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Trial to Improve Multisensory Neural Processing, Language & Motor Outcomes in Preterm Infants

Randomized Controlled Trial to Improve Multisensory Neural Processing, Language & Motor Outcomes in Preterm Infants

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03232931
Enrollment
248
Registered
2017-07-28
Start date
2018-10-29
Completion date
2025-04-25
Last updated
2026-03-17

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

Conditions

Preterm Infant

Keywords

auditory, tactile, mother's voice, multisensory

Brief summary

Every year, almost all of ½ million infants born prematurely in the US and 15 million worldwide suffer from abnormal brain maturation resulting from interactions between immaturity and atypical sensory experiences after birth. This study uses rigorous scientific methods to measure the effects and determine the mechanisms of action of a parent-supported multisensory neurorehabilitative intervention for preterm infants, adaptable to a wide variety of neonatal environments, even when parents cannot be at their child's bedside. The intervention aims to improve brain multisensory processing, reactions to sensory stimulation in the home and long term language and motor development.

Detailed description

This study is a randomized controlled trial design with intent-to-treat analysis in hospitalized preterm infants between 32 and 36 weeks post-menstrual age. Both the control and intervention groups will receive routine neonatal intensive care unit care (i.e., skin-to-skin care by parent when available and daily sessions of exposure to recorded parent's voice). In addition to routine care, the parent-supported multisensory intervention consists of sessions of standardized, therapist-administered, auditory-tactile stimulation that combines contingent recorded mother's voice delivered using a pacifier-activated system, during holding with supportive tactile containment against the therapist's chest, covered by cloth imprinted with mother's scent. Possible covariates, multi- and uni-sensory processing, will be measured at entry into the study and immediately after the treatment phase. Event-related potential (ERP) testing will be performed prior to the prior to intervention and after intervention is complete, which occurs at 36 weeks postmenstrual age (PMA) on average. ERP testing will take approximately 30 to 40 minutes. All infants will be seen at the neonatal intensive care unit (NICU) Follow-Up Program clinics at 9-12 months PMA (Year 1) and 22-24 months PMA (Year 2), where neurodevelopmental outcomes will be assessed using standardized methods. Parents will also have the opportunity to consent separately to a secondary part to the study in which their infant would participate in one additional ERP testing session in the NICU between 34-36 weeks PMA and one additional visit to the clinical laboratory for ERP testing between 3-4 months PMA. This optional, secondary part of the study is observational only and does not influence randomization for the main trial. For the secondary part of the study, the population will be 40 of the 230 participants. All parents who are approached for the study prospectively and are randomized to control group will be asked if they would like to participate in the secondary part. Enrollment for this secondary part of the study will stop when 40 participants are reached.

Interventions

BEHAVIORALTherapist skin-to-skin Care

Skin-to-skin (STS) holding is part of the multisensory intervention where the therapist will wear a clean 100% cotton T-shirt with a clean hospital gown on top of the shirt and wrap the "kangaroo" positioner securely over the gown. A gauze square scented with parent's skin will be used to provide olfactory stimulation. Therapist STS sessions occur with simultaneous playing of mother's voice contingent on infant pacifier sucking.

DEVICEContingent parent's voice exposure

The parent's voice recording is delivered via a pacifier-activated music player (PAM). The Pacifier Activated Lullaby® (PAL®) device, is a digital music delivery system that integrates a sensor, a pacifier routinely used in the NICU, and a receiver. It delivers a predetermined 10 seconds of recorded parent's voice singing lullabies upon detection of a suck that meets a preset pressure threshold. The original systems were modified for research use by decreasing the lower limit of activation thresholds for delivering the recording. Minimal effort is required to trigger the device. However, the settings ensure that regular attempts are needed to continue to receive continual presentation of the recording of mother's voice by requiring another suck after 10 seconds. The auditory stimulation with PAL will be provided when the infants are still awake (i.e., at the beginning of the session).

BEHAVIORALParental skin-to-skin care

The standard of care includes parental skin-to-skin care and exposure to parent's voice. During parental skin-to-skin care, infants are placed in a prone position with head positioned over the sternum, allowing transmission of breath and heart sounds to the developing ear. Deeper pressure is applied to offer support and feedback to the child's bottom. Session length is set to a minimum of 45 minutes per unit protocols.

DEVICERecorded parent's voice

Per standard of care, preterm infants in the NICU currently receive noncontingent recorded parents' voice during two 20 minute sessions per day. Recordings are standardized and are played through a sterilizable device (DINO-egg).

Sponsors

Emory University
Lead SponsorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
Nationwide Children's Hospital
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Except for parent reports, all measures will be administered by masked examiners.

Intervention model description

A randomized controlled trial design with intent-to-treat analysis in hospitalized preterm infants between 32 and 36 weeks post-menstrual age. Both the control and intervention groups will receive routine neonatal intensive care protocols (including skin-to-skin care by parent when available and daily sessions of exposure to recorded parent's voice). In addition to routine care, the parent-supported multisensory intervention consists of 10 sessions of standardized, therapist-administered, auditory-tactile stimulation that combines contingent recorded mother's voice delivered using a pacifier-activated system, during holding with supportive tactile containment against the therapist's chest, covered by cloth imprinted with mother's scent. Possible covariates, multi- and uni- sensory processing, will be measured at entry into the study and immediately after the treatment phase. Sensory reactivity will be measured at 1 year and language and motor outcomes will be assessed at 2 years.

Eligibility

Sex/Gender
ALL
Age
32 Weeks to 36 Weeks
Healthy volunteers
No

Inclusion criteria

* Hospitalization at a study location * Postmenstrual age of 32 weeks 0 days gestation to 36 weeks 0 days gestation

Exclusion criteria

* Ventilation using an endotracheal tube * Major congenital malformations * Family history of genetic hearing loss * Use of sedatives or seizure medications Secondary Study Inclusion Criteria: * Enrolled in the control group of the main study

Design outcomes

Primary

MeasureTime frameDescription
Index of Multisensory Processing (IMP)At enrollment up to 36 weeks gestation (prior to intervention), and at intervention completion up to 42 weeks gestationCortical processing is measured as the percentage of time spent in Event Related Potential (ERP) response patterns that have been previously characterized as typical in healthy infants born at full term. ERP is assessed through high-density functional electroencephalogram (EEG) in the NICU. The Index of Multisensory Processing (IMP) is calculated as the percentage of time that the topographical pattern of the participant's ERP to multisensory stimuli is most like template map of a full term infant. The IMP is expressed as a percentage from 100% (samples show nearly-typical activation all of the time) to 0% (samples show nearly-typical activation none of the time).

Secondary

MeasureTime frameDescription
Infant/Toddler Sensory Profile (ITSP) Scoreat 12 months corrected ageThe Infant/Toddler Sensory Profile (ITSP), for ages 7 to 36 months, is a 48-item questionnaire, completed by caregivers, and is used to measure sensory reactivity and adaptation to the environment. The ITSP assesses five sensory processing sections (Auditory, Visual, Tactile, Vestibular, and Oral Sensory Processing) and a General measure. Responses are given on a 5-point scale where 1 = almost always and 5 = almost never. For children 7 to 36 months there are four quadrant scores and one combined quadrant score available. For children 12 months corrected age, the four quadrant score ranges are as follows: Low Registration: 11-55 (typical performance is 46-54) Sensation Seeking: 14-70 (typical performance is 19-35) Sensory Sensitivity: 11-55 (typical performance is 41-52) Sensation Avoiding: 12-60 (typical performance is 45-56) Low Threshold (combined quadrant score): 23-115 (typical performance is 87-107)
Change in Bayley Scales of Infant and Toddler Development - 3rd Edition (Bayley III) Score12 and 24 months corrected ageThe Bayley-III is a standardized comprehensive assessment tool for assessing child development in children one month to 42 months old. The highest possible scaled score on each subtest is 19, and the lowest possible score is 1. Scores from 8 to 12 are considered average. Composite scores for motor and language domains are derived from sums of the subtest scaled scores. Composite scores range from 40-160.
Change in Preschool Language Scales - 5th Edition (PLS-5) Score2 Years (22-26 months corrected age)The PLS-5 is a language assessment tool administered by a trained professional in which children point or verbally respond to pictures or objects. It assesses both receptive (auditory comprehension) and expressive language skills in young children, and a total language score is also calculated. Total scores for Auditory Comprehension, Expressive Communication, and Total Language are standardized with a mean of 100 and a standard deviation of 15. Scores below 100 indicate below average performance while scores above 100 indicate better than average performance.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORNathalie L Maitre, MD, PhD

Emory University

Participant flow

Recruitment details

Participants were recruited from Nationwide Children's Hospital in Columbus, Ohio, and Grady Memorial Hospital and Emory University Hospital Midtown in Atlanta, Georgia, USA. Participant enrollment began October 29, 2018 and data collection for the assessments occurring at up to 42 weeks gestational age was completed by February 20, 2023. The final study assessments were completed by April 25, 2025.

Participants by arm

ArmCount
Multisensory Intervention
Preterm infants in the NICU randomized to receive a multisensory intervention, in addition to the standard of care. The multisensory intervention uses recordings of the parents' voices and nurturing touch administered in the NICU during 12 to 23 sessions of standardized, therapist-administered, auditory-tactile stimulation, dispersed over a 2 to 3 week period. The intervention includes 2 components: (1) holding and light pressure containment of the infant against the hospital-gown covered chest of the therapist for tactile and non-specific auditory stimulation simultaneous with (2) playing of mother's voice contingent on infant pacifier sucking. Additionally, a gauze square scented with parent's skin will be used to provide olfactory stimulation.
112
Standard of Care
Preterm infants in the NICU randomized to receive the standard of care. The standard care for preterm infants in the NICU currently follows medical protocols of skin-to-skin holding and exposure to recordings of parent's voice.
116
Total228

Baseline characteristics

CharacteristicMultisensory InterventionStandard of CareTotal
Age, Continuous34.22 Weeks postmenstrual age (PMA)
STANDARD_DEVIATION 1.22
34.14 Weeks postmenstrual age (PMA)
STANDARD_DEVIATION 1.18
34.18 Weeks postmenstrual age (PMA)
STANDARD_DEVIATION 1.15
Ethnicity (NIH/OMB)
Hispanic or Latino
3 Participants3 Participants6 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
109 Participants113 Participants222 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Gestational age at birth28.84 Weeks postmenstrual age (PMA)
STANDARD_DEVIATION 2.79
28.81 Weeks postmenstrual age (PMA)
STANDARD_DEVIATION 2.91
28.82 Weeks postmenstrual age (PMA)
STANDARD_DEVIATION 2.85
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
3 Participants3 Participants6 Participants
Race (NIH/OMB)
Black or African American
50 Participants56 Participants106 Participants
Race (NIH/OMB)
More than one race
9 Participants1 Participants10 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants1 Participants1 Participants
Race (NIH/OMB)
White
50 Participants55 Participants105 Participants
Region of Enrollment
United States
112 Participants116 Participants228 Participants
Sex: Female, Male
Female
56 Participants61 Participants117 Participants
Sex: Female, Male
Male
56 Participants55 Participants111 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1261 / 122
other
Total, other adverse events
6 / 1261 / 122
serious
Total, serious adverse events
0 / 1261 / 122

Outcome results

Primary

Index of Multisensory Processing (IMP)

Cortical processing is measured as the percentage of time spent in Event Related Potential (ERP) response patterns that have been previously characterized as typical in healthy infants born at full term. ERP is assessed through high-density functional electroencephalogram (EEG) in the NICU. The Index of Multisensory Processing (IMP) is calculated as the percentage of time that the topographical pattern of the participant's ERP to multisensory stimuli is most like template map of a full term infant. The IMP is expressed as a percentage from 100% (samples show nearly-typical activation all of the time) to 0% (samples show nearly-typical activation none of the time).

Time frame: At enrollment up to 36 weeks gestation (prior to intervention), and at intervention completion up to 42 weeks gestation

Population: This analysis includes participants who completed the study and had analyzable event related potential (ERP) data for both study time points. ERP data were not collected for 9 participants in the Multisensory Intervention group and 10 participants in the Standard of Care group. ERP data were collected were not analyzable for 5 participants in the Multisensory Intervention group.

ArmMeasureGroupValue (MEAN)Dispersion
Multisensory InterventionIndex of Multisensory Processing (IMP)Prior to the intervention31.4 percentage of timeStandard Deviation 47
Multisensory InterventionIndex of Multisensory Processing (IMP)After the intervention35.6 percentage of timeStandard Deviation 47
Standard of CareIndex of Multisensory Processing (IMP)Prior to the intervention49.0 percentage of timeStandard Deviation 48
Standard of CareIndex of Multisensory Processing (IMP)After the intervention18.8 percentage of timeStandard Deviation 37
Secondary

Change in Bayley Scales of Infant and Toddler Development - 3rd Edition (Bayley III) Score

The Bayley-III is a standardized comprehensive assessment tool for assessing child development in children one month to 42 months old. The highest possible scaled score on each subtest is 19, and the lowest possible score is 1. Scores from 8 to 12 are considered average. Composite scores for motor and language domains are derived from sums of the subtest scaled scores. Composite scores range from 40-160.

Time frame: 12 and 24 months corrected age

Secondary

Change in Preschool Language Scales - 5th Edition (PLS-5) Score

The PLS-5 is a language assessment tool administered by a trained professional in which children point or verbally respond to pictures or objects. It assesses both receptive (auditory comprehension) and expressive language skills in young children, and a total language score is also calculated. Total scores for Auditory Comprehension, Expressive Communication, and Total Language are standardized with a mean of 100 and a standard deviation of 15. Scores below 100 indicate below average performance while scores above 100 indicate better than average performance.

Time frame: 2 Years (22-26 months corrected age)

Secondary

Infant/Toddler Sensory Profile (ITSP) Score

The Infant/Toddler Sensory Profile (ITSP), for ages 7 to 36 months, is a 48-item questionnaire, completed by caregivers, and is used to measure sensory reactivity and adaptation to the environment. The ITSP assesses five sensory processing sections (Auditory, Visual, Tactile, Vestibular, and Oral Sensory Processing) and a General measure. Responses are given on a 5-point scale where 1 = almost always and 5 = almost never. For children 7 to 36 months there are four quadrant scores and one combined quadrant score available. For children 12 months corrected age, the four quadrant score ranges are as follows: Low Registration: 11-55 (typical performance is 46-54) Sensation Seeking: 14-70 (typical performance is 19-35) Sensory Sensitivity: 11-55 (typical performance is 41-52) Sensation Avoiding: 12-60 (typical performance is 45-56) Low Threshold (combined quadrant score): 23-115 (typical performance is 87-107)

Time frame: at 12 months corrected age

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026