- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03526393
Construction of the Training Mode Adjustable Equipment Sitting Volleyball
May 17, 2018 updated by: Silvia Regina M. S. Boschi, University of Mogi das Cruzes
The individual adapted sport modalities concentrate most of the technological development for equipment and auxiliary devices, the collective modalities need implements that aid in the development of training and the game.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The individual adapted sport modalities concentrate most of the technological development for equipment and auxiliary devices, the collective modalities need implements that support, in the development of training and the game.
It was developed equipment to assist in the training of technical fundamentals and to improve the efficiency of the motor gesture required for the practice of sitting volleyball in athletes with physical disabilities.
Ten athletes, sitting volleyball players, were selected to perform a set of technical fundamentals and their variations.
Lift the ball (with two variations), attack and serve, and reception.
After the analysis of the movements the equipment was elaborated and constructed based on the measurements made with the athletes, such as contact height with the ball, perimeter, speed and parabola.
Study Type
Interventional
Enrollment (Actual)
10
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
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São Paulo
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Mogi das Cruzes, São Paulo, Brazil, 08780-911
- Silvia Regina Matos da Silva Boschi
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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
18 years to 46 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Have functional classification in national or international level,
- Practice experience of sitting volleyball mode of at least five years
- Participate in weekly training at least three times a week.
Exclusion Criteria:
- Non-acceptance of the athlete to participate in the survey
- Does not have the functional classification for the practice of sport
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: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Support Equipment
Were selected high performance athletes with various kinds of disabilities found in sitting volleyball functional classification.
Three equipment was built to aid high-performance athletes.
All the volunteers tested the survey training equipment, attack and serve training equipment and pass training equipment The motor sign captured footage of each athlete, lasted 30 minutes and the data collected provided the data for the construction of the equipment, later there was the interaction of the athletes with the equipment ready to test effectiveness.
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The survey was checking the equipment designed to assist the lifter training survey with greater precision, in aspects of average height of contact of the ball by striker and maximum perimeter of contact with the ball, for the execution of the attack.
The attack and serve training equipment was designed to assist the athlete in their body positioning for the execution of the fundamentals of the attack and serve, and the correct extension execution of the of trunk, upper limbs and reaction time of contact with the ball.
The equipment for the training of the pass, it was designed to represent the serve forced and technical, variables height, circumference and average speed of the ball.
This equipment has been adapted from the conventional volleyball serve equipment, respecting the limits of the sitting volleyball court.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Ball lifting
Time Frame: 10 minutes
|
The survey training equipment helps the athlete to train precision of gesture engine to the trajectory of the ball is more effective and can get in the best conditions to the attacker.
150 repetitions were performed, with 15 seconds interval between tests.
Unit of measurement: meter (m) and centimeter (cm)
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10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attack and loot
Time Frame: 10 minutes
|
Equipment for training and assists the athlete on the body positioning during the maximal extension from the execution the fundamentals, for the most suitable length of the trunk and upper limbs.
150 repetitions were made to attack and plunder with 15 seconds interval between tests.
Unit of measurement: meter (m) and centimeter (cm).
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10 minutes
|
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Pass training
Time Frame: 15 minutes
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The equipment for training the pass was constructed to perform the trajectory of the ball with respect to height, speed and parabola.
150 repetitions were performed for the equipment, with 15 seconds interval between tests.
Unit of measurement: kilometers per hour (km/h).
|
15 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Silvia R Boschi, PhD, University of Mogi das Cruzes
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)
August 16, 2015
Primary Completion (Actual)
March 21, 2016
Study Completion (Actual)
March 21, 2016
Study Registration Dates
First Submitted
April 28, 2018
First Submitted That Met QC Criteria
May 3, 2018
First Posted (Actual)
May 16, 2018
Study Record Updates
Last Update Posted (Actual)
May 22, 2018
Last Update Submitted That Met QC Criteria
May 17, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- CAEE: 45887715.3.0000.5497
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.