Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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