The Effect of Music Therapy as an Adjuvant in the Vital Signs of the Neonate

Neonatal Disease Clinical Trial

Official title:

The Effect of Music Therapy as an Adjuvant in the Vital Signs of the Neonate

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06408064
• Other study ID #: CEIFUS 470-24
• Status: Recruiting
• Phase: N/A
• Start date: May 3, 2024
• Est. completion date: June 30, 2024

Study information

• Verified date: May 2024
• Source: Sanitas University
• Contact: Johana Benavides
• Phone: 57-601-5895377
• Email: jbenavidescr[@]unisanitas.edu.co
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The admission of a newborn to the neonatal intensive care unit (NICU) represents a potentially harmful sound environment coupled with multiple stressful events. However, a strategy such as music therapy (delivered by a trained music therapist) appears to be a non-invasive, safe, and cost-effective alternative that assists newborns in their physiological self-regulation with a beneficial effect on stabilizing neonatal vital signs, so it can be used as a complementary strategy to medical management. The aim of this study is to determine the effect of live and pre-recorded music therapy on vital sign variables in newborns older than 32 weeks hospitalized in the neonatal intensive care unit of a high-complexity health institution in Colombia.

Description:

A parallel, controlled randomized clinical trial will be conducted.

Study Population: Newborns older than 32 weeks gestational age at birth hospitalized in the Neonatal Intensive Care Unit of a high-complexity health institution who meet the inclusion criteria.

Outcomes: Heart rate will be primary outcome. Respiratory rate and oxygen saturation will be secondary outcomes. The patient monitor will be utilized to measure the heart rate, respiratory rate, and oxygen saturation.

Standardization of measurements:

First, the trademarks of the medical equipment manufacturers of each of the tools that will be used (vital sign monitor and pulse oximeter) will be verified to ensure that they correspond to the same commercial brand. Since different brands may exhibit variability in standard calibration measurements within the critical range, it is important to verify that the tools are of the same brand. Secondly, it will be verified that each medical tool used has been calibrated within the previous six months, with the date of the last calibration recorded so that the device can be used during the study. Subsequently, the professional in charge of the music company will verify that the guitar to be used during the live music is in tune and suitable for use. A decibel regulator will be employed during the implementation of both pre-recorded and live music, adjusting the volume of the emitted sound. This will ensure that the decibels emitted by each research subject remain within the permitted range of 70 decibel (dB). Vital variables will be recorded at minute 0, from minute 0 to minute 10 continuously, and at 30 minutes after the intervention.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 45
• Est. completion date: June 30, 2024
• Est. primary completion date: June 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 32 Weeks to 40 Weeks

Eligibility

Inclusion Criteria:

• Newborns with gestational age at birth greater than or equal to 32 weeks.

• Birth weight greater than or equal to 1500 grams.

• Be at least 72 hours of postnatal age.

Exclusion Criteria:

• Respiratory disturbances in the last 48 hours such as: Apnea or Brief Resolved Unexplained Events (BRUE), need for invasive mechanical ventilation

• Hemodynamic alterations in the last 48 hours such as: Hypotension (systolic, diastolic, or mean BP < P5) or hypertension (systolic, diastolic, or mean BP > P95), bradycardia (HR < 100/min), shock of any etiology, requirement for volume expanders, infusion of inotropics, vasodilators and/or prostaglandin E1.

• Neurological alterations such as: Perinatal asphyxia at birth manifested by the need for resuscitation, APGAR < 3 at 5 minutes and/or = 5 at 10 minutes, and metabolic acidosis in cord gases with a potential of hydrogen (pH) < 7 and base excess (BE) < -12, hypoxic-ischemic encephalopathy, seizure syndrome for up to 48 hours after the last clinical event or alteration of the brain pattern, interventricular hemorrhage in preterm infants in the first week of diagnosis.

• Management with Extracorporeal membrane oxygenation (ECMO) and/or nitric oxide

• Temperature less than 36.5 C or greater than 37.5 C.

• Patient under pharmacological sedation or use of beta-blockers.

• Congenital heart disease, operated on or not.

• Congenital malformations

• Surgical emergencies or recovery from a surgical procedure performed within the last 48 hours.

Related Conditions & MeSH terms

• Infant, Newborn, Diseases
• Neonatal Disease

Intervention

Other:
• Music therapy
Music therapy is a non-pharmacological therapeutic intervention that will be implemented through two modalities: live and pre-recorded instrumental lullabies music.The volume control will be conducted within the groups through the use of a decibel regulator, with a maximum volume of 70 dB. During the intervention and for a period of 30 minutes following its conclusion, singing will be prohibited by the music therapist or the parents. Both live and pre-recorded music will be instrumental in nature, lacking any lyrics.

Locations

Country	Name	City	State
Colombia	Clínica Universitaria Colombia	Bogotá

Sponsors (2)

Lead Sponsor	Collaborator
Claudia Aristizábal	Sanitas University

Country where clinical trial is conducted

Colombia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Heart rate	The measurement will be continuously quantified in terms of number of pulsations per minute continuously.	The baseline measurement will be taken before the intervention, and will continue for 30 minutes during the intervention and for a further 30 minutes after the intervention has been completed.
Secondary	Respiratory rate	The measurement will be continuously quantified in terms of the number of breaths per minute.	The baseline measurement will be taken before the intervention, and will continue for 30 minutes during the intervention and for a further 30 minutes after the intervention has been completed.
Secondary	Oxygen saturation	The measurement will be continuously quantified in terms of proportion per minute.	The baseline measurement will be taken before the intervention, and will continue for 30 minutes during the intervention and for a further 30 minutes after the intervention has been completed.