Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03700463
Other study ID # RC18_0147
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 16, 2018
Est. completion date June 15, 2019

Study information

Verified date August 2019
Source Nantes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Preterm children have a high risk for neurodevelopmental impairments. The impact on motor functions and neurosensory functions is demonstrated but the incidenceof executive functions is not described for preterm infants.


Description:

It is an epidemiologic, observational, prospective study. All patients, included in the LIFT cohort, in 3 to 4 year old during the period study, are contacted by mail. Patientswith congenital anomalies or genetic syndromes are excluded. Children with parents who do not speak French are excluded. Antenatal and postnatal criteria known to be associated with disorders of executive functions are collected as, gestational age, sex, multiple pregnancy, intrauterine growth retardation, antenatal or postnatal steroid use, breastfeeding, cerebral injuries and socio-economic status. After a couple of weeks, parents are contacted by a study manager, by phone call, to collect parental consent and answer parental questions. After consent collect, BRIEF questionnaires are sending. If they wish, parents could give the BRIEF teacher questionnaire to the mean teacher. Teachers send by themselves their response. An informatic version is available with a personal link given especially by mail for each child. All data are anonymous. BRIEF questionnaire is composed of 63 items, exploring 2 main domains: behavior and metacognition. Twenty minutes are necessary to complete questionnaire. In case of no questionnaire return after one month, parents are contacted by phone. The investigators hypothesize a lost to follow-up at 0.25 and no response at 0.35. The response expected is 300 questionnaires.


Recruitment information / eligibility

Status Completed
Enrollment 356
Est. completion date June 15, 2019
Est. primary completion date June 15, 2019
Accepts healthy volunteers
Gender All
Age group 3 Years to 4 Years
Eligibility Inclusion Criteria:

- patient in 3 to 4 year old, included in LIFT cohort

Exclusion Criteria:

- Congenital abnormalities including nervous system malformations; genetic diseases; incomplete understanding of written and oral French by parents

Study Design


Related Conditions & MeSH terms


Intervention

Other:
BRIEF parental survey
Estimate incidence of executive functions disorders in preterm children in 3 to 4 year old, born less than 34 weeks of gestation

Locations

Country Name City State
France CHU Nantes Nantes

Sponsors (2)

Lead Sponsor Collaborator
Nantes University Hospital University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of disorders of executive functions in 3 to 4 year old which former preterm of gestational age less than 34 weeks, from the Behavioral Rating Inventory of Executive Function questionnaire. sum of 63 items is calculated 3 to 4 years after preterm birth
Secondary neonatal factors Neonatal factors associated with executive functions disorders in former prematures in 3 to 4 year old and adequacy between BRIEF questionnaire performed/completed by parents and BRIEF questionnaire performed by teacher. 3 to 4 years after preterm birth
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04062513 - Olfactive Stimulation Interventions With Mothers' Milk on Preterm Pain Response N/A
Completed NCT03412578 - Effect of Tactile/Kinaesthetic Massage Therapy on DXA Parameter of Preterm Infants N/A
Completed NCT03166722 - Cerebral Regional Tissue Oxygen Saturation to Guide Oxygen Delivery in Preterm Neonates During Immediate Transition N/A
Enrolling by invitation NCT03212547 - The Effect of a Neonatologist's Standardized Guidance Intervention on Preterm Infants With Relational Withdrawal. N/A
Completed NCT03931902 - The Comparison of Laryngeal Mask Airway and Endotracheal Tube in General Anesthesia for Premature Neonates N/A
Completed NCT03302000 - Visual Stimulation of Preterm Infants N/A
Completed NCT03731546 - Effect of Delayed Cord Clamping in Preterm Neonates With Placental Insufficiency N/A
Completed NCT03104946 - To Research the Relation Between Neonatal Morbidities and Poor Outcome in Preterm Infants N/A
Completed NCT03704012 - Efficacy of Massage Applied by the Parents in Hospitalized Premature Birth (PreMas) N/A
Suspended NCT03220282 - The Milk, Growth and Microbiota Study N/A
Active, not recruiting NCT03232931 - Trial to Improve Multisensory Neural Processing, Language & Motor Outcomes in Preterm Infants N/A
Completed NCT03242057 - Comparison of Primary Extubation Failure Between NIPPV and NI-NAVA N/A
Completed NCT04089540 - New Intubation Method to Achieve Circulatory Stability and to Reduce Number of Intubation Attempts in Neonates N/A
Not yet recruiting NCT02528851 - Cardiorespiratory Effects of "Higher" Versus "Equivalent" CPAP Upon Extubation From High EAP in Preterm Infants N/A
Completed NCT01959737 - Delivery Room Skin-to-skin Study N/A
Completed NCT02811432 - Kangaroo Mother Care Before Stabilisation Amongst Low Birth Weight Neonates in Africa N/A
Completed NCT03728764 - Growth and Safety of a Two-stage Feeding System in Preterm Infants N/A
Completed NCT04382976 - The Incidence and the Risk Factors of Nephrocalcinosis in Very Preterm Infants
Completed NCT03748914 - C-UCM and Cerebral Oxygenation and Perfusion N/A
Completed NCT05815706 - The Effect of the SNS-Based Feeding on Transition to Exclusive Breastfeeding in Preterm Infants N/A