- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06565130
Wheelchair Basketball and Attention Training
August 20, 2024 updated by: Sultan Akel, Bezmialem Vakif University
Attention Skills of Wheelchair Basketball Players: Occupational Therapy Intervention
The goal of this interventional study is to evaluate the effect of attention training on performance in wheelchair basketball players. The main question it aims to answer is:
Does attention training have an effect on the performance of wheelchair basketball players? Participants will participate attention training from an occupational therapy perspective.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The attention skills of the athletes will be evaluated with a competition-like designed assessment session.
Then, the planned 10-week intervention program will be carried out as one session per week.
After the intervention program, the evaluation session will be repeated and the results will be recorded.
Then, it will be evaluated whether there is improvement in the attention skills of the athletes.
The results obtained will be important for athletes, coaches and professionals working in this field.
Study Type
Interventional
Enrollment (Actual)
9
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
-
-
-
Istanbul, Turkey, 34025
- Bezmialem Vakif University
-
-
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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Actively active in a regional wheelchair basketball team for at least 6 months.
- Volunteering to participate in the research.
- Being literate.
Exclusion Criteria:
- Having a neurological or cognitive disorder other than a physical disability.
- Being colorblind.
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Attention Skills Training
Intervention plan, which will begin by talking about the importance of attention in sports; It will consist of different tasks that include sub-parameters of attention, such as maintaining attention, shifting attention, focusing attention and splitting attention.
|
Attention skills program planned with occupational therapy principles
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The number of successful shots
Time Frame: 10 week
|
The number of mistakes made during the physical activity and track will be recorded as one.Athletes can make mistakes at any stage of the course (depending on their attention skills).
Each mistake will be considered a numerical unit and will be written as one piece.
|
10 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The time to complete the track and each stage
Time Frame: 10 week
|
The time spent by athletes on each stage of the track and the time it takes to complete the physical activity will be recorded.
These times will be considered as a outcome measures.
|
10 week
|
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)
March 12, 2023
Primary Completion (Actual)
September 20, 2023
Study Completion (Actual)
October 20, 2023
Study Registration Dates
First Submitted
July 24, 2023
First Submitted That Met QC Criteria
August 20, 2024
First Posted (Actual)
August 21, 2024
Study Record Updates
Last Update Posted (Actual)
August 21, 2024
Last Update Submitted That Met QC Criteria
August 20, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2022/286
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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