- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06883799
Association of Reaction Time and Sleep Quality in Professional Football Players
March 19, 2025 updated by: Maciej Kochman, University of Rzeszow
Football players need to use their cognitive skills to choose and execute actions in reaction to various stimuli throughout a match and training.
Reaction time (RT), an important component of physical fitness, is a key variable for assessing higher cognitive function in football players.
For athletes, sleep is also a critical factor influencing sports performance and is widely recognized as a key indicator of overall health.
The aim of this study is to assess differences in reaction time and sleep quality as well as the association between these variables in a group of professional football players and a control group.
The study analyzes 40 football players (study group) and 40 healthy, non-trained individuals (control group).
Sleep quality is assessed using the Pittsburgh Sleep Quality Index (PSQI), and reaction times, both simple and complex, are assessed using the AT SMART System reaction speed tester.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
80
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
-
-
-
Rzeszów, Poland
- University of Rzeszow
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Professional football players in the Podkarpackie Voivodeship.
Description
Inclusion Criteria:
- Voluntary, informed written consent to participate in the study
- Minimum of 3 years of experience playing football
- Minimum of 3 training sessions per week
- Age between 18 and 30 years
- No musculoskeletal injuries within the last 6 months
- No disorders or conditions that may affect the study results
Exclusion Criteria:
- Lack of voluntary, informed written consent to participate in the study
- Less than 3 years of experience playing football
- Less than 3 training sessions per week
- Age under 18 or over 30 years
- Presence of musculoskeletal injuries within the last 6 months
- Presence of disorders or conditions that may affect the study results
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 |
|---|---|
|
Football players and healthy
The study analyzed 40 football players (study group)
|
Without intervention
|
|
healthy, non-trained individuals
|
Without intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sleep quality
Time Frame: September 2024
|
Pittsburgh sleep quality questionnaire which contained 10 questions about the quality of sleep from the last 4 weeks.
|
September 2024
|
|
Reaction time
Time Frame: September 2024
|
Reaction speed testing was performed using the AT SMART System reaction speed tester.
The tester comprises four components: a control panel, a set of manual and foot buttons, a light and sound stimulus indicator, and a power supply.
|
September 2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
June 20, 2024
Primary Completion (Actual)
September 25, 2024
Study Completion (Actual)
September 25, 2024
Study Registration Dates
First Submitted
March 12, 2025
First Submitted That Met QC Criteria
March 12, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 19, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 013/04/2024
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
product manufactured in and exported from the U.S.
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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