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Extensor Tendons of Finger AnomaliesNCT07567248

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

A study testing Kinesio Taping in people with Extensor Tendons of Finger Anomalies and Tendon Injuries, run by Pamukkale University at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Kinesio Taping
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
36 participants
Where
1 siteTurkey (Türkiye)
Study dates
7 May 2026to 7 Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

HANDE USTA OZDEMIR, PhD contact

+902582964279

husta@pau.edu.tr

Turkey (Türkiye)1 site
  • Pamukkale University

    Denizli, Kınıklı, 20070

    HANDE USTA OZDEMIR, PhD, +902582964279, husta@pau.edu.tr

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Being tested
Kinesio Taping, Sham Kinesio Taping
Keywords
Extensor tendon, Functional recovery, Extensor lag
Medical subject headings
Hapnes Boman Skeie syndrome, Tendon Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Kinesio TapingOther

    Button-Hole Technique (Affected finger(s)) I-Strip Technique (Support for all metacarpal bones) Supportive Tape Application

  • Sham Kinesio TapingOther

    Sham Button-Hole Technique (Affected finger(s)) Sham I-Strip Technique (Support for all metacarpal bones) Sham Supportive Tape Application

Study groups in NCT07567248
Study groupRoleWhat they receive
Patients in the kinesio taping groupExperimentalPatients 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.
Receives: Other: Kinesio Taping
Patients in the control groupSham comparatorPatients 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.
Receives: Other: Sham Kinesio Taping

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Finger ROM Measurement

    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.

    Measured: Post operative at 12 and 24 weeks

  2. Assessment of Gross Grip and Pinch Strength

    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.

    Measured: Post operative at 12 and 24 weeks

  3. Michigan Hand Outcomes Questionnaire

    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

    Measured: Post operative at 12 and 24 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 May 2026
  2. Study start7 May 2026 (estimated)
  3. Primary completion7 May 2027 (estimated)
  4. Study completion7 Jun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
36 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07567248
Sponsor's protocol ID
E-60116787-020-859084
Status last verified
Apr 2026
First submitted
28 Apr 2026
Last updated
5 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Research data can be shared upon a reasonable request.

Publications

  • Kodak MIH, Ozudogru A, Basat HC, 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 Dec 14:19417381251397956. doi: 10.1177/19417381251397956. Online ahead of print.

    PubMed 41392499
  • Horoz L, Cigdem-Karacay B, Cakmak MF. Effect of Kinesio taping on edema and wrist functions in patients with distal radius fracture followed conservatively with a cast: A randomized controlled single-blinded study. J Hand Ther. 2024 Jul-Sep;37(3):479-488. doi: 10.1016/j.jht.2024.05.003. Epub 2024 Jul 5.

    PubMed 38969599

Questions about this trial

What is this clinical trial studying?

A study testing Kinesio Taping in people with Extensor Tendons of Finger Anomalies and Tendon Injuries, run by Pamukkale University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact HANDE USTA OZDEMIR, PhD (+902582964279, husta@pau.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Finger ROM Measurement (time frame: Post operative at 12 and 24 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07567248, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2026.

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