Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05976256

Kinesiotaping in Trauma

Led by Onze Lieve Vrouwe Gasthuis · Updated on 2025-05-31

387

Participants Needed

1

Research Sites

159 weeks

Total Duration

On this page

Sponsors

O

Onze Lieve Vrouwe Gasthuis

Lead Sponsor

O

OLVG

Collaborating Sponsor

AI-Summary

What this Trial Is About

Rationale: Patients with acute traumatic injury to the shoulder or chest wall in de Emergency Department (ED) usually have intense pain. The patient normally is treated with oral analgesics as standard care and in shoulder injury with a sling. Pain of the shoulder or chest wall increases with movement of the affected arm and chest. Kinesiotaping is offered regularly as an additional pain treatment, but there is no hard evidence about its effectiveness. A randomized pilot study in OLVG (Bakker 2022) showed the pain decreasing more when using kinesiotaping comparing to no tape. However, a placebo-effect could not be ruled out and the pilot data need confirmation in a large cohort of patients to study the effectiveness of additional treatment with kinesiotaping in terms of pain, comfort and patient satisfaction.

CONDITIONS

Official Title

Kinesiotaping in Trauma

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Injury occurred less than 24 hours ago
  • Single injury to shoulder or chest wall including rib fracture
  • Disruption of the acromioclavicular (AC) joint Tossy type 1 or 2
  • Not or hardly displaced fracture of the clavicle
  • Not or hardly displaced fracture of the proximal humerus
Not Eligible

You will not qualify if you...

  • Younger than 18 years
  • Incapacitated persons
  • Refusal to participate
  • Need for intubation
  • Decreased consciousness
  • Hemodynamic instability
  • Three or more rib fractures
  • Rib fractures of ribs 1 to 3
  • Indication for surgery
  • Hospitalization required
  • Presence of haemo- or pneumothorax requiring chest drain
  • Known allergy to adhesive tape
  • Very thin or loose skin on the affected area
  • Skin infection, irritation, or open wound on the affected area
  • Unable to speak Dutch or English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Mireille Bakker

Amsterdam, Netherlands, 1090 HM

Actively Recruiting

Loading map...

Research Team

M

Mireille Bakker, MSc

CONTACT

M

Maro Sandel, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here