Kinesiotaping in Trauma

Objective: The primary aim of this study is to evaluate the effect of kinesiotaping on number of patients with clinically meaningful pain reduction after 1 week in patients with acute traumatic injury in shoulder or chest wall, compared to sham tape and no tape. The secondary aims are to assess the effect of kinesiotaping on pain reduction at 15 min, 3 weeks and 8 weeks, and the effects on the skin, use of oral analgesics, independence, activity pattern, progress of pain symptoms, comfort and patient satisfaction at 1, 3 and 8 weeks. Also the need of physiotherapy is one of the secondary aims.

Study design: Parallel randomized controlled trial with three arms

Study population: Patients of or over 18 years old with an acute single shoulder or chest wall injury (rib fracture, disruption of the acromioclavicular (AC) joint Tossy type 1 and 2, not or hardly dislocated fracture of clavicle or proximal humeral bone).

Intervention (if applicable): One group will receive treatment with kinesiotaping, another group receives sham taping (no elastic tape) and the third group receives no taping. This treatment is additional to the general treatment with oral analgesics and a sling (when shoulder injury).

Main study parameters/endpoints: The main study parameter is the proportion of patients who experienced a clinically meaningful reduction in pain score (≥2 points on NRS) at week 1 compared to T1. The kinesiotape group will be compared to the sham group and to the control group.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness:

At 15 minutes after receiving kinesio tape, sham tape or no tape, 1 week, 3 weeks and 8 weeks after visiting the emergency department the pain of these patients is evaluated using NRS by the Brief Pain Inventory (BPI). The effect of use of oral analgesics (questionnaire), on the skin (questionnaire), on independence, activity pattern and progress of pain symptoms (Groningen Activity Restriction Scale (GARS)), comfort and patient satisfaction (Global Perceived Effect (GPE-DV)) is evaluated after 1, 3 and 8 weeks. Physiotherapy is elevated after 8 weeks. Due to the limited seriousness of the injury and the non-invasive nature of the interventions, any serious complication or adverse event is not expected. Benefits of participating this study could be pain reduction in the affected body part.

Inclusion criteria

• ≥18 years
• Acute injury (occurred <24 hours ago)
• Single shoulder or chest wall injury, which includes one of the following injuries:

• rib fracture
• disruption of the AC-joint Tossy type 1 and 2
• not or hardly dislocated fracture of the clavicle
• Not or hardly dislocated fracture of the r proximal humeral fracture

Exclusion criteria

• • Patients younger than 18 years

• Incapacitated persons
• Refusal of participation
• Intubation indication
• Decrease of Consciousness
• Hemodynamic instability
• 3 or more rib fractures
• Rib fracture rib 1-3
• Indication for surgery
• Hospitalization required
• Presence of a haemo- or pneumothorax with chest drain indication
• Already known with allergy for adhesive tape
• Patients with very thin or loose skin on the applicable body part
• Skin infection/irritation or open wound on the applicable body part
• Patients who do not speak Dutch or English