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Active, not recruitingNCT06831682KT-TKRUpdated Feb 18, 2025

Efficacy of Kinesiotaping During Rehabilitation Following Total Knee Replacement Surgery

An interventional study of Kinesiotaping (KT) and Standard Rehabilitation in Total Knee Replacement, Postoperative Recovery and Rehabilitation Outcome, sponsored by SRH Gesundheitszentrum Bad Herrenalb. Active, not recruiting at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-02-18.

Sponsored by SRH Gesundheitszentrum Bad Herrenalb · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
102
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study was to examine the efficacy of Kinesiotaping (KT) within postoperative rehabilitation after Total Knee Replacement (TKR) surgery by determining whether KT enhances early postoperative outcomes, in terms of reduction of swelling, pain relief and improvement in the function of the knee joint, compared to conventional rehabilitation without the use of KT.

Read the detailed description

Kinesiotaping and Rehabilitation after Total Knee Replacement The effectiveness of Kinesiotaping (KT) in postoperative rehabilitation remains scientifically unproven, despite its widespread use. KT is believed to reduce pain and swelling, improve muscle function, and enhance joint mobility by promoting blood flow and lymphatic drainage. However, high-quality studies assessing its efficacy, particularly following Total Knee Replacement (TKR), are lacking.

Aim of the Study The aim of this study is to demonstrate that KT, when applied during inpatient rehabilitation after TKR, improves clinical outcomes compared to standard rehabilitation without KT.

Specifically, the investigators aim to show that:

KT reduces postoperative swelling and pain, thereby enhancing knee function. KT promotes faster recovery of muscle strength and range of motion. KT shortens the time needed to achieve key postoperative milestones, allowing for a more effective rehabilitation process.

02

Conditions studied

  • Total Knee Replacement
  • Postoperative Recovery
  • Rehabilitation Outcome

Keywords

  • Kinesiotaping
  • Total Knee Replacement
  • Rehabilitation
  • knee joint Function
  • Pain Relief
03

In context

Lead sponsor

SRH Gesundheitszentrum Bad Herrenalb is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adults aged ≥18 years.
  • Patients who have undergone primary Total Knee Replacement (TKR) with uncomplicated wound conditions.
  • No signs of infection post-surgery.
  • Ability to understand study procedures and complete required questionnaires.

Exclusion criteria

Exclusion Criteria:

  • Revision TKR surgeries.
  • Early postoperative complications (e.g., wound healing disorders, deep infections, thrombosis).
  • Severe comorbidities (e.g., heart failure NYHA class 3-4, renal insufficiency grade 3-4, chronic lymphedema, dermatological conditions).
  • Known allergies to Kinesiotaping (KT) or adhesive materials.
  • Neurological or neuromuscular disorders.
  • Cognitive impairments (e.g., dementia) affecting compliance.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
102 participants (estimated)

Study arms

  • Experimental
    Kinesiotaping group

    Patients in this group will receive Kinesiotaping (KT) in addition to standard rehabilitation following TKR surgery. KT will be applied using various techniques, including lymphatic, muscle, and ligament taping.

    Device: Kinesiotaping (KT) · Other: Standard Rehabilitation

  • Active comparator
    Control group (no KT)

    Patients in this group will receive standard rehabilitation following TKR surgery without the application of Kinesiotaping.

    Other: Standard Rehabilitation

Interventions

  • DeviceKinesiotaping (KT)

    Kinesiotaping will be applied using muscle, lymphatic, and ligament taping techniques to promote healing, reduce swelling, and improve muscle function following total knee replacement surgery.

    Also known as: K-Active Tape

  • OtherStandard Rehabilitation

    Patients will receive standard postoperative rehabilitation, including physiotherapy, gait training, and medical exercises, without the application of Kinesiotaping.

06

What researchers measure

Primary outcomes

  1. Pain Level Using the Numeric Rating Scale (NRS)

    Pain Level Using the Numeric Rating Scale (NRS): Pain intensity will be assessed using the Numeric Rating Scale, ranging from 0 (no pain) to 10 (worst possible pain). Unit of Measure: NRS score (0-10), where higher scores indicate worse pain.

    Time frame: From postoperative day 10 to postoperative day 25.

  2. Knee Circumference (Swelling)

    Knee Circumference (Swelling): The circumference of the operated knee will be measured using a standard tape measure at a consistent anatomical location. Unit of Measure: Centimeters.

    Time frame: From postoperative day 10 to postoperative day 25.

  3. Passive Range of Motion (PROM)

    Passive Range of Motion (PROM): Knee joint mobility (flexion and extension) will be measured using a goniometer. Unit of Measure: Degrees.

    Time frame: From postoperative day 10 to postoperative day 25.

Secondary outcomes

  1. Timed Up and Go Test

    Timed Up and Go Test: Measures the time (in seconds) for a patient to rise from a chair, walk 3 meters, turn, and return to the chair. Unit of Measure: Seconds (lower scores indicate better mobility).

    Time frame: From postoperative day 10 to postoperative day 25.

  2. Chair Stand Test

    Chair Stand Test: Measures the number of times a patient can rise from a chair and sit down within 30 seconds. Unit of Measure: Count (higher scores indicate better lower limb strength).

    Time frame: From postoperative day 10 to postoperative day 25.

  3. 10-Meter Walk Test

    10-Meter Walk Test: Measures the time taken to walk 10 meters at a self-selected pace. Unit of Measure: Seconds (lower scores indicate better walking ability).

    Time frame: From postoperative day 10 to postoperative day 25.

07

Study locations

1 site
  • SRH Health Center Bad Herrenalb
    Bad Herrenalb, 76332, Germany
08

References and documents

Individual participant data

Plan to share: Yes — We plan to share de-identified individual participant data that underlie the results reported in the publication, including data on primary and secondary outcomes (e.g., pain levels, knee circumference, range of motion, functional tests). Access to data will be available upon reasonable request to researchers conducting relevant studies. Data will be shared following publication and will be accessible for up to 5 years. Researchers must submit a formal proposal, and data sharing agreements will be required to protect privacy and confidentiality.

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06831682
Lead sponsor
SRH Gesundheitszentrum Bad Herrenalb
Responsible party
Sponsor
First posted
Feb 18, 2025
Start date
Feb 8, 2025
Primary completion
Dec 2025 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Feb 18, 2025

Study contacts

Andreas Veihelmann, MD, PhD
study director · 1 SRH Health-center, Bad Herrenalb, Germany 2 Department of Orthopaedics, Physical Medicine & Rehabilitation, Ludwig-Maximilians- University of Munich, Munich, Germany 3 Department for Spine Therapy, Sports Hospital Stuttgart, Stuttgart, Germany

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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