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NCT Number: NCT06536296

The Impact of Music Medicine on Preterm Brain Development and Behavior

The investigators are conducting a two-site randomized control trial with the aim of defining the impact of music (M) without or with parent voice (MPV) on very preterm infants' acute and cumulative stress, intranetwork connectivity on term brain MRI, and language and other neurodevelopmental outcomes at two years corrected age. This is based on the hypothesis that infants in MPV arm are expected to experience the greatest benefit compared with infants receiving standard care.

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Key information

Age range

24 week–30 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yale New Haven Hospital, New Haven, Connecticut, United States

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About this study

Preterm birth remains the leading cause of death for children under five. For survivors, it also accounts for high morbidity and substantial physical, psychosocial, emotional, and financial burden for individuals, families, and communities. The impairments span over multiple domains, with language difficulties affecting about half of surviving children. Evidence indicates that preterm birth has significant impacts on long-term functioning, yet primary prevention of preterm birth is presently not feasible. It is therefore imperative to prioritize early interventions to mitigate these adverse long-term effects on child and family outcomes.

Very preterm (VP) infants, i.e., those born below 32 weeks gestational age (GA) typically spend 2-4 months hospitalized in the Neonatal Intensive Care Unit (NICU) before reaching term-equivalent age (TEA). During this time, the preterm brain nearly quadruples in volume and is highly sensitive to both positive and negative environmental experiences. Yet, during this period, VP infants must also receive life-saving intensive medical care in the sensory-atypical environment of the NICU. From an auditory perspective, this atypical environment comprises loud equipment sounds at volumes far exceeding recommended levels, silence, and a paucity of human interaction. One domain of neurosensory experience is the auditory environment, comprised predominantly of non-meaningful, high-frequency/ high decibel equipment sounds, and silence. The deprivation of VP infants from enriching auditory experiences (parental voice, infant-directed language) combined with the constant influx of high frequency/high decibel sounds (alarms and electronic noise) can induce chronic stress and negatively impact auditory and other areas of cortical development.

For preterm infants who have not yet reached term-equivalent age (TEA), the NICU hospitalization is a critical window for developmental adaptability to experience during a highly sensitive period of brain development. There are two key pathways whereby music and voice therapy in the VP infant are thought to have benefit - stress reduction and auditory enrichment. Recent work indicates that music therapy may reduce the immediate stress experienced by VP infants, with evidence emerging on its impact to improve neurodevelopmental outcomes. Prior studies have been limited due to small size, variability of music exposures, inconsistent study design and outcome measures. Further, most studies explored exposure-outcome associations, without mechanistic investigation. One study showed improved white matter maturation in acoustic radiations, larger amygdala volumes, and enhanced functional connectivity brain magnetic resonance imaging (MRI) after early music exposures. These suggests that early music exposure may enhance auditory cortex development and reduce stress (amygdala) in VP infants.

While small studies inform these hypotheses, a large, randomized trial is necessary to test them more rigorously. Our own center's pilot study demonstrated that a music condition with low, repetitive, and rhythmically consistent entrainment stimulus was associated with improved physiologic state after the exposure. Based on these data, the investigators plan to further develop an individualized intervention encompassing evidence-based musical elements onto which parental voice will be carefully layered. The aim of this proposal is to conduct a randomized trial to determine the effects of a protocolized music-based intervention (MBI) with and without parental voice on stress reduction, early brain structure and function, and neurodevelopmental outcomes.

The investigators propose to address this knowledge gap in a large, two-center randomized controlled trial (RCT), employing a novel MBI tailored based on available preliminary data and inclusive of musical and non-musical elements to facilitate parent engagement, with comprehensive evaluation of relevant clinical, neuroimaging, and neurodevelopmental outcomes of VP infants up to two years of age. The impact of this work will be two-fold: this proposal will 1) generate rigorous evidence to specifically support the integration of music medicine as a therapeutic approach for VP infants in the NICU, and 2) strengthen the evidence base for neurosensory interventions for hospitalized infants, which will shift the framework of care in the NICU by leveraging developmental care interventions to optimize the outcomes of VP infants.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Very preterm infants born between 24+0 and 30+6 weeks' gestational age (GA) from 2 level III NICUs (Brigham and Women's Hospital, Boston, MA and Yale New Haven, CT)
  • Infants who are medically stable per the clinical care team

Exclusion criteria

  • Infants with major genetic or congenital anomalies known to be associated with developmental delay
  • Infants with severe brain injury (such as intraparenchymal hemorrhage, severe white matter injury)
  • Infants who are severely ill infants for whom MBI is not feasible
  • Infants of parents who cannot complete questionnaires in English or Spanish.

Treatment and study plan

Music

Other

Arm 1: Music only

Other names: Arm 1: Music

Music and parent voice

Other

Arm 2: Music and parent voice

Other names: Arm 2: Music and parent voice

Standard care

Other

Standard Care

Other names: Arm 3: Standard Care

Primary outcomes

  1. Bayley-4 language performance (SA3 primary outcome)

    Time frame: 2 years corrected age

    Study patients Language performance measured on the Bayley-4 at 2 years corrected age

  2. Amygdala volume on MRI (SA1a, primary outcome)

    Time frame: At term-equivalent (~ 3 months of age), 37-41 weeks postmenstrual age (PMA)

    Amygdala volume as a proxy of cumulative stress measured on term-equivalent brain MRI

  3. Intranetwork connectivity in Salience and Language networks (SA2a, primary outcome)

    Time frame: Term-equivalent (~ 3 months of age), 37-41 weeks postmenstrual age (PMA)

    We will measure the intranetwork connectivity in Salience and Language networks in infants exposed to music and music with parent voice compared those in SC arm at term-equivalent

Secondary outcomes

  1. Infant physiology - oxygen saturation

    Time frame: From enrollment to term-equivalent 37-41 weeks PMA

    We will record infant physiologic vital signs (i.e. oxygen saturation) from infants' bedside monitor around each study intervention

  2. Infant physiology - respiratory rate

    Time frame: From enrollment to term-equivalent 37-41 weeks PMA

    We will record infant physiologic vital signs (i.e. respiratory rate) from infants' bedside monitor around each study intervention

  3. Infant physiology - heart Rate

    Time frame: From enrollment to term-equivalent 37-41 weeks PMA

    We will record infant physiologic vital signs (i.e. heart rate) from infants' bedside monitor around each study intervention

  4. Telomere length

    Time frame: At enrollment and term-equivalent 37-41 weeks PMA

    Assess infant premature aging at term-equivalent by measurement of telomere length on blood samples

  5. Neurodevelopmental assessment - cognitive outcomes

    Time frame: 2 years corrected age

    Study patients' cognitive performance measured on the Bayley-4 assessment at 2 years corrected age

  6. Neurodevelopmental assessment - motor outcomes

    Time frame: 2 years corrected age

    Study patients' motor performance measured on the Bayley-4 assessment at 2 years corrected age

  7. Neurodevelopmental assessment - child behavior outcomes

    Time frame: 2 years corrected age

    Study patients' behavioral performance measured on the Child Behavior Checklist at 2 years corrected age

  8. Brain development

    Time frame: Term-equivalent age - 37-41 weeks PMA

    Brain development and injury classified using the established Kidokoro scoring system applied to term-equivalent brain MRI

  9. Parent stress

    Time frame: From term-equivalent age to 2 years corrected age

    Assessment of parent stress (Parental Stressor Scale) using a standardized survey of families of study infants

  10. Parent anxiety and depression

    Time frame: From term-equivalent age to 2 years corrected age

    Assessment of parent anxiety and depression (Hospital Anxiety and Depression Scale) using one standardized survey that provides a combined score

  11. Infant Neurobehavior

    Time frame: Term-equivalent 37-41 weeks PMA

    We will assess infant neurobehavior using the Hammersmith Neonatal Neurological Examination at term-equivalent age 37-41 weeks PMA

Study contacts

Contact information is provided by the study sponsor or research team.

Carmina Erdei, MD

CONTACT

[email protected]

6174620202

Isabella J Lawandy

CONTACT

[email protected]

4014901670

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Collaborators

  • Yale New Haven Health System Center for Healthcare Solutions

Registry information

Official study title

The Impact of Music Medicine on Preterm Brain Development and Behavior - A Two-Center Randomized Controlled Trial "The Lullaby Study"

Important dates

Study start
2025
Primary completion
2030
Study completion
2031
First posted
Aug 2, 2024
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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