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dc.contributor.authorHoei-Hansen, Christina Engel
dc.contributor.authorWeber, Lene
dc.contributor.authorJohansen, Mette
dc.contributor.authorFabricius, Rebecca
dc.contributor.authorHansen, Jonas Kjeldbjerg
dc.contributor.authorViuff, Anne-Cathrine F.
dc.contributor.authorRønde, Gitte
dc.contributor.authorHahn, Gitte Holst
dc.contributor.authorØstergaard, Elsebet
dc.contributor.authorDuno, Morten
dc.contributor.authorLarsen, Vibeke Andrée
dc.contributor.authorMadsen, Camilla Gøbel
dc.contributor.authorRøhder, Katrine
dc.contributor.authorElvrum, Ann-Kristin Gunnes
dc.contributor.authorLaugesen, Britt
dc.contributor.authorGanz, Melanie
dc.contributor.authorMadsen, Kathrine Skak
dc.contributor.authorWillerslev-Olsen, Maria
dc.contributor.authorDebes, Nanette Mol
dc.contributor.authorChristensen, Jan
dc.contributor.authorChristensen, Robin
dc.contributor.authorRackauskaite, Gija
dc.date.accessioned2024-02-08T14:17:38Z
dc.date.available2024-02-08T14:17:38Z
dc.date.created2023-11-10T08:35:21Z
dc.date.issued2023
dc.identifier.citationBMC Pediatrics. 2023, 23 (1), .en_US
dc.identifier.issn1471-2431
dc.identifier.urihttps://hdl.handle.net/11250/3116429
dc.description.abstractBackground Early diagnosis of cerebral palsy (CP) is important to enable intervention at a time when neuroplasticity is at its highest. Current mean age at diagnosis is 13 months in Denmark. Recent research has documented that an early-diagnosis set-up can lower diagnostic age in high-risk infants. The aim of the current study is to lower diagnostic age of CP regardless of neonatal risk factors. Additionally, we want to investigate if an early intervention program added to standard care is superior to standard care alone. Methods The current multicentre study CP-EDIT (Early Diagnosis and Intervention Trial) with the GO-PLAY intervention included (Goal Oriented ParentaL supported home ActivitY program), aims at testing the feasibility of an early diagnosis set-up and the GO-PLAY early intervention. CP-EDIT is a prospective cohort study, consecutively assessing approximately 500 infants at risk of CP. We will systematically collect data at inclusion (age 3–11 months) and follow a subset of participants (n = 300) with CP or at high risk of CP until the age of two years. The GO-PLAY early intervention will be tested in 80 infants with CP or high risk of CP. Focus is on eight areas related to implementation and perspectives of the families: early cerebral magnetic resonance imaging (MRI), early genetic testing, implementation of the General Movements Assessment method, analysis of the GO-PLAY early intervention, parental perspective of early intervention and early diagnosis, early prediction of CP, and comparative analysis of the Hand Assessment for Infants, Hammersmith Infant Neurological Examination, MRI, and the General Movements method. Discussion Early screening for CP is increasingly possible and an interim diagnosis of “high risk of CP” is recommended but not currently used in clinical care in Denmark. Additionally, there is a need to accelerate identification in mild or ambiguous cases to facilitate appropriate therapy early. Most studies on early diagnosis focus on identifying CP in infants below five months corrected age. Little is known about early diagnosis in the 50% of all CP cases that are discernible later in infancy. The current study aims at improving care of patients with CP even before they have an established diagnosis.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleCerebral Palsy – Early Diagnosis and Intervention Trial: protocol for the prospective multicentre CP-EDIT study with focus on diagnosis, prognostic factors, and interventionen_US
dc.title.alternativeCerebral Palsy – Early Diagnosis and Intervention Trial: protocol for the prospective multicentre CP-EDIT study with focus on diagnosis, prognostic factors, and interventionen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber0en_US
dc.source.volume23en_US
dc.source.journalBMC Pediatricsen_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s12887-023-04312-7
dc.identifier.cristin2194859
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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