Study Results
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Basic Information
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ENROLLING_BY_INVITATION
NA
140 participants
INTERVENTIONAL
2023-08-06
2025-12-31
Brief Summary
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To examine cognition, motor function, executive functions, speech and language development, behaviour, psychosocial functioning,academic achievement, physical morbidities and growth of MLPTI at the age of 9 years and correlate this with BSID-III-NL scores,growth parameters and body composition at the age of 2 years.
Study design:
This study will be a prospective open, non-therapeutic exploratory cohort study and can be seen as a continuation on the study with protocol identification number NL50800.094.14, performed in the NWZ Alkmaar between 2014 and 2016. This was a study on growth and neurodevelopment of MLPTI in the first 2 years of life.
Study population:
The study population is a group of 200 moderate and late preterm children who were born in the NWZ Alkmaar between 2014 and 2016. 100 of these children participated in the aforementioned study on growth and neurodevelopment at the age of 2 years. The oldest children in this group will reach the age of 9 years in 2023. Brothers/sisters/friends of these children aged between 8 and 10 will be asked as control group (n=50).
Primary study parameters/outcome of the study:
The main study parameters are the IQ-scores of the WISC-V, the motoric scores of the Movement-ABC, the executive functions of the EMMA Toolbox, the presence of morbidities, the growth pattern and the mean blood pressure at 9 years of age.
Secondary study parameters/outcome of the study:
Secondary outcome parameters are the he behavioural and psychosocial outcomes of the CBCL and the SDQ scores, speech-and language-developmental scores of the CELF-5-NL and CCC-2-NL, MCH Feeding Scale and Teacher Report Form (TRF) scores. Other outcome parameters are the relation between the 9-year outcomes and the BSID-III scores at the age of 2, and the differences between the MLPTI and the control group. Furthermore, we aim to determine the relation between growth and body composition in the first two years of life and the waist circumference, growth parameters and blood pressure at the age of 9 years.
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Detailed Description
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In addition, one recent study correlated impaired behavioural outcomes and lower IQ-scores at the age of 6 with the attentional and language scores of a Bayley Scales of Infant and Toddler Development (BSID-III) performed at the age of 1.5 to 2 years. This relation, however, is not confirmed in other studies. More research is therefore necessary to clarify the predictive value of these screening methods in early detection of impaired outcomes during school age, and to examine whether a longer follow-up could thereby help to prevent these problems.
Objective: To assess neurodevelopmental outcomes (including neurocognitive, motor, language, behavioral, and academic functioning), growth and morbidities in MLPTI children at the age of 9 born in the NWZ Alkmaar, and compare these outcomes to those of a sex and age-matched control group of friends of MLPTI children born at uncomplicated full term gestational age.
Study design: This study will be a prospective open, non-therapeutic exploratory cohort study and can be seen as a continuation on the study with protocol identification number NL50800.094.14, performed in the NWZ Alkmaar between 2014 and 2016. That study described growth, body composition and neurodevelopmental outcome of MLPTI in the first 2 years of life.
Study population: The study population is a group of 200 moderate and late preterm children who were born in the NWZ Alkmaar between 2014 and 2016. A total number of hundred children participated in the aforementioned study on growth and neurodevelopment at the age of 2 years. The oldest children of this cohort will reach the age of 9 years in January 2023. Sex and age-matched friends of these children whom are also 9 years old will be examined as control group of same aged peers (n=70).
Intervention: Parents will be asked to fill in five widely used questionnaires, including the Child Behaviour Checklist (CBCL), Strengths and Difficulties Questionnaire (SDQ), Childrens Communication Checklist (CCC-2-NL), Montreal Childrens Hospital Feeding Scale (MCH Feeding Scale) and a custom made questionnaire on morbidities. Teachers will be asked to complete the Teacher report form (TRF)), which is a version of the CBCL adapted for teachers. Children will visit the outpatient clinic once for neurodevelopmental assessment, including the Wechsler Intelligence Scale of Development for Children (WISC-V-NL) to assess intelligence (IQ), the EMMA-Toolbox to assess neurocognitive functioning, the Movement ABC (MABC-II-NL) to assess motor function, and subtests of the Clinical Evaluation of Language Fundamentals (CELF-5-NL) to assess language development. Furthermore, academic achievement will be assessed using existing data collected at school as part of the student monitoring system (National Institute for Educational Measurement (CITO)). During the same single visit, length, weight, waist circumference and blood pressure will be measured to analyse the body composition.
Main study parameters/endpoints: To examine neurodevelopmental outcomes (including neurocognitive, motor, language, and (eating-)behavioral function, and academic achievement), growth and morbidities in MLPTI children at the age of 9 born in the Noordwest Ziekenhuis, location Alkmaar, and compare them with a control group of 9 year old friends born at full term.
Secondary study parameters/outcome of the study:
Secondary outcome parameters are the he behavioural and psychosocial outcomes of the CBCL and the SDQ scores, speech-and language-developmental scores of the CELF-5-NL and CCC-2-NL, The Montreal Children Hospital feeding Scale and Teacher Report Form scores. Other outcome parameters are the relation between the 9-year outcomes and the BSID-III scores at the age of 2, and the differences between the MLPTI and the control group. Furthermore, we aim to determine the relation between growth and body composition in the first two years of life and the waist circumference, growth parameters and blood pressure at the age of 9 years.
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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MLPTI Cohort
Group of 9 year old children born between 32 and 36 weeks of gestational age
CBCL
A questionnaire on behaviour
SDQ
A questionnaire on behaviour
CCC-2-NL
A questionnaire on communcational skills
MCH Feeding scale
A questionnaire on feeding problems
TRF
A questionnaire on behaviour
WISC-5-NL
An IQ test for children
Movement ABC
A test to assess motor function
CELF-5-NL
A test to assess language development
Emma Toolbox
Test of executive functions
Control cohort
Group of 9 year old children born at term
CBCL
A questionnaire on behaviour
SDQ
A questionnaire on behaviour
CCC-2-NL
A questionnaire on communcational skills
MCH Feeding scale
A questionnaire on feeding problems
TRF
A questionnaire on behaviour
WISC-5-NL
An IQ test for children
Movement ABC
A test to assess motor function
CELF-5-NL
A test to assess language development
Emma Toolbox
Test of executive functions
Interventions
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CBCL
A questionnaire on behaviour
SDQ
A questionnaire on behaviour
CCC-2-NL
A questionnaire on communcational skills
MCH Feeding scale
A questionnaire on feeding problems
TRF
A questionnaire on behaviour
WISC-5-NL
An IQ test for children
Movement ABC
A test to assess motor function
CELF-5-NL
A test to assess language development
Emma Toolbox
Test of executive functions
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* The participant is born in or transferred to the NWZ Alkmaar between January 1st, 2014 and April 18th, 2016 (the time in which the participants of trial NL50800.094.14 were born).
* The participant born at a gestational age from 32 to 35+6 weeks.
* Both parents of the participant have given informed consent to participate in the 9 years trial
In order to be eligible to participate in the control group of this study, a subject must meet all the following criteria:
* The participant is 9 years old when participating in this study and is a friend or classmate of the included MLPTI.
* Both parents of the participant have given informed consent for the participation of the study.
Exclusion Criteria
* The participant's parents are not able to fill out questionnaires or perform tests in Dutch.
* The participant has a severe developmental or genetic disorder and is thereby not able to perform the tests.
* The participant is not able to come to the outpatient clinic to do the tests.
A potential subject who meets any of the following criteria will be excluded from participation in this study as part of the control group:
* The participant is born with a GA \< 37 weeks.
* The participant has a severe developmental or genetic disorder and is thereby not able to perform the tests.
* The participant had complications after birth (e.g. admission at a Neonatal ward)
* The participant needs special education
9 Years
9 Years
ALL
Yes
Sponsors
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Noordwest Ziekenhuisgroep
OTHER
Responsible Party
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F. (Femke) de Groof
Principal Investigator, MD, PhD
Principal Investigators
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METC AUMC
Role: STUDY_CHAIR
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Locations
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Noordwest Ziekenhuisgroep
Alkmaar, , Netherlands
Countries
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Other Identifiers
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NL82197.029.22
Identifier Type: -
Identifier Source: org_study_id
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