The Alkmaar MLPTI Cohort Study: Outcomes at 9 Years

NCT ID: NCT05990582

Last Updated: 2023-08-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

140 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-08-06

Study Completion Date

2025-12-31

Brief Summary

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Objective of the study:

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.

Detailed Description

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SUMMARY Rationale: Recent studies indicate that moderate and late preterm infants (MLPTI, gestational age (GA) 32-36 weeks) are at risk of lower IQ scores, behavioural and attention problems and academic underachievement at the age of 6 to 10 years. These recent findings of impaired outcomes above the age of 6 contrast with earlier studies that suggested that outcomes of MLPTI are comparable to those of full-term children. However, since the number of studies performed on MLPTI above 6 years of age is limited and show different results, the developmental outcomes of MLPTI remains a subject of debate and more research to this subject is warranted.

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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Preterm Birth Developmental Delay Growth Delay

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Outcomes of a group of preterm born children are compared to a group of children born at term.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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MLPTI Cohort

Group of 9 year old children born between 32 and 36 weeks of gestational age

Group Type EXPERIMENTAL

CBCL

Intervention Type DIAGNOSTIC_TEST

A questionnaire on behaviour

SDQ

Intervention Type DIAGNOSTIC_TEST

A questionnaire on behaviour

CCC-2-NL

Intervention Type DIAGNOSTIC_TEST

A questionnaire on communcational skills

MCH Feeding scale

Intervention Type DIAGNOSTIC_TEST

A questionnaire on feeding problems

TRF

Intervention Type DIAGNOSTIC_TEST

A questionnaire on behaviour

WISC-5-NL

Intervention Type DIAGNOSTIC_TEST

An IQ test for children

Movement ABC

Intervention Type DIAGNOSTIC_TEST

A test to assess motor function

CELF-5-NL

Intervention Type DIAGNOSTIC_TEST

A test to assess language development

Emma Toolbox

Intervention Type DIAGNOSTIC_TEST

Test of executive functions

Control cohort

Group of 9 year old children born at term

Group Type ACTIVE_COMPARATOR

CBCL

Intervention Type DIAGNOSTIC_TEST

A questionnaire on behaviour

SDQ

Intervention Type DIAGNOSTIC_TEST

A questionnaire on behaviour

CCC-2-NL

Intervention Type DIAGNOSTIC_TEST

A questionnaire on communcational skills

MCH Feeding scale

Intervention Type DIAGNOSTIC_TEST

A questionnaire on feeding problems

TRF

Intervention Type DIAGNOSTIC_TEST

A questionnaire on behaviour

WISC-5-NL

Intervention Type DIAGNOSTIC_TEST

An IQ test for children

Movement ABC

Intervention Type DIAGNOSTIC_TEST

A test to assess motor function

CELF-5-NL

Intervention Type DIAGNOSTIC_TEST

A test to assess language development

Emma Toolbox

Intervention Type DIAGNOSTIC_TEST

Test of executive functions

Interventions

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CBCL

A questionnaire on behaviour

Intervention Type DIAGNOSTIC_TEST

SDQ

A questionnaire on behaviour

Intervention Type DIAGNOSTIC_TEST

CCC-2-NL

A questionnaire on communcational skills

Intervention Type DIAGNOSTIC_TEST

MCH Feeding scale

A questionnaire on feeding problems

Intervention Type DIAGNOSTIC_TEST

TRF

A questionnaire on behaviour

Intervention Type DIAGNOSTIC_TEST

WISC-5-NL

An IQ test for children

Intervention Type DIAGNOSTIC_TEST

Movement ABC

A test to assess motor function

Intervention Type DIAGNOSTIC_TEST

CELF-5-NL

A test to assess language development

Intervention Type DIAGNOSTIC_TEST

Emma Toolbox

Test of executive functions

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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Child Behaviour Checklist Strength and Difficulties Questionnaire Children's Communication Checklist Montreal Children's Hospital Feeding Scale Teacher report form Wechsler Intelligence Scale of Development for Children MABC-II-NL Clinical Evaluation of Language Fundamentals

Eligibility Criteria

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Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all the following 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

A potential subject who meets any of the following criteria will be excluded from participation in this study:

* 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
Minimum Eligible Age

9 Years

Maximum Eligible Age

9 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Noordwest Ziekenhuisgroep

OTHER

Sponsor Role lead

Responsible Party

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F. (Femke) de Groof

Principal Investigator, MD, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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Netherlands

Other Identifiers

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NL82197.029.22

Identifier Type: -

Identifier Source: org_study_id

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