Premature Birth Clinical Trial
Official title:
Early Intervention in Preterm Infants: Effects of a Parental Training Program on Neonatal Brain Development, Visual Functions and Neurobehavioral Outcome
| NCT number | NCT02983513 |
| Other study ID # | MITP Preterm |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | April 2014 |
| Est. completion date | January 2023 |
| Verified date | February 2023 |
| Source | Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Preterm infants, during their stay in the Neonatal Intensive Care Unit (NICU), face a period of stressful environment, which may negatively impact early brain development and subsequent neurobehavioral outcomes. This study aims to assess the effectiveness of training parents in reducing stressful experiences early in life and in enhancing brain development and long term developmental outcomes.
| Status | Completed |
| Enrollment | 70 |
| Est. completion date | January 2023 |
| Est. primary completion date | April 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 25 Weeks to 29 Weeks |
| Eligibility | Inclusion Criteria: - Gestational age between 25+0 and 29+6 weeks Exclusion Criteria: - major brain lesions as documented by cranial ultrasound (intraventricular hemorrhage > 2 grade, cystic periventricular leukomalacia) - neurosensorial deficits (retinopathy of prematurity > stage 2) - genetic syndromes and/or major congenital malformations - major neonatal comorbidities Mothers are selected according to the following inclusion criteria: age over 18 years, good comprehension of Italian language, no obvious cognitive impairments or psychiatric disorders, no drug addiction and no single-parent families. |
| Country | Name | City | State |
|---|---|---|---|
| Italy | NICU, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico | Milan |
| Lead Sponsor | Collaborator |
|---|---|
| Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico |
Italy,
Guzzetta A, D'Acunto MG, Carotenuto M, Berardi N, Bancale A, Biagioni E, Boldrini A, Ghirri P, Maffei L, Cioni G. The effects of preterm infant massage on brain electrical activity. Dev Med Child Neurol. 2011 Sep;53 Suppl 4:46-51. doi: 10.1111/j.1469-8749.2011.04065.x. — View Citation
Newnham CA, Milgrom J, Skouteris H. Effectiveness of a modified Mother-Infant Transaction Program on outcomes for preterm infants from 3 to 24 months of age. Infant Behav Dev. 2009 Jan;32(1):17-26. doi: 10.1016/j.infbeh.2008.09.004. Epub 2008 Nov 20. — View Citation
Provenzi L, Fumagalli M, Sirgiovanni I, Giorda R, Pozzoli U, Morandi F, Beri S, Menozzi G, Mosca F, Borgatti R, Montirosso R. Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants. Front Behav Neurosci. 2015 Apr 21;9:99. doi: 10.3389/fnbeh.2015.00099. eCollection 2015. — View Citation
Ricci D, Cesarini L, Romeo DM, Gallini F, Serrao F, Groppo M, De Carli A, Cota F, Lepore D, Molle F, Ratiglia R, De Carolis MP, Mosca F, Romagnoli C, Guzzetta F, Cowan F, Ramenghi LA, Mercuri E. Visual function at 35 and 40 weeks' postmenstrual age in low-risk preterm infants. Pediatrics. 2008 Dec;122(6):e1193-8. doi: 10.1542/peds.2008-1888. — View Citation
Ricci D, Romeo DM, Serrao F, Cesarini L, Gallini F, Cota F, Leone D, Zuppa AA, Romagnoli C, Cowan F, Mercuri E. Application of a neonatal assessment of visual function in a population of low risk full-term newborn. Early Hum Dev. 2008 Apr;84(4):277-80. doi: 10.1016/j.earlhumdev.2007.10.002. Epub 2007 Nov 8. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Neonatal Visual Assessment Battery to evaluate visual function | Neonatal Visual Function is assessed using the Visual Assessment Battery developed by Ricci et al. The assessment evaluates the following items: Ocular spontaneous motility, ability to fix and follow a target, reaction to colour, visual acuity and visual attention at distance. Each item is scored as normal (score 0) or abnormal (score 1). The global score is then calculated as the sum of all the individual items, as designed by the authors. | 40 weeks postmenstrual age | |
| Primary | Neonatal Behavior | Neonatal behavior is assessed using the Neonatal Behavior Assessment Scale that evaluates: habituation, social-interactive, motor system, state organization and regulation, autonomic system, reflexes. | 2 months corrected age | |
| Secondary | Brain development | Conventional and advanced MRI | 40 weeks postmenstrual age | |
| Secondary | Developmental outcome | Children development is assessed using the Bayley Scales of Infant and Toddlers (Third edition) - including: cognitive, motor, language, social-emotional and adaptive behavior) | 24 months corrected age | |
| Secondary | Epigenetic changes | epigenetic analysis is performed at birth on a cord blood sample (0.5 ml) and at hospital discharge on a peripheral blood sample (0.5 ml) collected according routine clinical procedures | up to 48 weeks gestational age | |
| Secondary | overall duration of hospitalisation | number of days from admission to home discharge from NICU | up to 48 weeks gestational age | |
| Secondary | Weight (in grams) at 40 weeks postmenstrual age | 40 week gestational age | ||
| Secondary | Length(in centimeters) at 40 weeks postmenstrual age | 40 week gestational age | ||
| Secondary | Head circumference (in centimeters) at 40 weeks postmenstrual age | 40 week gestational age | ||
| Secondary | Acquisition of full oral feeding | Postmenstrual age at the acquisition of full oral feeding | up to 48 weeks gestational age | |
| Secondary | Feeding with Human milk | Feeding with human milk at 40 weeks postmenstrual age (yes or no) | up to 40 weeks gestational age | |
| Secondary | Neurodevelopmental outcome | Children neurodevelopment is assessed using the Griffiths Development Scales (GMDS).
Scores range from 50 to 150 General quotient mean 100 SD 12, sub scales mean 100 SD 16 Higher scores mean a better outcome |
5-6 years of age | |
| Secondary | Behavioral outcome | Children behavior is assessed using the Child Behavior Checklist. A T score above 70 is considered to be in the clinical range, a T score between 65 an 70 is considered borderline while a T score below 65 is considered normal | 5-6 years of age | |
| Secondary | Neuromotor outcome | Children neuromotor is assessed using the Movement Assessment Battery for Children (Movement ABC).
A score above 67 is considered to be in the normal range, a score between 57 an 67 is considered borderline while a score below 56 is considered pathological |
5-6 years of age | |
| Secondary | Attention outcome | Child attention abilities is assessed using the Early Childhood Attention Battery (ECAB).
Scaled scores range from 1 to 19. Lower scores indicate worst outcome |
5-6 years of age | |
| Secondary | L1 promoter methylation levels on buccal swab | epigenetic analysis - L1 promoter methylation (Percent) assessment is performed on a buccal swab collected at follow-up assessment at 5-6 years. | 5-6 years of age |
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