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| Name | Class |
|---|---|
| Coombe Women and Infants University Hospital | OTHER |
| The Rotunda Hospital | OTHER |
| Cerebral Palsy Foundation | UNKNOWN |
| Karolinska Institutet |
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Cerebral palsy (CP) is a condition when a baby has a brain injury that affects their movement and muscle tone. Some people with CP can have other developmental issues, like learning impairments, but many do not and have isolated issues with their motor skills. Some newborns are at higher risk of developing CP, including babies born prematurely, those who have an injury to their brain, and those who have an abnormal neurological examination. However, most babies with a higher risk of CP do not develop CP. The problem is that doctors can't tell early on who will and who will not develop CP, they can only say who has a risk of it. Therefore, these babies are followed up in out-patient clinics to see how they are progressing, usually by a neonatologist (baby doctor), often a physiotherapist, and some may also be referred to services in the community like the Early Intervention Team. If there is a significant concern, doctors will often perform a scan of the baby's brain to provide more information. Even with all this follow-up, it still usually takes at least 12 months, and can be up to 2 years, to diagnose a child as having CP.
In this study the aim is to try and reduce the age of diagnosis of CP by assessing children in high-risk out-patient clinics using novel and specific examinations. We would also like to improve our ability to predict who will need help with learning, language or other non-motor outcomes. This study is being conducted at several hospitals in Ireland, including Cork University Maternity Hospital (CUMH), The Rotunda Hospital and the Coombe Women and Infants Hospital. It is being coordinated by the In4kids network and will be conducted in the INFANT Centre/ University College Cork (UCC). The study has been funded by Research Ireland and the Cerebral Palsy Foundation, USA.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| High-Risk Group | This group will have risk factors such as prematurity or hypoxic-ischaemic encephalopathy which put them in the High-Risk cohort | ||
| Control Group | This group will be healthy, term infants who do not require admission to neonatal intensive care |
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| Measure | Description | Time Frame |
|---|---|---|
| A | To characterise the development of neural architecture and function during sleep using EEG, from the near-term period to 4 months corrected gestational age for infants at elevated risk of cerebral palsy and diagnosed with cerebral palsy | From near term to 4 months corrected gestational age |
| B | To examine underlying neuro-specific protein profiles near term corrected gestational age as early biomarkers of altered neural function, motor and developmental outcomes in infants at elevated risk of cerebral palsy and diagnosed with cerebral palsy. | Birth to 6 weeks |
| C | Develop novel measures of cognitive outcome, including executive function, and use these to compare trajectories in infants with cerebral palsy and those without, from 4 to 24 months | 4 to 24 months |
| Measure | Description | Time Frame |
|---|---|---|
| A | To optimise existing predictive machine learning algorithms | During the study period, ie. over five years |
| B | To develop and establish a standardised, early fixation classification assessment tool that can be used for infants at risk of cerebral palsy in high-risk follow-up clinics across Ireland |
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Inclusion Criteria (High Risk Group) :
Legal guardians must be able and willing to give written informed consent and to comply with the requirements of this study protocol.
All infants considered high risk for a diagnosis of cerebral palsy and neuro-developmental impairment will be eligible, specifically including:
(Control Group)
-A control arm will also be recruited.
Exclusion Criteria:
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All infants considered high risk for a diagnosis of cerebral palsy and neuro-developmental impairment will be eligible, specifically:
All preterm infants born ≤32 weeks Post Menstrual Age or ≤1500 gm birth weight
All encephalopathic infants
Neurological risk factors (e.g., injury/malformation on neuroimaging, persistently abnormal neurological exam)
All full-term infants (>37 weeks gestation), without requirement for admission to the NICU will be eligible to be enrolled in the study as the control arm of the study
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Deirdre Murray Principal Investigator | Contact | +353 021 420 5082 | d.murray@ucc.ie | |
| Danielle Clifford | Contact | +353 021 420 5082 | dclifford@ucc.ie |
| Name | Affiliation | Role |
|---|---|---|
| Deirdre M Murray | INFANT Research Centre, University College Cork, Cork, Ireland | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cork University Maternity Hospital | Recruiting | Cork | Ireland |
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| Label | URL |
|---|---|
| Launch of Cerebral Palsy Research Programme at University College Cork | View source |
| Inaugural lecture: Professor Deirdre Murray, CPF Chair in Early Brain Injury and Cerebral Palsy | View source |
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Individual Patient Data may not be shared according to ethical approval
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| OTHER |
| University of Pisa | OTHER |
| Göteborg University | OTHER |
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Microsampling will be used to collect samples from high-risk infants in the neonatal unit. These will be used for biomarker analysis including neurospecific proteins and mRNA.
| 4 months |
| C | To investigate ophthalmological biomarkers, including morphology, as potential early predictors of cerebral palsy and cognitive outcomes | 18 months |
| INFANT Centre, University College Cork | Recruiting | Cork | Ireland |
|
| Coombe Women and Infant's Hospital | Not yet recruiting | Dublin | Ireland |
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| The Rotunda Hospital | Recruiting | Dublin | Ireland |
|
| Cerebral Palsy advocate Lily Collison receives honorary doctorate from UCC | View source |
| ID | Term |
|---|---|
| D002547 | Cerebral Palsy |
| D002658 | Developmental Disabilities |
| D047928 | Premature Birth |
| D060825 | Cognitive Dysfunction |
| D020925 | Hypoxia-Ischemia, Brain |
| ID | Term |
|---|---|
| D001925 | Brain Damage, Chronic |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D065886 | Neurodevelopmental Disorders |
| D001523 | Mental Disorders |
| D007752 | Obstetric Labor, Premature |
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D003072 | Cognition Disorders |
| D019965 | Neurocognitive Disorders |
| D002545 | Brain Ischemia |
| D002561 | Cerebrovascular Disorders |
| D002534 | Hypoxia, Brain |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D000860 | Hypoxia |
| D012818 | Signs and Symptoms, Respiratory |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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