Infant Development

33

Review clinical trials related to Infant Development. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Breastmilk in Response to a Bout of Exercise

The purpose of this study is to unveil the mechanistic benefits of a bout of postpartum maternal exercise on infant health that are provided by breastmilk.

Participants needed: 60
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Mayo ClinicUpdated: Jun 24, 2026Locations: 1Duration: 1 Month
Eligibility criteria

Active coronary artery disease or heart failure. [+12]

Status: Recruiting

Developmental Impacts of Microplastics Exposure in Early Life

The goal of this observational study is to characterize and evaluate micro- and nano-plastic (MNP) exposures among mothers and infants in mother-infant dyads 1 or 3 months postpartum living in Baltimore, Maryland. The main questions it aims to answer are: * What MNPs are present in breastmilk and maternal blood samples and in their infants stool sample? * Are there associations between amount of maternal MNPs in breast milk and mass of MNP particles in infant stool? * Which environmental and lifestyle factors are most predictive of maternal MNP burden? * Is infant exposure to MNPs associated with birth weight and postnatal growth trajectories? Participants will: * Complete several questionnaires assessing medical histories, lifestyle factors, environmental exposures, eating behaviors, etc. * Provide biological specimens including: maternal blood, stool, and breastmilk; infant stool * Clinical visit to have anthropometric measures documented including maternal height and weight, infant weight, length, and skin-fold thickness

Participants needed: 40
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Johns Hopkins Bloomberg School of Public HealthUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

All gender expressions [+4]

Physical, mental, or cognitive disability that prevents participation; current i... [+7]

Status: Recruiting

Screening for Autism in 9-Month-Olds by Measuring Social Visual Engagement

The goal of this project is to measure the clinical utility of an objective and quantitative eye-tracking assay collected on a standalone, mobile investigational device to accurately screen 9-month-old infants for autism spectrum disorder and other actionable delays.

Participants needed: 2,120
Trial details
Age: 8-10Biological sex: AllType: ObservationalSponsor: Emory UniversityUpdated: Jun 4, 2026Locations: 2
Eligibility criteria

Infants between the chronological ages of 8-10 months [+2]

Status: Recruiting

The Playful Learning in Infancy Program

In the Playful Learning in Infancy Program, parents receive research-based educational guidance on playful interactions with their infants aged 0-1 year. They learn to recognize their infants' cues indicating readiness to engage in play and they are introduced to specific, developmentally appropriate activities for interactive engagement. The guidance is delivered to parents during routine home visits by public health visitors. The aims of the Playful Learning in Infancy Program are to 1) promote playful interactions between infants and parents, parental attitudes towards play, and infant socioemotional development; 2) enhance the language and knowledge of playful learning in infancy among frontline staff; and 3) evaluate the Playful Learning in Infancy Program for potential testing in a future large-scale RCT study. Evaluation is based on a parallel group study design, with half of the participants receiving care as usual and half of the participants receiving care as usual along with the Playful Learning in Infancy Program.

Participants needed: 2,327
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of CopenhagenUpdated: May 26, 2026Locations: 1
Eligibility criteria

Residence address in the Danish municipalities of Hvidovre or Billund [+3]

Parental age under the age of 18 when the child is born [+1]

Status: Not yet recruiting

Breastfeeding Education Support Tool

The proposed project seeks to evaluate the effectiveness and implementation of the Breastfeeding Education Support Tool for Baby (BEST4Baby) intervention, an mHealth-supported community-based peer counselor breastfeeding intervention for mothers in India. Given that rates of optimal infant feeding practices have remained stagnant over the past two decades in India, and that India is the most populous country and icontributes one-fifth of all global live births, this project could have major global health implications if the intervention is found to improve maternal breastfeeding practices and infant clinical outcomes. The project will also provide evidence needed to adopt BEST4Baby nationally and in other low resource communities.

Participants needed: 336
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Thomas Jefferson UniversityUpdated: May 5, 2026Locations: 1
Eligibility criteria

at least 18 years of age, [+7]

Status: Recruiting

Cortical Tracking of Speech in the First Year of Life

The goal of this observational study is to investigate early neural mechanisms underlying the processing of spoken language, specifically the phenomenon of cortical tracking, and to determine whether these mechanisms can serve as early predictors of later language development outcomes in infants, including both typical and atypical trajectories. The main questions it aims to answer are: * How do infants with and without a familial history of language and learning impairments differ in their neural ability to track speech and non-speech auditory stimuli at an early stage of development (around 8 months of age)? * To what extent do early cortical tracking mechanisms predict later language abilities, including both receptive and expressive skills, measured at approximately 18 months of age? Researchers will compare infants with a familial risk for language and learning impairments (FH+) to infants without such risk (FH-) to determine whether differences in early neural processing of auditory stimuli are associated with later language outcomes. Participants will: * undergo a neurophysiological assessment involving non-invasive electroencephalographic (EEG) recording while being exposed to auditory stimuli, including: speech stimuli (pre-recorded simple stories in Italian, presented in infant-directed speech); non-speech stimuli (musical sounds matched for rhythmic and acoustic properties) * take part in a developmental assessment at approximately 8 months of age, including standardized measures of cognitive and early linguistic abilities * be involved in a follow-up assessment approximately 10 months later (around 18 months of age), during which standardized tests will evaluate language comprehension and production abilities * have additional background information collected, including family history of language and learning disorders and socio-demographic characteristics, to better understand potential risk and protective factors The study follows a longitudinal design and uses non-invasive procedures that do not require active responses from the infant.

Participants needed: 50
Trial details
Age: 30-34Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Apr 15, 2026Locations: 1
Eligibility criteria

Healthy infants aged between 7 and 8 months [+2]

Gestational age < 37 weeks and/or birth-weight < 2500 grams [+3]

Status: Recruiting

Mediterranean Diet on Pregnancy and Foetus Development

The Mediterranean-style diet has been associated with longevity, long-life wellbeing, lower risk of cardiovascular disease, cancer, obesity, and metabolic syndrome. Research is pointing to the benefits that MeD could have in pregnant. Pregnancy is a very complex period and recently, the attention has been focused on the possibility that healthy dietary patterns positively influence pregnancy and the development of organs in the offspring. The mechanisms through which MeD influences pregnancy and fetal growth may partly depend on its antinflammatory properties and possibly on changes in epigenetic mechanisms. Systemic inflammation might contribute to the association between maternal obesity and less favorable neurodevelopmental outcomes. The investigators aim to define how maternal adhesion to MeD may affect pregnancy and new-born development, hence representing a notable burden from a public health and social perspective. Main objective of this project is to build up a birth cohort suitable to investigate the role of maternal dietary habits on maternal and new-born health, with special focus on MeD and its possible mechanism of action through epigenetic and inflammation changes. To establish a mother/new-born cohort, collect detailed information on maternal dietary habits and set-up a biobank of biological samples to evaluate the association between dietary habits and pregnancy outcomes. The investigators will recruit 2000 pairs (mother, new-born) in different obstetrics departments. To investigate the association between maternal dietary habits, foetal growth and offspring development and possible mediation by the inflammation profile of the mother. To understand whether maternal dietary habits are associated with epigenetic changes in the offspring and if this process is driven by the inflammation profile of the mother. Venous blood samples will be obtained at the baseline and at each gestational period for ultrasound at 11-13 gestational weeks, 20-22 weeks and 30-32 weeks. Women will be followed-up with standard clinical and 2D ultrasound examinations at gestational weeks 11-13, 20-22 and 30-32 to evaluate the fetal growth. Offspring development will be assessed at 6, 12, 18, 24 months of age. After delivery, the investigators will collect umbilical cord blood and saliva samples from new-born using standard procedures. To understand if new-born epigenetics is associated with infant physical and neurocognitive development in the following 2 years.

Participants needed: 2,000
Trial details
Age: 18-50Biological sex: FemaleType: ObservationalSponsor: Neuromed IRCCSUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

pregnant women attending the Units of Obstetrics and Gynecology at Neuromed Clin... [+2]

pregnancy with foetuses with known chromosomal or congenital malformation [+6]

Status: Recruiting

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.

Participants needed: 243
Trial details
Age: 24-30Biological sex: AllType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Mar 25, 2026Locations: 2
Eligibility criteria

Very preterm infants born between 24+0 and 30+6 weeks' gestational age (GA) from... [+1]

Infants with major genetic or congenital anomalies known to be associated with d... [+3]

Status: Recruiting

Measurement of Energy Metabolism in Infants

The purpose of this study is to measure energy expenditure during the first 3 months of life in infants.

Participants needed: 70
Trial details
Age: 1-3Biological sex: AllType: ObservationalSponsor: Pennington Biomedical Research CenterUpdated: Mar 18, 2026Locations: 1
Eligibility criteria

Healthy, full-term infant [+3]

Unable to complete 3 clinic visits within about 14 days at Pennington Biomedical... [+5]

Status: Recruiting

Understanding Early Development of Infants and Toddlers

The goal of this observational study is to analyze early development in infants and young children from a biopsychosocial perspective, with a particular focus on cognitive, language, motor, social-emotional, and adaptive functioning during the first years of life. The study will include infants and young children from 16 days of age up to 42 months of age, assessed during a single diagnostic session conducted by qualified specialists. The developmental assessment will include standardized diagnostic tasks and direct observation of behavior in the form of play and natural interaction, carried out in the presence of a parent or legal guardian. In addition, information regarding the child's everyday functioning will be collected from parents or caregivers using standardized questionnaires, including data on social-emotional competencies, communication, and adaptive skills. The main research questions addressed by this study are: What is the developmental profile of infants and young children in the first years of life? What relationships exist between different domains of early development within a biopsychosocial model of child functioning? Can specific developmental patterns be identified that indicate an increased risk of developmental difficulties in early childhood? How does age differentiate the structure and variability of developmental functioning across assessed domains? The study is non-invasive and observational in nature. Data will be analyzed exclusively in aggregated form and will contribute to a better understanding of early child development as well as to the development of norms and tools supporting early diagnosis and developmental intervention.

Participants needed: 1,200
Trial details
Age: 16-42Biological sex: AllType: ObservationalSponsor: Bartosz M. RadtkeUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

Infants and young children aged from 16 days to 42 months at the time of assessm... [+3]

Severe acute medical condition at the time of assessment preventing participatio... [+4]

Status: Recruiting

Continuous Delivery Room Skin-to-skin-study for Moderate and Late Preterm Infants

The goal of this randomized controlled trial is to compare the effect of direct skin-to-skin contact in moderate and late preterm infants. The main questions it aims to answer are: * does skin-to-skin contact in moderate and late preterm infants influence gene expression in the stress signaling pathway? * does skin-to-skin contact in moderate and late preterm infants improve the short- and long-term outcome? Participants will either get immediate separation after vaginal birth or receive immediate skin-to-skin contact. Researchers will compare these two groups to answer the proposed questions.

Participants needed: 60
Trial details
Biological sex: AllType: InterventionalSponsor: University of CologneUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

preterm birth between gestational age of 32 0/7 and 36 6/7 weeks [+3]

malformations or syndromes of the infant [+3]

Status: Recruiting

Neuroimaging of Babies During Natural Sleep to Assess Typical Development and Cerebral Palsy

Background: Early diagnosis of cerebral palsy (CP) is crucial, enabling intervention when neuroplasticity is at its highest. Magnetic resonance imaging (MRI) plays a vital role in CP diagnosis. Currently, diagnostic MRI of newborns and infants with suspected brain damage relies heavily on structural MR images. The current study aims to i) establish procedures for clinical infant and toddler MRI during natural sleep, ii) use advanced MRI sequences, such as advanced diffusion-weighted imaging (DWI), that may be more sensitive in detecting early brain damage, and iii) map relationships between early brain development, and motor function and development. Methods: The NIBS-CP study will enroll approximately 200 infants either at risk for CP or typically developing. Infants will be followed longitudinally (for three waves) between 3 months and 2 years of age with cerebral MRI at 3 Tesla and comprehensive assessments of motor and cognitive functioning. The MRI protocol includes advanced diffusion-weighted imaging, high-resolution structural MRI, and MR spectroscopy. The motor and cognitive assessments include Hand Assessment in Infants, Alberta Infant Motor Scales, Hammersmith Infant Neurological Examination, Peabody Developmental Motor Scales, Bayley Scales of Infant Development, and Ages and Stages Questionnaires. NIBS-CP aims to establish normative material on early brain development of Danish children and conduct normative modeling of typical and atypical development to identify deviations in brain development at the level of the single child. Discussion: Identifying predictive brain structural features of motor function and motor development is key to the future use of early MRI in the clinical work-up, as this promotes early diagnosis and (clinical) intervention strategies tailored to the individual child.

Participants needed: 200
Trial details
Age: 2-11Biological sex: AllType: ObservationalSponsor: Danish Research Centre for Magnetic ResonanceUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

Preterm birth with gestational age below 32 weeks [+12]

Infants have any MRI contraindications, e.g., pacemaker or other implanted elect... [+2]

Status: Recruiting

Infant-Maternal Partnership and Cognitive Training Study for Preterm Infants

This study will test the hypothesis that in preterm infants a caregiver-implemented early developmental intervention (EDI) using finger puppets to develop joint attention and encourage interactive communication with routine EDI care including Bookworm training compared with routine EDI care including Bookworm training alone will increase the Ages and Stages Questionnaire® score at 12 months corrected age.

Participants needed: 188
Trial details
Age: 1-17Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Dec 29, 2025Locations: 1
Eligibility criteria

inborn at UAB, delivered at less than 34 weeks' gestation, 32-39 weeks' PMA, off...

a major malformation, a known syndrome, enrolled in a competing trial targeting...

Status: Recruiting

Effect of Partially Hydrolyzed, Whey-based Infant Formulas on Growth and Tolerability in Healthy Term Infants

This study will assess the effect of partially hydrolyzed, whey-based infant formulas on growth and gastrointestinal tolerance in healthy term infants.

Participants needed: 234
Trial details
Age: 0-28Biological sex: AllType: InterventionalSponsor: Société des Produits Nestlé (SPN)Updated: Dec 19, 2025Locations: 3
Eligibility criteria

Written informed consent has been obtained from at least one parent (or other le... [+6]

Chronic infectious, metabolic, genetic illness or other disease, including any c... [+6]

Status: Recruiting

Behavioral Assessment Method Index

The overall goal of this study is to develop and improve assessment methods for children with and without perinatal arterial ischemic stroke (PAS)/hemiparetic cerebral palsy (HCP). The focus is on behaviors of the arms and hands and includes other domains of child development like fine motor, gross motor, language, cognition, and social-emotional skills. This study involves 1) the use of data, including video recordings, from "I-ACQUIRE - Perinatal Arterial Stroke: A Multi-site RCT of Intensive Infant Rehabilitation" (NCT03910075) and 2) a prospective longitudinal observational data collection with a typically developing cohort using a comprehensive assessment battery (play, fine motor, gross motor, language, cognition, and social emotional skills). The current study is called the BAM Index. No intervention or treatment is provided as part of the BAM Index. The I-ACQUIRE study is an RCT that includes an intervention. The BAM index study is a use of data from the I-ACQUIRE cohorts and a prospective observational study of a typically developing cohort (children without stroke or cerebral palsy) over time. The results of this work will develop, test, refine, and validate a new methodology based on reach-and-grasp and other behaviors related to child development that will have profound and lasting impact on assessment and selection of treatment strategies for pediatric physical rehabilitation of children. The use and reuse of video technology is also well-suited to remote or virtual assessment. This proposal will add to our current knowledge by 1) yielding a psychometrically robust and alternative approach to measuring upper extremity function in children with stroke and/or hemiparetic cerebral palsy and 2) defining specific parameters about how to promote closer-to-normal upper extremity function in children with motor disability.

Participants needed: 80
Trial details
Age: 4-36Biological sex: AllType: ObservationalSponsor: Ohio State UniversityUpdated: Dec 18, 2025Locations: 1
Eligibility criteria

Between 8 and 36 months old at baseline [+2]

Diagnosed or suspected impairments (auditory, visual, cognitive or motor)

Status: Recruiting

Investigating Fit and Satisfaction of the Prone Positioner

The goal of this clinical trial is to learn about the use of the Prone Positioner in pediatric patients with tracheostomies (trachs). The main question\[s\] it aims to answer are: * What is the fit and satisfaction of the device? * Does the device fulfill the goal of allowing infants with trachs participate in tummy time * What aesthetic feedback will the study team receive on the prone positioner from families, therapists, and nursing staff. Participants will be placed in the Prone Positioner, they will be monitored for their comfort/satisfaction with use, and how well they are able to be receive ventilation while in the device. Parents of these infants, as well as healthcare providers, will be surveyed on thoughts/suggestions for the Prone Positioner.

Participants needed: 30
Trial details
Age: 44-24Biological sex: AllType: InterventionalSponsor: Children's Mercy Hospital Kansas CityUpdated: Dec 5, 2025Locations: 1
Eligibility criteria

Inpatient infants located on the Pediatric Intensive Care Unit (PICU) or (Neonat... [+5]

Infants > 24 months of age [+4]

Status: Recruiting

Maternal Abdominal Morphology Assessment

Previous studies have shown that pancreas size tends to be smaller in individuals with diabetes compared to those without diabetes. The investigators have recently found that pancreas size increases during pregnancy. The MAMA study aims to examine changes in the pancreas that occur during pregnancy, in both pregnant mothers and their babies, and find out how they are affected by maternal diabetes. The MAMA study is a prospective cohort study that will follow women and their babies through pregnancy and one year postpartum. Women aged 18-54, who are under 14 weeks pregnant are being recruited to participate in the MAMA study.

Participants needed: 87
Trial details
Age: 18-54Biological sex: FemaleType: ObservationalSponsor: University of Texas at AustinUpdated: Oct 22, 2025Locations: 1
Eligibility criteria

Pregnant women, with a singleton gestation [+4]

Presence of any mechanically or magnetically activated implants [+3]

Status: Recruiting

PANDA Gym: Automated Assessment of Neurodevelopment in Infants at Risk for Motor Disability

Early childhood detection of motor delays or impairments provides the opportunity for early treatment which improves health outcomes. This study will use state of the art sensors combined with machine learning algorithms to develop objective, accurate, easy-to-use tools for the early scoring of deficits and lays the foundation for the early prediction of physical disability.

Participants needed: 1,700
Trial details
Age: 0-6Biological sex: AllType: ObservationalSponsor: University of PennsylvaniaUpdated: Sep 23, 2025Locations: 1
Eligibility criteria

Hydrocephalus [+5]

Status: Recruiting

Talk With Me Baby to Enhance the Early Home Language Environment

The goal of this clinical trial is to learn if the Talk With Me Baby (TWMB) program improves the home-language environment for at-risk families with children ages two to six months when primary care providers deliver the program during well-child checkups. The main question it aims to answer is: Will the TWMB program increase the time a caregiver talks to their infant? Participants will: 1. Come to at least four well-child checkups 2. Receive the TWMB program from the provider during the checkups 3. Record their conversations with their infant before they receive the program and after they receive the program four times.

Participants needed: 66
Trial details
Age: 0-9Biological sex: AllType: InterventionalSponsor: IDeA States Pediatric Clinical Trials NetworkUpdated: Aug 29, 2025Locations: 2
Eligibility criteria

A caregiver who will receive TWMB during routine WCC visits for their child at p... [+8]

Status: Not yet recruiting

Cue-Based Vs. Clinician-Driven Feeding in Very Low Birthweight Infants

In this parallel-group randomized controlled trial, very low birthweight infants will be randomly assigned in a 1:1 ratio to either cue-based (intervention group) or clinician-driven feeding (control group). For infants in the intervention group, Speech therapists and nurses will use their cue-based assessment training to aid in clinical management of oral feeding. For infants in the control group, clinicians caring for these infants will define the feeding plan based on their daily assessment.

Participants needed: 74
Trial details
Age: 28-32Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Aug 15, 2025Locations: 1
Eligibility criteria

Birthweight < 1500 grams [+3]

Major congenital/chromosomal anomalies, [+2]

Status: Recruiting

Walnuts as an Infant Solid Food for Health

The objective is to investigate the effect of walnuts on gut microbiota, inflammatory markers, atopic dermatitis status, and indices of allergy outcomes in breastfed infants during early complementary feeding. The three primary aims include: Aim 1: Evaluate the effect of walnut consumption on gut microbiota structure and function, inflammation, atopic dermatitis, and allergy outcomes. Aim 2: Evaluate the impact of walnut consumption on infant growth trajectories and risk of overweight. Aim 3 (exploratory): Identify walnut-specific food signatures that are associated with gut microbiota and immunity biomarkers using a novel nutri-metabolomics technique.

Participants needed: 90
Trial details
Age: 5-5Biological sex: AllType: InterventionalSponsor: Colorado State UniversityUpdated: Jul 23, 2025Locations: 1
Eligibility criteria

Full term: gestational age ≥ 37 weeks [+3]

Adults unable to consent [+2]

Status: Recruiting

Infant Crying, a Bioacoustic Prognostic Signal for Neurodevelopment

Crying is a vital communication signal for the baby. Product of a complex physiological process, it reflects not only the organization and functioning of the cortical central nervous system and the function of sympathetic and parasympathetic autonomic regulation but also the integrity of three entities: the lungs responsible for ventilatory mechanics and respiratory rhythm, the larynx and its vocal cords as a phonatory organ, and the oropharyngeal tract guaranteeing the resonance of the sound emitted by the vocal cords. Crying is usually caused by pain, discomfort, hunger, or separation from parents or other caregivers. Crying carries essential information from birth, the expression of which depends closely on the neuroanatomical and functional brain integrity of the child. On a bioacoustic level, crying consists of sequences of complex acoustic signals produced by the vocal folds and filtered by the vocal tract. The vibration frequency of the vocal cords determines the cry's fundamental frequency f0 (and the harmonic frequencies), which is responsible for its more or less low or high pitch. Other acoustic cues also characterize each baby's cry.

Participants needed: 1,100
Trial details
Age: Up to 4Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Universitaire de Saint EtienneUpdated: May 28, 2025Locations: 1
Eligibility criteria

For a full-term baby > 37 weeks [+5]

Refusal of participation by the holder of parental authority [+4]

Status: Recruiting

Babies' Brain Responses to Strangers

Researchers at the Diversity in Development Lab at UC Santa Cruz are investigating how babies' brain activities respond to people from familiar and unfamiliar racial backgrounds.

Participants needed: 100
Trial details
Age: 7-12Biological sex: AllType: ObservationalSponsor: University of California Santa CruzUpdated: Mar 6, 2025Locations: 1
Eligibility criteria

typically developing [+2]

any known developmental delays [+1]

Status: Recruiting

Investigating Baby Behavior and Family Technology Use Study

Maternal sensitivity and contingent responsiveness to infant behavioral cues is an important contributor to infants' developing capacities to self-regulate. During early infancy, feeding interactions comprise a significant portion of mother-infant dyadic interactions and high-quality feeding interactions provide both nutritive and socioemotional benefits; recent data suggest that, for many dyads, mothers' sensitive responsiveness during feeding interactions is routinely impacted by the omnipresence of portable technology. The objective of the proposed research is to better understand the development and possible impacts of maternal technology use on infant feeding interactions, emotion and intake regulation, and sociobehavioral and growth outcomes.

Participants needed: 345
Trial details
Biological sex: AllType: InterventionalSponsor: California Polytechnic State University-San Luis ObispoUpdated: Feb 24, 2025Locations: 1
Eligibility criteria

18 years of age or older [+5]

Mother has an untreated medical or psychiatric condition (e.g. bipolar disorder)... [+5]

Status: Recruiting

Families Filming Infants Learning Movement

The study objective is to improve accuracy in the early detection of neurodevelopmental impairment, especially CP, by evaluating the timepoint (in weeks post term age) that the Prechtl GMA is most useful for prediction of neurodevelopmental impairment at two years of age in children with and without medical complexity. The study team plans to recruit 100 healthy, term-born infants and 250 infants at risk of developing CP for a total of 350 enrolled infants.

Participants needed: 350
Trial details
Age: 10-20Biological sex: AllType: ObservationalSponsor: Ann & Robert H Lurie Children's Hospital of ChicagoUpdated: Feb 13, 2025Locations: 1
Eligibility criteria

Infants born full-term with typical development, bithweight >2500g [+7]

Children who are enrolled in DCFS custody [+1]