About this trial
Fractures of the distal end of the radius are one of the most frequent fractures diagnosed in the emergency room. The initial management, and in many cases definitive, is carried out through manipulation, closed reduction and immobilization in the emergency room. Different methods of anesthesia have been described to reduce pain during the manipulation and reduction procedure, such as: hematoma block, periosteal block, general anesthesia, intravenous regional anesthesia, nitrous oxide, intramuscular sedation, and conscious sedation. Despite the use of different methods of anesthesia, none is fully effective and each of these methods is not free of complications. Adjuvant measures could play an important role in improving the patient's experience during the procedure, however, there is little evidence in this regard.
Music is increasingly being studied and developed as an adjunctive therapy in the management of pain and anxiety in different medical procedures, demonstrating a statistically significant reduction in pain and anxiety. However, in the literature there is no evidence of studies that evaluate the effect of music during the reduction of fractures in traumatology as an adjuvant therapy for the management of pain and anxiety.
In our experience, despite the anesthesia used, reductions of distal radius fractures are usually a painful procedure that involves a certain degree of discomfort for the patient. For this reason, the investigators believe this study is necessary, as it could demonstrate a new adjuvant therapy that reduces pain and anxiety and improves the overall experience of the patient, in addition to being music, a low-cost tool with no risks for patient safety.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients older than 18 years.
Clinical and radiological diagnosis of a fracture of the distal end of a closed radius that has an indication for closed reduction.
Disqualifiers
Diagnosis of other concomitant fractures.
Allergy to local anesthetics.
Significant hearing impairment and/or use of hearing aids.
Patients whose comorbidities prevent correct participation in the procedure (such as cognitive impairment, diagnosis of psychiatric diseases, patients under the influence of drugs...).
Trial design
Parallel
Treatments tested in this trial
No Music
DeviceNo listening to music while intervention is carried out
Music
DeviceListening to music while intervention is carried out
Treatment groups
Trial outcomes
Primary outcomes
Change in VAS scale for pain
It will be completed after the procedure and the punctuation will go from 0 to 10
Change in Anxiety STAI-6
Puntuation between 20 and 80, 50 considered high anxiety level
Secondary outcomes
Cardiac frequency
Measurement of the cardiac frequency assessed before, during and after fracture immobilization
Blood pressure
Measurement of the blood pressure will be assessed before, during and after fracture immobilization
Satisfaction after procedure
1 to 5 scale for satisfaction with the procedure
Sponsors and contacts
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