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Effect of Kinesio Taping After Rotator Cuff Surgery

NCT07375927 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2026-01-29

No results posted yet for this study

Summary

The aim of this study is to evaluate whether postoperative kinesio taping provides additional benefits in pain reduction and functional recovery in patients who have undergone arthroscopic rotator cuff repair.

Patients diagnosed with rotator cuff tear who have undergone surgical treatment will be randomly assigned into two groups. One group will receive standard postoperative rehabilitation together with kinesio taping applied for three weeks, while the control group will receive standard postoperative rehabilitation alone.

Pain levels and shoulder function will be assessed during postoperative follow-up using commonly accepted clinical evaluation scales. The findings of this study are expected to contribute to a better understanding of the role of kinesio taping in the recovery process after rotator cuff surgery.

Conditions

  • Rotator Cuff Tears
  • Shoulder Pain
  • Post Operative Pain

Interventions

OTHER

Kinesio Taping

Application of kinesio taping to the operated shoulder during the postoperative period as an adjunct to standard rehabilitation.

OTHER

Standard Postoperative Rehabilitation

Standard postoperative rehabilitation program following arthroscopic rotator cuff repair.

Sponsors & Collaborators

  • Fatih Sultan Mehmet Training and Research Hospital

    collaborator OTHER

  • Olcay Yavuz

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-28
Primary Completion
2026-08-31
Completion
2026-09-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07375927 on ClinicalTrials.gov