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Effect of music therapy on preterm infants

Effect of Classical Music and Lullaby on Physiologic Parameters and Sleep/Awake State of Hospitalized Preterm Infants in NICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012081510606N1
Enrollment
72
Registered
2012-10-08
Start date
2012-03-19
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

physiologic parameters and sleep/awake status. Certain conditions originating in the perinatal period

Interventions

Intervention 1: This study is crossover and every sample is observed one time as control and two anothrt times as intervention groups. every situation lasts for two days. intervention situations incl
This study is crossover and every sample is observed one time as control and two anothrt times as intervention groups. every situation lasts for two days. intervention situations include lullaby and
in classical music situation,0.5 to 1 hr after nutrition we start observation.2 cameras record dependent variables.10 min after start, classical music(Baby Mozzart) is played through 2 speakers, loca
in control situation.every infant is observed 40 min,start 0/5 to 1 hr after nutrition.2 cameras record dependent variables.this situation for every infant includs 2 consecutive days.

Sponsors

Deputy of Research, Faculty of Nursing and Midwifery, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
28 Years to 37 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) infant GA in birth between 27w and 6d and 37w and 0d, 2)no congenital abnormality, no heart or neurologic disease, 3) intact hearing,4)no opiate, sedative or anticonvulsive therapy. Exclusion criteria: 1) all situation causes need for oxygen therapy or respiratory support, 2) increased infant distress or hypersensivity to intervention, 3) discharge, 4) parents refuse to continue.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Respiration rate. Timepoint: every 2 min, for before, simultaneous and after intervention periods. Method of measurement: respiration rate in 1 min,with observation.;Blood pressure. Timepoint: every 5 min for before, simultaneous and after intervention periods. Method of measurement: with osilometric method and bedside monitoring based on mmhg.;Heart rate. Timepoint: every 2 min for before, simultaneous and after intervention periods. Method of measurement: with bedside monitoring.;O2saturation. Timepoint: every 2 min for before, simultaneous and after intervention periods. Method of measurement: based on saturated Hb percentile, with pulseoximeter.;Sleep/awake status. Timepoint: every 2 min for before, simultaneous and after intervention periods. Method of measurement: includ 6 stages based on Brazelton sleep/awake statuses.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPrisa Rafiei

Faculty of Nursing and Midwifery, Tehran University of Medical Sciences

rafie_p@razi.tums.ac.ir+98 21 6693 7120

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026