- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03233685
Visual Training and and Reaction Time in Tennis
May 2, 2018 updated by: Matteo Bonato, University of Milan
Effect of Visual Training on Reaction Time and Timing in Tennis Players
Tennis is situational sport in which the result of the game is directly influenced by the interaction with the opponent.
In fact, athletes have to respond in a short-time period to change the way of playing by fast analyzing speed, rotation and direction of the tennis ball.
Therefore, it is extremely complicated to predict exactly what will happen during games and matches.
According to literature goof visual skills, players can receive and process information quickly and can optimize the performance with extreme precision and dexterity.
For this reason, visuomotor training aims to improve reaction times, but its efficiency during playing tennis has not yet been investigated.
Therefore, the aim of this study is to investigate how this training method could affect the improvement of visuomotor performance in young people between 12 and 18 years old.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Two armed, parallel group, randomized control trial.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
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
-
-
Italia
-
Milano, Italia, Italy, 20123
- Universita degli Studi di Milano
-
-
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
12 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age ≥12 years old.
- Playing career of 4 years.
Exclusion Criteria:
- Serious injury in the 6 mouth before the study.
- Subject that already took part to a visual training
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
Subjects will perform a visual training for 12 weeks
|
The visual training will be performed 3 times a week for 40 minutes, at the end of warm up and before the technique training.
The subjects will be performed a progression of exercise to improve their visual ability, their velocity of interpretation and transformation.
The training will be performed with specific panels approved for visual training (S.V.T.A., Torino, Italy).
|
|
Active Comparator: Control Group
Subjects will perform the normal training routine for 12 weeks
|
Normal training routine
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reaction Time
Time Frame: After 12 weeks of training
|
Stroop test
|
After 12 weeks of training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Analysis of tennis skills
Time Frame: After 12 weeks of training
|
QLIPP-TM
|
After 12 weeks of training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Matteo Bonato, Ph.D., University of Milan
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)
October 1, 2017
Primary Completion (Actual)
October 2, 2017
Study Completion (Actual)
January 31, 2018
Study Registration Dates
First Submitted
July 25, 2017
First Submitted That Met QC Criteria
July 25, 2017
First Posted (Actual)
July 31, 2017
Study Record Updates
Last Update Posted (Actual)
May 3, 2018
Last Update Submitted That Met QC Criteria
May 2, 2018
Last Verified
May 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Visual Training
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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