- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07517016
Real-Time Pose Recognition Technology for Improving Tennis Learning in Individuals With Intellectual Disabilities
The Impact of Real-Time Pose Recognition Technology on Tennis Learning in Individuals With Intellectual Disabilities: A Comparative Study With Traditional Methods
Study Overview
Status
Intervention / Treatment
Detailed Description
This study was conducted over 14 weeks with 30 participants aged 12-18 years, diagnosed with mild to moderate intellectual disabilities, recruited from special education institutions in Burdur, Turkey. Participants were randomly assigned to two groups: an experimental group receiving tennis training supported by RPRT and a control group receiving traditional face-to-face instruction.
The intervention consisted of three 45-minute sessions per week, with participants practicing forehand, backhand, and serve skills. The experimental group used a MediaPipe-based system that provided real-time visual feedback on movement accuracy, including body pose, hand gestures, and eye tracking (FaceMesh and Iris modules). The control group received conventional instruction with in-person guidance and manual correction from instructors.
Weekly interim assessments monitored skill accuracy, frequency and type of errors, reaction time, attention, and motivation. Primary outcomes included skill performance metrics and reaction times, while motivation and attention were assessed using semi-structured interviews. Data were collected via structured observation forms, video recordings, and interviews, and analyzed using SPSS software with repeated measures ANOVA and paired/independent t-tests.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Burdur
-
Burdur, Burdur, Turkey (Türkiye), 15030
- Burdur Mehmet Akif Ersoy University, Faculty of Sport Sciences
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants must be aged 12-18 years.
- Participants must have a diagnosis of mild to moderate intellectual disability.
- Participants must have similar learning speed and attention span as assessed by screening.
- Participants (or their legal guardians) must provide informed consent.
- Participants were given a mini mental test, and those scoring above 18 were included.
Exclusion Criteria:
- Participants who wish to withdraw from the study at any time.
- Participants who do not regularly attend training sessions; their data will be excluded from analysis.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control Group - Traditional Tennis Training
Participants in this arm will receive conventional face-to-face tennis training from instructors.
Training occurs three times per week, 45 minutes per session, over 14 weeks, following the same movement curriculum (forehand, backhand, serve).
Instructors demonstrate correct techniques, provide manual corrections if necessary, and monitor participant performance.
Sessions are conducted in subgroups of 5 participants.
Weekly assessments include movement accuracy, error frequency/type, reaction time, and attention/motivation levels using semi-structured observation forms.
|
Participants receive conventional tennis instruction from trainers, including demonstrations, manual corrections, and guidance on correct movement execution.
Sessions occur 3 times per week, 45 minutes per session, for 14 weeks, following the same movement curriculum (forehand, backhand, serve).
Weekly assessments include movement accuracy, error frequency/type, reaction time, and attention/motivation levels.
Other Names:
|
|
Experimental: Experimental / RPRS Group
Participants in this arm will receive tennis training supported by RPRS.
During each 45-minute session, held three times per week for 14 weeks, participants perform tennis movements (forehand, backhand, serve) individually while the system provides real-time visual feedback on movement accuracy.
The system records movement correctness, reaction time, and errors, while instructors provide support focusing on the feedback provided by the system.
Group sessions are conducted with 5 participants per subgroup.
Progress is monitored weekly with performance metrics and motivational/attention observations using semi-structured forms.
|
Participants perform tennis movements (forehand, backhand, serve) individually while the RPRS (MediaPipe) system provides real-time visual feedback on movement accuracy, records movement correctness, reaction time, and errors.
Training occurs 3 times per week, 45 minutes per session, for 14 weeks.
Instructors provide guidance focusing on system feedback.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy and Number of Errors in Tennis Movements
Time Frame: 14 weeks, with weekly assessments and post-test
|
Accuracy of forehand, backhand, and serve movements, and the number, type, and frequency of errors will be measured using camera recordings and RPRS.
Evaluations occur at pre-test, weekly interim assessments, and post-test.
|
14 weeks, with weekly assessments and post-test
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Motivation Level During Sessions
Time Frame: Pre-test, week 7, and post-test
|
Participants' self-reported motivation, assessed through semi-structured interviews at pre-test, mid-test, and post-test.
|
Pre-test, week 7, and post-test
|
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Reaction Time in Tennis Movements
Time Frame: 14 weeks, with weekly assessments and post-test
|
Time taken to initiate and complete forehand, backhand, and serve movements.
Measured using the RPRS at pre-test, weekly interim assessments, and post-test.
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14 weeks, with weekly assessments and post-test
|
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Learning Speed in Tennis Movements
Time Frame: 14 weeks, with weekly assessments and post-test
|
Improvement rate in movement accuracy during the 14-week training program.
Calculated from weekly scores and pre-post test results using the RPRS.
|
14 weeks, with weekly assessments and post-test
|
|
Attention Level During Sessions
Time Frame: Pre-test, week 7, and post-test
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Participants' attention during sessions, measured via semi-structured interviews and eye-tracking data at pre-test, mid-test, and post-test.
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Pre-test, week 7, and post-test
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Collaborators and Investigators
Investigators
- Principal Investigator: Elif Top, PhD, Burdur Mehmet Akif Ersoy University, Faculty of Sport Sciences
Publications and helpful links
General Publications
- Johnson, D. (2019). Adaptive Learning Systems and Personalized Education. Perspectives in Innovative Education, 1(1), 1-10.
- He, Q., Chen, H., & Mo, X. (2024). Practical application of interactive AI technology based on visual analysis in professional system of physical education in universities. Heliyon, 10(3).
- Chiu, T. K. (2024). The impact of Generative AI (GenAI) on practices, policies and research direction in education: A case of ChatGPT and Midjourney. Interactive Learning Environments, 32(10), 6187-6203
- Ahuja, N. J., Dutt, S., Choudhary, S. L., & Kumar, M. (2025). Intelligent tutoring system in education for disabled learners using human-computer interaction and augmented reality. International Journal of Human-Computer Interaction, 41(3), 1804-1816.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/1789
- 1183-YL-25 (Other Identifier: Burdur Mehmet Akif Ersoy University Scientific Research Projects Unit (BAP))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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