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.
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
- Conditions the study is for
- Infant Development, Language Development, Prematurity
- 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.
United States2 sites, 2 recruiting
- Recruiting
Brigham and Women's Hospital
Boston, Massachusetts, 02115
Elizabeth Singh, MSN, 5125165360, esingh@bwh.harvard.edu
- Not yet recruiting
Yale New Haven Hospital
New Haven, Connecticut, 06510
Christine Henry, christine.henry@yale.edu
Angela Montgomery, MD
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.
- Conditions
- Infant Development, Language Development, Prematurity, Stress
- 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 group | Role | What they receive |
|---|---|---|
| Music | Experimental | We 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 voice | Experimental | The 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 care | Active comparator | These 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.
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
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)
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)
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
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
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
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
Neurodevelopmental assessment - cognitive outcomes
Study patients' cognitive performance measured on the Bayley-4 assessment at 2 years corrected age
Measured: 2 years corrected age
Neurodevelopmental assessment - motor outcomes
Study patients' motor performance measured on the Bayley-4 assessment at 2 years corrected age
Measured: 2 years corrected age
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
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
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
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
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.
- First posted2 Aug 2024
- Study start19 May 2025
- Primary completion30 Aug 2030 (estimated)
- Study completion1 Mar 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Infant DevelopmentStudies of the same condition, open and under way.
- More trials run by Brigham and Women's HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Brigham and Women's Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Yale New Haven Health System Center for Healthcare Solutions
- Responsible party
- Principal investigator, Carmina Erdei, MD, Brigham and Women's Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 22 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Impact of Music Medicine on Preterm Brain Development and Behavior - A Two-Center Randomized Controlled Trial "The Lullaby Study"
- ClinicalTrials.gov ID
- NCT06536296
- Acronym / sponsor ID
- 2024P001561
- Conditions
- Infant Development, Language Development, Prematurity, Stress
- Keywords
- Preterm, Neurodevelopment, Music-based Intervention
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 243 participants (estimated)
- Lead sponsor
- Brigham and Women's HospitalUniversity, hospital or other
- Collaborators
- Yale New Haven Health System Center for Healthcare Solutions
- Study start
- 19 May 2025 (actual)
- Primary completion
- 30 Aug 2030 (estimated)
- Study completion
- 1 Mar 2031 (estimated)
- First posted
- 2 Aug 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (care provider, investigator, outcomes assessor)
- Number of arms
- 3
- 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.
| Arm | Type | Receives |
|---|---|---|
| Music | Experimental | Other: MusicWe 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. |
| Music and parent voice | Experimental | Other: Music and parent voiceThe 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. |
| Reference/ Standard of care | Active comparator | Other: Standard CareThese 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. |
Who may qualify
- Ages
- 24 to 30 weeks
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (2 listed)
- 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
Key exclusion criteria (4 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MusicAlso: Arm 1: MusicArm 1: Music only | Other | Music |
| Music and parent voiceAlso: Arm 2: Music and parent voiceArm 2: Music and parent voice | Other | Music and parent voice |
| Standard CareAlso: Arm 3: Standard CareStandard Care | Other | Reference/ Standard of care |
Primary outcome
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
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
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
11 secondary outcomes
Infant physiology - oxygen saturation
Time frame: From enrollment to term-equivalent 37-41 weeks PMA
Infant physiology - respiratory rate
Time frame: From enrollment to term-equivalent 37-41 weeks PMA
Infant physiology - heart Rate
Time frame: From enrollment to term-equivalent 37-41 weeks PMA
Telomere length
Time frame: At enrollment and term-equivalent 37-41 weeks PMA
Neurodevelopmental assessment - cognitive outcomes
Time frame: 2 years corrected age
Neurodevelopmental assessment - motor outcomes
Time frame: 2 years corrected age
Neurodevelopmental assessment - child behavior outcomes
Time frame: 2 years corrected age
Brain development
Time frame: Term-equivalent age - 37-41 weeks PMA
Parent stress
Time frame: From term-equivalent age to 2 years corrected age
Parent anxiety and depression
Time frame: From term-equivalent age to 2 years corrected age
Infant Neurobehavior
Time frame: Term-equivalent 37-41 weeks PMA
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Oct 2026.
- Individual participant dataSharing planned: Undecided
Related trials for Infant Development
Recruiting
Nutritional Maturity in Preterm Newborns (Premature Infant Oral Motor Intervention, PIOMI)
Preterm, Preterm Infant Development
Active, not recruiting
Mother and Infant Home Visiting Program Evaluation
Pregnancy, Infant Development
Active, not recruiting
Investigating Baby Behavior and Family Technology Use Study
Mobile Phone Use, Mother-Infant Interaction
Not yet recruiting
Effect of a Telerehabilitation-Supported, Family-Centered Early Intervention Program on Neurodevelopmental and Parental Outcomes in Infants at Mild-to-Moderate Risk
Development Delay, Motor Skills Disorders
Recruiting
Methyl Donor-Rich Diet in the Postpartum Period
Postpartum Depression (PPD), Breastfeeding
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 1 country: see every site and its status.
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.