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The Effect of Kinesio Taping on Hand Functions in Zone V-VI Extensor Tendon Injuries

28. april 2026 opdateret af: HANDE USTA, Pamukkale University

Investigation of the Effect of Kinesio Taping on Hand Functions in Zone V-VI Extensor Tendon Injuries: A Double-Blind Randomized Controlled Clinical Trial

This study aims to investigate the effects of Kinesio Taping (KT) on hand function in patients with Zone V-VI Extensor Digitorum Communis (EDC) tendon injuries following primary repair. Extensor tendon injuries in this region often lead to complications such as adhesion formation, reduced range of motion, extensor lag, and impaired hand function, despite standard rehabilitation approaches. Therefore, additional interventions that may enhance tendon gliding and neuromuscular control are of clinical interest.

In this double-blind randomized controlled trial, patients will be assigned to either a KT group or a sham taping control group. Both groups will receive a standardized postoperative rehabilitation program, while the intervention group will additionally receive KT applications between postoperative weeks 6 and 12. Outcome measures, including range of motion, grip and pinch strength, and functional hand performance, will be assessed at 12 and 24 weeks.

The study seeks to determine whether KT provides additional benefits beyond conventional rehabilitation in improving functional recovery after extensor tendon injuries, addressing an important gap in the current literature.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

36

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

  • Navn: HANDE USTA OZDEMIR, PhD
  • Telefonnummer: +902582964279
  • E-mail: husta@pau.edu.tr

Studiesteder

  • Tyrkiet (Türkiye)
    • Kınıklı
      • Denizli, Kınıklı, Tyrkiet (Türkiye), 20070
        • Pamukkale University
        • Kontakt:

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
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Aged between 18 and 65 years
  • Having an isolated Zone V-VI extensor tendon injury
  • Having undergone primary treatment for the injury

Exclusion Criteria:

  • History of prior surgery on the affected extremity
  • Presence of accompanying neurological, orthopedic, rheumatologic, or metabolic disease in the affected extremity
  • Presence of flexor tendon injury
  • Presence of fractures of the metacarpals, carpal bones, or radius/ulna
  • Presence of an open incision line
  • Delayed wound healing
  • Presence of peripheral nerve injury
  • Presence of replantation or amputation

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Patients in the kinesio taping group
Patients in the kinesio taping group will receive KT application starting at postoperative week 6, after complete discontinuation of splint immobilization. During application, the functional correction technique will be used from the insertion to the origin of the Extensor Digitorum Communis (EDC) muscle, with approximately 25-50% tension applied to the tape. KT applications will be performed twice weekly between postoperative weeks 6 and 12, using three tapes in each session. New tapes will be applied in each session and replaced no later than 3 days after the previous application. Before each taping session, the application area will be properly cleaned. Additionally, patients and their caregivers will be thoroughly informed about hygiene of the application area and proper tape removal. The button-hole technique and I-strip technique will be used.
Andet: Kinesio Taping
Button-Hole Technique (Affected finger(s)) I-Strip Technique (Support for all metacarpal bones) Supportive Tape Application
Sham-komparator: Patients in the control group
Patients in the control group will receive sham taping. The application will begin at postoperative week 6 after complete discontinuation of splint immobilization. In the sham application, all steps of the KT procedure (cutting, placement, and application process) will be mimicked; however, no therapeutic tension will be applied to the tapes. Sham taping will be applied twice weekly between postoperative weeks 6 and 12, using three tapes per session. New tapes will be applied in each session and replaced no later than 3 days after the previous application. Before each application, the taping area will be properly cleaned. Patients and their caregivers will also be thoroughly informed about hygiene and proper tape removal.
Andet: Sham Kinesio Taping
Sham Button-Hole Technique (Affected finger(s)) Sham I-Strip Technique (Support for all metacarpal bones) Sham Supportive Tape Application

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Finger ROM Measurement
Tidsramme: Post operative at 12 and 24 weeks
With the wrist in a neutral position, active flexion and extension movements of the metacarpophalangeal (MCP), proximal interphalangeal (PIP), and distal interphalangeal (DIP) joints will be measured using a metal finger goniometer.
Post operative at 12 and 24 weeks
Assessment of Gross Grip and Pinch Strength
Tidsramme: Post operative at 12 and 24 weeks
Gross grip strength will be measured using a hand dynamometer, and pinch strength will be measured in four different positions (tip, pulp, lateral, and three-point pinch) using a pinch meter (Jamar® Hydraulic Dynamometer-Pinchmeter, Serial No: 1420513), according to the standard measurement protocol of the American Society of Hand Therapists.
Post operative at 12 and 24 weeks
Michigan Hand Outcomes Questionnaire
Tidsramme: Post operative at 12 and 24 weeks
The MHQ was developed to measure health status in patients with hand deformities and assesses how well patients perform their usual activities. Each question is scored on a 5-point Likert scale. The total score is calculated by summing all domain scores and dividing by six. Higher scores indicate better outcomes. The questionnaire will be administered by the researchers through face-to-face interviews using a question-and-answer format
Post operative at 12 and 24 weeks

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Pamukkale University

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

  • Kodak MIH, Özüdoğru A, Basat HÇ, Tuncay F. Early effects of Kinesio taping on clinical outcomes in patients with arthroscopic rotator cuff repair: a double-blind randomized controlled trial. Sports Health. 2025. doi:10.1177/19417381251397956.
  • Horoz L, Cigdem-Karacay B, Cakmak MF. Effect of Kinesio taping on edema and wrist functions in patients with distal radius fracture treated conservatively with a cast: a randomized controlled single-blinded study. J Hand Ther. 2024;37(3):479-488. doi:10.1016/j.jht.2024.05.003.

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)

7. maj 2026

Primær færdiggørelse (Anslået)

7. maj 2027

Studieafslutning (Anslået)

7. juni 2027

Datoer for studieregistrering

Først indsendt

28. april 2026

Først indsendt, der opfyldte QC-kriterier

28. april 2026

Først opslået (Faktiske)

5. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

5. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

28. april 2026

Sidst verificeret

1. april 2026

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • E-60116787-020-859084

Plan for individuelle deltagerdata (IPD)

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UBESLUTET

IPD-planbeskrivelse

Research data can be shared upon a reasonable request.

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