Language and Motor Skills of Preterm Infants in Pre-school Age: Diagnosis and Early Intervention (LAMOPRESCO)

This study is currently recruiting participants.
Verified January 2013 by University Hospital, Rouen
Sponsor:
Collaborator:
FEDER
Information provided by (Responsible Party):
University Hospital, Rouen
ClinicalTrials.gov Identifier:
NCT01426659
First received: August 29, 2011
Last updated: January 17, 2013
Last verified: January 2013
  Purpose

The preterm children have more difficulty minor neurological developmental than the general population even without cerebral palsy. Their oral language difficulties of language and writing have been little studied. The investigators propose to study spoken language has 3 years 1/2 and stimulate or not (depending on randomization) children with phonological weaknesses notemment language. The investigators will evaluate stimulation protocol implied short and precise language in a re-education "say and do" in 20 sessions. A new evaluation of language (BILO and N-EEL), sensorimotor and cognitive constraints (KABC) will be performed at 4 years.

Early intervention on the basis of precise language before closing the window developmental (<5 years) is expected to improve as a result of language and cognitive development of preterm infants.


Condition Intervention
Disorder of Speech and Language Development
Behavioral: parental stimulation according to protocol

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Evaluation of Language and Sensorimotor Constraints of Very Premature Babies at the Age of 3 Years 1 / 2 Without Cerebral Palsy. Randomised Study of Stimulation Training Implicit in Children Vulnerable

Resource links provided by NLM:


Further study details as provided by University Hospital, Rouen:

Primary Outcome Measures:
  • parental endorsement of stimulation [ Time Frame: for at least 15 weeks ] [ Designated as safety issue: No ]
    stimulation every day image of the Protocol


Secondary Outcome Measures:
  • come following a speech therapy every week [ Time Frame: 15 weeks ] [ Designated as safety issue: No ]
    constructive working session of 30 minutes according to the protocol say and do


Estimated Enrollment: 296
Study Start Date: September 2011
Estimated Study Completion Date: August 2014
Estimated Primary Completion Date: February 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Protocol "say and do"
reeducation implicit 5 minutes every day at home and 30 minutes of speech therapy every week
Behavioral: parental stimulation according to protocol
verbal stimulation every day image of the Protocol "Dire et Faire"
Active Comparator: no stimulation "say and do" Behavioral: parental stimulation according to protocol
verbal stimulation every day image of the Protocol "Dire et Faire"

  Hide Detailed Description

Detailed Description:

Very premature babies born before 32 weeks gestation have developmental problems more important than the rest of the population. The study reported 40% Epipage neuromotor difficulties of varying severity. Children with cerebral palsy are down 9% to 6%. However the rate of minor neurological problems and school failure is increasing. Neurocognitive difficulties are many, visuospatial dyspraxia, attention disorders, language impairment. The latter is fairly described in the literature and seems often seen in this population in relation to overall cognitive difficulties. Cognitive assessments of the overall K-ABC of former premature study Epipage are nevertheless often normal. Oral language is fundamental to the written language and learning at school and follows a mature development stages according to specific sensorimotor well known. The investigators hypothesize that minor sensorimotor disorders in the population of premature infants without CP can change structurally and early oral language, including phonology. Accurate assessment of the components of language at 3 years of premature children without CP or neurosensory disorder found (blindness, deafness) has already allowed us to observe weaknesses in the structural components of language. These early failures may correspond to a particular neurological architecture of language observed in functional MRI in the same population of children aged 8 and 12 years (Schaer 2009, Petterson 2002) and may be sensitive to a specific stimulation early before the developmental window architecture of the spoken language is closed (Newport 2002).

Objective: To evaluate the interest of accurate and early stimulation implied short ("say and do") on areas of weakness in the language 3ans1 / 2 of the former preterm infants without CP spotted by BILO.

Method: This is a prevention trial national, multicenter, prospective randomized two arms. In this study, 296 patients with premature frailty of oral language without CP, with or without minor neurological disorder, and without proven pathology of oral language will be included in 5 hospitals and will be randomized to receive or not a specific stimulation (say and do " ). The assessment of oral language by a Computerized Assessment BILO1 (Khomsa 2008) ½ to 3 years will be offered to all parents of children with CP followed without neurosensory disorder or current fact. After obtaining consent, and results BILO, directed by a therapist trained in order to define the criteria for frailty, randomization will be done centrally. Early stimulation precise and short (20 therapy sessions per week) on these areas of weaknesses of language drive will be compared to the absence of specific stimulation. Evaluation at 6 months results will be blinded.

Inclusion is scheduled 24 months for the inclusion of patients with results defining areas of weakness in BILO1dans one of the components of language: an item <10th percentile and / or two items <25th percentile). .

Excluding children with pathological scores BILO1 (<3rd percentile for at least one criterion) will not be included Primary endpoint: difference from baseline and after six months of phonology BILO score (score from 0 to 16 listed) Number of subjects and statistical power: 170 children a year born very preterm live out the CHU of Rouen. One hundred are followed and accept the studies conducted in the service as in other centers who collaborated in the study EPIPAGE (Lancet 2008). According to our preliminary work half the present language problems at 3 years. Thus, 50 children per year would be candidates for the study but 10% are pathological oral language and therefore excluded from the study. 296 children were included in five centers and according to their follow-up rate according to these proportions. Three centers have follow-up of very preterm and 80/an a regional 30/an. According to preliminary data, and assuming a moderate correlation of 0.5 between BILO scores at baseline and after six months, the standard deviation of the primary endpoint was 4.7 units of phonology BILO score. Thus, to test the risk of first kind of b = 5% in bilateral formulation, the total of 296 children included and evaluated (or 148 children per group) to detect with a statistical power of 90%, size effect of 0.379, a difference of 1.8 units average score BILO groupes. Ainsi between the two, the number chosen to detect with a high power low difference between the two groups for the primary .

Statistical analysis: The means of the primary endpoint will be compared between groups by one-tailed t test at the usual 5%. This test will be completed by comparing adjusted based on multiple linear regression model taking into account possible prognostic factors (duration of gestation, bronchopulmonary dysplasia, neurological disorders minors, socio-economic status ...), the center and the initial value ( to 3 years) score phonology. The difference in means between two groups and its confidence interval 95% will be estimated.

Outlook: Creating a cohort followed to analyze the impact of early stimulation specific to the age of 6 and assess our level of prevention of disorders of oral and written language.

  Eligibility

Ages Eligible for Study:   34 Months to 38 Months
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Premature < 32 without CP,
  • criteria of fragility BILO

Exclusion Criteria:

  • blindness,
  • deafness,
  • abnormal karyotype results in normal or pathological BILO
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01426659

Contacts
Contact: A Charollais 0232885693 ext 0033 aude.charollais@chu-rouen.fr
Contact: A Charollais 0232888099 ext 0033 aude.charollais@chu-rouen.fr

Locations
France
University Hospital Recruiting
Rouen, Haute Normandie, France, 76000
Contact: Aude Charollais, Doctor     0232888097 ext 68700     aude.charollais@chu-rouen.fr    
Contact: Stéphane Marret, Professor     0232888097 ext 66422     stephane.marret@chu-rouen.fr    
University Hospital Recruiting
Caen, France, 14033
Contact: Bernard Guillois, Professor     02 31 27 25 64     guillois-b@chu-caen.fr    
University Hospital Recruiting
Grenoble, France, 38 043
Contact: Thierry Debillon, Professor     04 76 76 55 77     Tdebillon@chu-grenoble.fr    
University Hospital Recruiting
Le Havre, France, 76600
Contact: Benoit Delaporte, Doctor     02 32 73 36 20     benoit.delaporte@ch-havre.fr    
Contact: Henri Bruel, Doctor     02 32 73 36 20     henri.bruel@ch-havre.fr    
Centre Jacques Cartier Recruiting
St Brieuc, France, 22070
Contact: Anne Busnel, Doctor     02.96.01.71.29     anne.busnel@ch-stbrieuc.fr    
University Hospital Recruiting
Tours, France, 37000
Contact: Eli Saliba, Professor     02 47 47 47 56     saliba@med.univ-tours.fr    
Sponsors and Collaborators
University Hospital, Rouen
FEDER
Investigators
Principal Investigator: A Charollais UH Rouen
  More Information

Publications:
Responsible Party: University Hospital, Rouen
ClinicalTrials.gov Identifier: NCT01426659     History of Changes
Other Study ID Numbers: 2010/089/HP
Study First Received: August 29, 2011
Last Updated: January 17, 2013
Health Authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

Keywords provided by University Hospital, Rouen:
language
constraints
premature
phonology
implied
early development (< 5 years)

ClinicalTrials.gov processed this record on May 19, 2013