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Infant DevelopmentNCT06536296

The Impact of Music Medicine on Preterm Brain Development and Behavior

A study testing Music and Music and parent voice in people with Infant Development and Language Development, run by Brigham and Women's Hospital at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 24 to 30 weeks
What is being tested?
Music and Music and parent voice
Could I receive a placebo?
No, everyone receives an active treatment
How many people
243 participants
Where
2 sitesUnited States
Study dates
19 May 2025to 1 Mar 2031
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 24 to 30 weeks
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • 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

Who cannot join

  • 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.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Carmina Erdei, MD contact

6174620202

cerdei@bwh.harvard.edu

Isabella J Lawandy contact

4014901670

ilawandy@bwh.harvard.edu

United States2 sites, 2 recruiting
  • Brigham and Women's Hospital

    Boston, Massachusetts, 02115

    Elizabeth Singh, MSN, 5125165360, esingh@bwh.harvard.edu

    Recruiting
  • Yale New Haven Hospital

    New Haven, Connecticut, 06510

    Christine Henry, christine.henry@yale.edu

    Angela Montgomery, MD

    Not yet recruiting

Other trials in United States

About this study

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

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.

Read the detailed description

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.

Being tested
Music, Music and parent voice, Standard Care
Keywords
Preterm, Neurodevelopment, Music-based Intervention
Medical subject headings
Premature Birth

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MusicOther

    Also called Arm 1: Music

    Arm 1: Music only

  • Music and parent voiceOther

    Also called Arm 2: Music and parent voice

    Arm 2: Music and parent voice

  • Standard CareOther

    Also called Arm 3: Standard Care

    Standard Care

Study groups in NCT06536296
Study groupRoleWhat they receive
MusicExperimentalWe will create three recordings with increasing complexity for each infant. For each infant developmental stage (32, 34, 36+ weeks PMA), Music Therapists (MTs) in both units will present parents with a curated list of 8-10 musically comparable, familiar lullabies to select from. Songs will be available in different languages reflective of patient diversity, with rhythm, tempo, pitch range/ change, instrumentation, melody, harmony selected drawing on available evidence, including BWH NICU pilot data. Timing: MBI to be administered after regular NICU "care and feeding" times, which are typically considered stressful times for infants. The goal of the intervention will be to provide a calming and relaxing experience to the infant as they "settle" back to sleep after handling times. Music delivery will occur via infant-adapted headphones to facilitate blinding.
Receives: Other: Music
Music and parent voiceExperimentalThe selected lullabies will be pre-recorded by the MT as described above to include a guitar accompaniment track, and a separate vocal track with the MT singing along, in two separate keys to allow variation for parent voice range and comfort. Parents will be invited to sing along with the recorded track of MT singing, and MT will later remove the MT-voice recording track so only the parent voice will be heard with the guitar in the final recording. Timing: MBI to be administered after regular NICU "care and feeding" times, which are typically considered stressful times for infants. The goal of the intervention will be to provide a calming and relaxing experience to the infant as they "settle" back to sleep after handling times. Music delivery will occur via infant-adapted headphones to facilitate blinding.
Receives: Other: Music and parent voice
Reference/ Standard of careActive comparatorThese are infants recruited in the study who will receive the unit standard of care. They will be listening to the NICU ambient noise via infant-adapted headphones but will not receive any music intervention.
Receives: Other: Standard Care

What is being measured

The primary outcome is the main question the study is designed to answer.

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

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

    Measured: 2 years corrected age

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

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

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

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

    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

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

Secondary outcomes (11)
  1. Infant physiology - oxygen saturation

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

    Measured: From enrollment to term-equivalent 37-41 weeks PMA

  2. Infant physiology - respiratory rate

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

    Measured: From enrollment to term-equivalent 37-41 weeks PMA

  3. Infant physiology - heart Rate

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

    Measured: From enrollment to term-equivalent 37-41 weeks PMA

  4. Telomere length

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

    Measured: At enrollment and term-equivalent 37-41 weeks PMA

  5. Neurodevelopmental assessment - cognitive outcomes

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

    Measured: 2 years corrected age

  6. Neurodevelopmental assessment - motor outcomes

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

    Measured: 2 years corrected age

  7. Neurodevelopmental assessment - child behavior outcomes

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

    Measured: 2 years corrected age

  8. Brain development

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

    Measured: Term-equivalent age - 37-41 weeks PMA

  9. Parent stress

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

    Measured: From term-equivalent age to 2 years corrected age

  10. Parent anxiety and depression

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

    Measured: From term-equivalent age to 2 years corrected age

  11. Infant Neurobehavior

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

    Measured: Term-equivalent 37-41 weeks PMA

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Aug 2024
  2. Study start19 May 2025
  3. Primary completion30 Aug 2030 (estimated)
  4. Study completion1 Mar 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
The eligible participants in both institutions will be consecutively approached to enroll in the study. Once informed consent has been obtained, each participant will be randomly assigned to one of the three study groups: M (music), MPV (music with parent voice), or SC (standard care), with 81 infants per each group. We designed the MBI in collaboration with board certified music therapists (MT) at the two institutions. While MBI recordings will be obtained at each NICU timepoint for each infant (with both M and MPV; SC group will wear headphones open to environmental sounds, as a control group), each infant will only listen to one of the three types of recordings according to their group assignment.
Masking
Triple blind
Who is masked
Care provider, Investigator, Outcomes assessor
Enrolment
243 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06536296
Sponsor's protocol ID
2024P001561
Status last verified
Oct 2026
First submitted
10 Jul 2024
Last updated
22 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Music and Music and parent voice in people with Infant Development and Language Development, run by Brigham and Women's Hospital at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 22 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Carmina Erdei, MD (6174620202, cerdei@bwh.harvard.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Bayley-4 language performance (SA3 primary outcome) (time frame: 2 years corrected age). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Oct 2026; AzTrials last refreshed its copy on 26 Oct 2026.

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