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Clinical Trials in Turkey / NCT07840781
Recruiting Not applicable

Development of a Performance Model for Amputee Football Players

NCT07840781 · tracked via the Priya Life Science Turkey tracker
Sponsor
Tarsus University
Phase
Not applicable
Started
2026-06-26
Last updated
2026-09-25

Condition(s) studied

Cognitive GamesSports PerformanceLower Limb Amputation

Investigational drug(s) / intervention(s)

Gince Intelligence Game-Based Exercise ProgramRoutine Training Group

Gince Intelligence Game-Based Exercise Program: The intervention consists of a 10-session cognitive game-based exercise program using the Gince Intelligence Game. The program is administered in addition to routine amputee football training and is designed to stimulate cognitive and physical performance through game-based activities.

Routine Training Group: Participants will continue their usual amputee football training program throughout the study period without receiving the additional Gince Intelligence Game-based exercise intervention.

Study summary

This study aims to investigate the effects of a cognitive game-based exercise program on cognitive and physical performance in amputee football players. Participants will complete a structured exercise program incorporating cognitive game activities designed to simultaneously stimulate cognitive and motor functions. Cognitive and physical performance outcomes will be assessed before and after the intervention. The findings are expected to provide evidence regarding the potential benefits of integrating cognitive game-based activities into exercise and rehabilitation programs for amputee football players.

Eligibility

Sex
MALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: Individuals with lower-limb amputation who actively participate in amputee football Regular participation in amputee football training Ability to understand and follow the study instructions Voluntary agreement to participate in the study Exclusion Criteria: Presence of an acute musculoskeletal injury that prevents participation in training or performance tests Presence of a medical condition that prevents safe participation in exercise or performance testing Inability to complete the cognitive or physical performance assessments Withdrawal from the study or failure to complete the intervention program

Primary outcome measure(s)

  • Stroop Test Performance — Baseline and immediately after completion of the intervention
    Cognitive inhibitory control and selective attention will be assessed using the Stroop Test. Completion time will be recorded in seconds, and the number of errors will also be recorded. Changes from baseline to post-intervention will be evaluated

Trial sites (1)

FacilityCityRegionStatus
Cukurova Unıversty Adana Turkey (Türkiye) Recruiting

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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 NCT07840781 on ClinicalTrials.gov ↗ ← All trials in Turkey