Effects of Music on Preoperative Anxiety in Patients With Femoral Fractures Undergoing Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAzienda Unita Sanitaria Locale di Piacenza

About this trial

This randomized controlled trial (RCT) investigates the effectiveness of music therapy in reducing preoperative anxiety among elderly patients with femoral fractures. Preoperative anxiety is known to worsen physiological stability, increase pain perception, and negatively impact recovery, yet specific evidence on non-pharmacological interventions like music therapy in the orthogeriatric setting is lacking.

The study will enroll 154 adult patients admitted to the Orthogeriatrics Unit for elective femoral fracture surgery. Participants will be randomly assigned to receive either a 20-minute session of music therapy or standard care. Anxiety will be measured using the APAIS scale, and pain will be assessed with the NRS scale, both before and after the intervention.

The trial is designed as a blinded, prospective RCT, with data collected and managed under current privacy regulations. By generating robust data on this low-cost, safe intervention, the study aims to improve preoperative management and patient outcomes in orthopedic surgical care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients of both sexes, 18 years of age or older

Patients with femur fracture who are candidates for surgery

Able to provide informed consent.

Disqualifiers

Patients with a diagnosis of hearing loss

Patients diagnosed with cognitive or psychiatric disorders

Patients undergoing emergency/emergency surgery

Trial design

Design model

Parallel

Treatments tested in this trial

  • Music intervention

    Other intervention

    patient enrolment, administration of the APAIS and NRS scales (T0), administration of the standard music therapy/assistance intervention (20 minutes duration), re-evaluation with re-administration of the APAIS and NRS scales (T1) and completion of the CRF. The administration will take place at the patient's bedside, respecting the privacy and confidentiality of the subjects involved, guaranteeing absolute tranquillity, also with the help of dividers to avoid distractions and interruptions.

Treatment groups

154 Participants
are divided into 2 treatment groups
Group A: MUSIC THERAPYExperimental treatment 1 intervention
Group B: NO MUSICTHERAPYNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Difference between the Amsterdam Preoperative Anxiety and Information Scale (APAIS) at T0 and T1

Difference in preoperative anxiety level after 20 minutes and baseline evaluated by APAIS scores between T0 and T1. The APAIS consists of six questions, with each question rated on a 5-point Likert scale (1=not at all, 5=extremely), and has a minimum score of 6 and a maximum score of 30. Higher APAIS scores indicate a worse outcome with higher levels of anxiety and a greater desire for information.

Time frame
Baseline and 20 minutes after baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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