Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID05976256

Kinesiotaping in Trauma for Acute Shoulder and Chest Wall Injuries Comparing Kinesiotape, Sham Tape, and No Tape Alongside Standard Treatment

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

387

Participants Needed

1

Research Sites

52 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

This research aims to evaluate the effect of kinesiotaping on pain relief in adults with acute traumatic injuries to the shoulder or chest wall. The study compares kinesiotaping, sham taping, and no taping, alongside standard treatment with oral pain medication and a sling for shoulder injuries. It focuses on whether kinesiotaping provides meaningful pain reduction and improves comfort and patient satisfaction compared to placebo or no additional taping. Participants are randomly assigned to one of three groups: kinesiotaping, sham taping without elasticity, or no taping. All groups receive standard care with oral analgesics and a sling if applicable. The study measures pain at multiple time points: 15 minutes, 1 week, 3 weeks, and 8 weeks after treatment. Secondary outcomes include skin reactions, analgesic use, activity levels, patient comfort, satisfaction, and the need for physiotherapy. Patients will be assessed using pain scales and questionnaires at emergency department visits and follow-up intervals. Researchers will monitor pain reduction, skin condition, independence, activity patterns, and satisfaction up to 8 weeks. The study expects no serious complications due to the non-invasive nature of taping and the limited severity of injuries. Participation involves pain evaluations, questionnaires, and monitoring of analgesic use and physiotherapy needs.

CONDITIONS

Brief Title

Kinesiotaping in Trauma

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Acute injury occurred less than 24 hours ago
  • Single shoulder or chest wall injury including rib fracture, AC-joint Tossy type 1 or 2 disruption, minimally displaced clavicle fracture, or minimally displaced proximal humeral fracture
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 involving 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 affected area
  • Skin infection, irritation, or open wound on affected area
  • Does not speak Dutch or English

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants receive one of three treatments: kinesiotaping, sham taping, or no taping, alongside standard treatment with oral analgesics and a sling if they have a shoulder injury.

Visits at 15 minutes, 1 week, 3 weeks, and 8 weeks after treatment start

Trial Site Locations

Total: 1 location

1

Mireille Bakker

Amsterdam, Netherlands, 1090 HM

Actively Recruiting

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Research Team

M

Mireille Bakker, MSc

M

Maro Sandel, MD, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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