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Development of a Performance Model for Amputee Football Players

20. september 2026 oppdatert av: Ayşenur Gökşen, Tarsus University

Development and Evaluation of the Effectiveness of a Performance Model for Amputee Football Players

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.

Studieoversikt

Detaljert beskrivelse

Amputee football is a physically and cognitively demanding sport that requires rapid decision-making, attention, visuospatial processing, balance, coordination, and sport-specific motor performance. Therefore, training approaches that simultaneously target cognitive and physical functions may contribute to the performance of amputee football players.

This study aims to investigate the effects of a cognitive game-based exercise program on cognitive and physical performance in amputee football players. The intervention will incorporate structured cognitive game activities into an exercise program to provide simultaneous cognitive and motor stimulation. The activities will involve cognitive demands such as attention, concentration, planning, problem solving, decision-making, and visuospatial processing together with physical tasks.

Participants will undergo baseline assessments of cognitive and physical performance before the intervention. Following completion of the intervention program, the same outcome measures will be repeated to determine changes in cognitive and physical performance. The study will examine whether a structured cognitive game-based exercise approach can improve selected cognitive and physical performance outcomes in amputee football players.

The results may contribute to the development of multidimensional training approaches that integrate cognitive and motor components in amputee football and may provide a basis for future exercise and rehabilitation programs for athletes with lower-limb amputation.

Studietype

Intervensjonell

Registrering (Antatt)

20

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

      • Adana, Tyrkia (Türkiye)
        • Rekruttering
        • Cukurova Unıversty
        • Ta kontakt med:
          • Gonca İnce, Prof
          • Telefonnummer: 0(322) 338 70 0(322) 338 70 01
          • E-post: gince@cu.edu.tr
        • Ta kontakt med:
          • Veysel Alcan, PhD
          • Telefonnummer: 0(322) 338 70 01

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Experimental Arm - Gince Cognitive Game-Based Exercise Group

Participants in this group will receive the Gince cognitive game-based exercise program in addition to their usual amputee football training. The program is designed to improve cognitive and physical performance through structured game-based activities.

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.

Eksperimentell: Control Arm - Usual Training Group:

Participants in this group will continue their usual amputee football training without receiving the Gince cognitive game-based exercise program during the intervention period.

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

Andre navn:
  • Routine Amputee Football Training

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Stroop Test Performance
Tidsramme: 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

Baseline and immediately after completion of the intervention

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Secondary Outcome Measure - Illinois Agility Test Performance
Tidsramme: Baseline and immediately after completion of the intervention

Agility performance will be assessed using the Illinois Agility Test. Completion time will be recorded in seconds. The best performance and mean performance will be recorded.

Time Frame: Baseline and immediately after completion of the intervention

Baseline and immediately after completion of the intervention

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

26. juni 2026

Primær fullføring (Antatt)

2. januar 2028

Studiet fullført (Antatt)

2. februar 2028

Datoer for studieregistrering

Først innsendt

20. september 2026

Først innsendt som oppfylte QC-kriteriene

20. september 2026

Først lagt ut (Faktiske)

25. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

25. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

20. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 125C306
  • 125C306 (Annet stipend/finansieringsnummer: The Scientific and technological research council of Türkiye)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Individual participant data are not planned to be shared due to participant confidentiality and data protection considerations.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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