Evaluating music and interaction to reduce patient distress during whole body MRI
Evaluation of a Music and Interaction Intervention on Patient Distress During Whole Body Magnetic Resonance
This study tests if listening to music and having friendly chats with staff can help reduce stress for patients during whole-body MRI scans.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Sex | All |
| Sponsor | European Institute of Oncology Academic / other |
| Locations | 1 site (Milan) |
| Trial ID | NCT06332001 on ClinicalTrials.gov |
What this trial studies
This observational study assesses the impact of a music and interaction intervention on patient distress during whole-body magnetic resonance imaging (WB-MRI). Participants will be randomized into two groups: one receiving the intervention, which includes music of their choice and interaction with trained staff, and a control group receiving standard care. Both groups will complete a distress thermometer and an acceptability questionnaire after the procedure to evaluate their experiences. The study aims to determine if the intervention can improve the acceptability of WB-MRI for patients undergoing this procedure.
Who should consider this trial
Good fit: Ideal candidates are patients scheduled for WB-MRI for detection, staging, therapy monitoring, or screening of malignant neoplasms.
Not a fit: Patients with contraindications to MRI or those undergoing treatment for anxiety disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce patient distress during WB-MRI, improving their overall experience and compliance.
How similar studies have performed: While the specific approach of using music and interaction during WB-MRI is novel, similar interventions in other medical settings have shown positive outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subjects who will undergo to WB-MRI for detection, staging, therapy monitoring or screening. * Acceptance and signature of informed consent. Exclusion Criteria: * Any contra-indication to MRI examination (for example, pacemaker, in the first trimester of pregnancy, metal implants, etc.). * Anxiety disorder and psychological or pharmacological treatments for anxiety
Where this trial is running
Milan
- IEO Istituto Europeo di Oncologia — Milan, Italy (Recruiting)
Study contacts
- Principal investigator: Giuseppe Petralia — European Institute of Oncology
- Study coordinator: Giuseppe Petralia, MD
- Email: giuseppe.petralia@ieo.it
- Phone: +39 02 57489915
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.