- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07572201
The Effect of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties
29. april 2026 opdateret af: Kübra Kendal, Okan University
Investigation of the Effects of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties in Young Healthy Individuals
The aim of this study is to investigate the effects of kinesio taping applied to the gastrocnemius muscle on muscle oxygenation, pain pressure threshold, and mechanical properties of the muscle in healthy young individuals.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Individuals meeting the inclusion criteria will be randomly assigned to two groups using block randomization: the Kinesio® tape group (KTG) and the placebo group (PG).
Following assessments, individuals will be assigned to their respective groups and will receive Kinesio® tape application from a physiotherapist.
Assessments will be repeated for all individuals at 1 hour and 36 hours after application.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
50
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Kubra Kendal
- Telefonnummer: +90 530-233-8078
- E-mail: kubra.kendal@okan.edu.tr
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:
- Right lower extremity being dominant,
- Not having suffered a musculoskeletal injury to the lower extremity in the last 3 months
Exclusion Criteria:
- Having any orthopedic, neurological, circulatory, or psychiatric diagnosis,
- Having a history of lower extremity surgery,
- Having an allergy to KT or similar tapes,
- Using muscle relaxants and non-steroidal anti-inflammatory drugs,
- Having received physiotherapy and rehabilitation treatment within the last 3 months.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Kinesio® tape group (KT)
KT will be applied by a certified physiotherapist following standardized procedures.
The skin of the lower leg will be cleaned with alcohol before application.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The tape will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension in the KT group will be between 15-25%, with active stretching of the gastrocnemius muscle by the individual during taping.
|
KT will be applied by a certified physiotherapist following standardized procedures.
The skin of the lower leg will be cleaned with alcohol before application.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The tape will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension in the KT group will be between 15-25%, with active stretching of the gastrocnemius muscle by the individual during taping.
|
|
Placebo komparator: Placebo group
The skin of the lower leg will be cleaned with alcohol before the procedure.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The band will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension will be achieved by leaving the band unstretched.
|
The skin of the lower leg will be cleaned with alcohol before the procedure.
Participants will be positioned prone with their lower extremities fully extended, knees in full extension, and ankles in a neutral position.
The band will be placed along the gastrocnemius muscle, over the calcaneal fat pad, to the distal femur.
Tension will be achieved by leaving the band unstretched.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Oxygenation Analysis of the Gastrocnemius Muscle
Tidsramme: Before the application, at the 1st hour and at the 36th hour of the application
|
Before the application, at the 1st hour and at the 36th hour of the application
|
|
Pain Pressure Threshold
Tidsramme: Before the application, at the 1st hour and at the 36th hour of the application
|
Before the application, at the 1st hour and at the 36th hour of the application
|
|
Analysis of the Mechanical Properties of the Gastrocnemius Muscle
Tidsramme: Before the application, at the 1st hour and at the 36th hour of the application
|
Before the application, at the 1st hour and at the 36th hour of the application
|
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 (Anslået)
15. maj 2026
Primær færdiggørelse (Anslået)
15. juni 2026
Studieafslutning (Anslået)
15. august 2026
Datoer for studieregistrering
Først indsendt
29. april 2026
Først indsendt, der opfyldte QC-kriterier
29. april 2026
Først opslået (Faktiske)
7. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
7. maj 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
29. april 2026
Sidst verificeret
1. april 2026
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- IstanbulOkanUniv
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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-
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