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Clinical Trials in Turkey / NCT07517016
Active, not recruiting Not applicable

Real-Time Pose Recognition Technology for Improving Tennis Learning in Individuals With Intellectual Disabilities

NCT07517016 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-10-01
Last updated
2026-04-15

Condition(s) studied

Intellectual Disability, Mild to ModerateAdolescence

Investigational drug(s) / intervention(s)

RPRS Tennis TrainingTraditional Face-to-Face Tennis Training

RPRS Tennis Training: 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.

Traditional Face-to-Face Tennis Training: 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.

Study summary

This study investigates the effect of real-time pose recognition technology on learning tennis skills in individuals with mild to moderate intellectual disabilities. The study compares two training methods: traditional face-to-face tennis instruction and training supported by Real-Time Pose Recognition System (RPRS). Thirty participants aged 12-18 from special education institutions in Burdur, Turkey, were randomly assigned to either the experimental group using the technology or a control group receiving traditional instruction. The study aims to determine whether the use of real-time pose recognition improves tennis skill accuracy, learning speed, attention, and motivation compared to traditional methods.

Eligibility

Sex
ALL
Min age
12 Years
Max age
18 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Burdur Mehmet Akif Ersoy University, Faculty of Sport Sciences Burdur Burdur

More Burdur Mehmet Akif Ersoy University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07517016 on ClinicalTrials.gov ↗ ← All trials in Turkey