurement of the footballer's regular starting position in the team
Time Frame: Screening visit
|
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).
|
Screening visit
|
Collaborators and Investigators
Investigators
- Principal Investigator: Rubén Cuesta-Barriuso, Universidad de Oviedo
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- AnsFut
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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