Acute Effects of Fibular Repositioning Taping on Balance, Jumping, and Sprint Performance
15. juli 2026 opdateret af: Selim Mahmut GÜNAY, Uludag University
The Acute Effect of Fibular Repositioning Taping on Balance, Jumping, and Sprint Performance in Healthy Individuals: A Randomized Controlled Trial
This randomized controlled trial aims to investigate the acute effects of fibular repositioning taping on balance, jumping, and sprint performance in healthy individuals.
Eligible participants are randomly allocated to one of three groups: fibular repositioning taping, sham taping, or control.
Physical performance and dynamic balance are assessed at baseline and after the intervention using functional outcome measures, including jumping tests, a 10-meter sprint test, and the Y Balance Test.
The study is designed to determine whether fibular repositioning taping produces short-term changes in selected performance parameters compared with sham taping and no intervention.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
90
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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-
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Bursa, Tyrkiet (Türkiye)
- Bursa Uludag University
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Healthy individuals
- Age between 18 and 30 years
- Willingness to participate in the study and provide informed consent
- Ability to perform balance, jump, and sprint performance tests
Exclusion Criteria:
- History of lower extremity injury or surgery within the last 6 months
- Presence of acute pain during testing
- Neurological, orthopedic, or vestibular condition that may affect balance or performance
- Previous experience of adverse reaction to taping material
- Refusal to participate or inability to complete the study procedures
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Fibular Repositioning Taping Group
Participants in this group receive fibular repositioning taping applied to the dominant ankle.
Baseline assessments are performed before taping, and outcome measurements are repeated 30 minutes after the intervention.
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Fibular repositioning taping is applied to the dominant ankle using a rigid taping technique intended to support fibular positioning.
Outcome measurements are repeated 30 minutes after the application.
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Sham-komparator: Sham Taping Group
Participants in this group receive a sham taping application with a similar appearance to the fibular repositioning taping but without therapeutic fibular repositioning.
Baseline assessments are performed before taping, and outcome measurements are repeated 30 minutes after the application.
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Sham taping is applied to the dominant ankle with a similar appearance to the active taping application but without therapeutic fibular repositioning or manual correction
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Ingen indgriben: Control Group
Participants in this group receive no taping intervention.
Baseline assessments are performed, and outcome measurements are repeated after a 30-minute waiting period.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Y Balance Test
Tidsramme: Baseline and 30 minutes after the intervention
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Dynamic balance will be assessed using the Y Balance Test.
The composite score will be calculated from reach distances and normalized to limb length.
Higher composite scores indicate better dynamic balance performance.
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Baseline and 30 minutes after the intervention
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Horizontal Jump Test
Tidsramme: Baseline and 30 minutes after the intervention
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Horizontal jump performance will be assessed using the Horizontal Jump Test.
The jump distance will be measured in centimeters from the starting line to the landing point.
Greater distance indicates better horizontal jump performance.
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Baseline and 30 minutes after the intervention
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10-Meter Sprint Test
Tidsramme: Baseline and 30 minutes after the intervention
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Sprint performance will be assessed using the 10-meter sprint test.
The time required to complete the 10-meter sprint will be recorded in seconds.
Shorter times indicate better sprint performance.
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Baseline and 30 minutes after the intervention
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Vertical Jump Test
Tidsramme: Baseline and 30 minutes after the intervention
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Vertical jump performance will be assessed using the Vertical Jump Test.
Jump height will be measured in centimeters.
Greater jump height indicates better vertical jump performance.
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Baseline and 30 minutes after the intervention
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
2. januar 2026
Primær færdiggørelse (Faktiske)
15. maj 2026
Studieafslutning (Faktiske)
15. maj 2026
Datoer for studieregistrering
Først indsendt
29. april 2026
Først indsendt, der opfyldte QC-kriterier
15. maj 2026
Først opslået (Faktiske)
22. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
17. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
15. juli 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 2025/819/15-10
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
Individual participant data will not be made publicly available in order to protect participant privacy and confidentiality.
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