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Preterm BirthNCT05990582

The Alkmaar MLPTI Cohort Study: Outcomes at 9 Years

A study testing CBCL, SDQ and CCC-2-NL in people with Preterm Birth and Developmental Delay, run by Noordwest Ziekenhuisgroep at 1 site in Netherlands.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 9 to 9 yearsHealthy volunteers can take part
Conditions the study is for
Preterm Birth, Developmental Delay, Growth Delay
What is being tested?
CBCL, SDQ and CCC-2-NL
Could I receive a placebo?
No, everyone receives an active treatment
How many people
153 participants
Where
1 siteNetherlands
Study dates
11 Aug 2023to 4 Jul 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 9 to 9 years
  • All sexes
  • Healthy volunteers accepted
  • Child

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 or has visited a GGD site for the 9 years vaccination and is willing to participate or is a (grand)child of an employee of Noordwest Hospital and is living in the area of Alkmaar (< 20 km).
  • Both parents of the participant have given informed consent for the participation of the study.

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

Trial locations and contacts

1 site in 1 country.

Netherlands1 site
  • Noordwest Ziekenhuisgroep

    Alkmaar, 1815JD

Other trials in Netherlands

About this study

Official title: Neurodevelopmental Outcomes and Morbidities of Moderate and Late Preterm Children at the Age of 9 Years -The Alkmaar MLPTI Cohort Study

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.

Read more

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 and also 9 year old children who are living in the area of Alkmaar (< 20 km) and who are invited by the GGD to receive vaccinations at the age of 9 years old or 9 year old children of employees of Noordwest Hospital and all born at full term. (n=70).

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.

Read the detailed description

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 or 9 year old children who are living in the area of Alkmaar (< 20 km) and who are invited by the GGD to receive vaccinations at the age of 9 or 9 year old children of employees of Noordwest Hospital and all born at full term.

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 or 9 year old children who are living in the area of Alkmaar (< 20 km) and who are invited by the GGD to receive vaccinations at the age of 9 years old and 9 year old children of employees of Noordwest Hospital and all born at full term 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 or 9 year old children who are living in the area of Alkmaar (< 20 km) and who are invited by the GGD to receive vaccinations at the age of 9 years old and 9 year old children of employees of Noordwest Hospital and all 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.

.

Being tested
CBCL, SDQ, CCC-2-NL, MCH Feeding scale, TRF
Keywords
Moderate and late preterm infants, Neurodevelopmental outcomes, Growth, Morbidities
Medical subject headings
Premature Birth, Learning Disabilities, Lymphoma, Follicular

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CBCLDiagnostic test

    Also called Child Behaviour Checklist

    A questionnaire on behaviour

  • SDQDiagnostic test

    Also called Strength and Difficulties Questionnaire

    A questionnaire on behaviour

  • CCC-2-NLDiagnostic test

    Also called Children's Communication Checklist

    A questionnaire on communcational skills

  • MCH Feeding scaleDiagnostic test

    Also called Montreal Children's Hospital Feeding Scale

    A questionnaire on feeding problems

  • TRFDiagnostic test

    Also called Teacher report form

    A questionnaire on behaviour

  • WISC-5-NLDiagnostic test

    Also called Wechsler Intelligence Scale of Development for Children

    An IQ test for children

  • Movement ABCDiagnostic test

    Also called MABC-II-NL

    A test to assess motor function

  • CELF-5-NLDiagnostic test

    Also called Clinical Evaluation of Language Fundamentals

    A test to assess language development

  • Emma ToolboxDiagnostic test

    Test of executive functions

Study groups in NCT05990582
Study groupRoleWhat they receive
MLPTI CohortExperimentalGroup of 9 year old children born between 32 and 36 weeks of gestational age
Receives: Diagnostic Test: CBCL; Diagnostic Test: SDQ; Diagnostic Test: CCC-2-NL; Diagnostic Test: MCH Feeding scale; Diagnostic Test: TRF; Diagnostic Test: WISC-5-NL; Diagnostic Test: Movement ABC; Diagnostic Test: CELF-5-NL; Diagnostic Test: Emma Toolbox
Control cohortActive comparatorGroup of 9 year old children born at term
Receives: Diagnostic Test: CBCL; Diagnostic Test: SDQ; Diagnostic Test: CCC-2-NL; Diagnostic Test: MCH Feeding scale; Diagnostic Test: TRF; Diagnostic Test: WISC-5-NL; Diagnostic Test: Movement ABC; Diagnostic Test: CELF-5-NL; Diagnostic Test: Emma Toolbox

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Full scale IQ

    The primary index scores and the FSIQ are on a standard score metric with a mean of 100 and an SD of 15. The primary index scores range from 45 to 155; the FSIQ ranges from 40 to 160.

    For both the primary index scores and the FSIQ, scores ranging from 90 to 109 are typically considered average

    Measured: At 9 years of age

  2. M-ABC score

    Standard Score: Total and percentile Total score 0, percentile 96-100 (high) Totalscore 4, percentile 54 (moderate) Totalscore 10, percentile 15 (consider help/intervention) totalscore 13,5, percentile 5 (intervention needed)

    Measured: At 9 years of age

  3. Executive functions on Emma-Toolbox

    Processing speed \& Control Verbal Memory Visual memory Verbal working Memory Visual Working Memory Interpretation: Cortex. 2021 Oct;143:12-28. doi: 10.1016/j.cortex.2021.06.011. Epub 2021 Jul 14 Visuomotoric integration.

    Measured: At 9 years of age

  4. Prevalence of Morbidities

    This questionary scores the following morbities in percentages (numbers of participants with): re-admission in hospital, amount of infections, eczema, astma, speech and developmental problems, medication use, operations

    Measured: At 9 years of age

  5. Measurements of growth

    Length, weight, head and abdominal circumference are measured in cm. Parental height will be measured in cm.

    Measured: At 9 years of age

  6. Blood Pressure at 9 years of age

    Systolic bloodpressure in mmHg, range 5-200 Diastolic blood pressure in mmHg p-value is conducted for age.

    Measured: At 9 years of age

Secondary outcomes (6)
  1. Behavioural and psychosocial outcomes of the CBCL

    Each item is scored using the scale: 0 = not true (as far as you know); 1 = somewhat or sometimes true; 2 = very true or often true. A total score of total behavorial problems is calculated and divided ingeTotal Score of behaviorial problems divided in internlizing behavorial problems and external behaviorial problems. A total T- score above 50 indicates that there are more problems than de controlgroup. the higher the score the more problems.

    Measured: At 9 years of age

  2. Speech- and language-developmental scores on CELF-5-NL

    Standard Score: This scores are derived from the total raw scores for each test and are on a normalized score scale that has a mean of 10 and a standard deviation (SD) of 3. A scaled score of 10 describes the average of a given age group. Scores of 7 and 13 are 1 SD below and above the mean, respectively The Children's Communication Checklist-2 U.S. Edition is a parent or caregiver rating scale based on the extensive research of author, Dr. Dorothy Bishop. CCC-2 helps rate aspects of communication, screens for general language, and identifies pragmatic language impairment. Domains that are tested is language: speech, syntax, sematics and coherence and pragmatics in scores.

    These scores are derived from the total raw scores for each test and are on a normalized score scale that has a mean of 10 and a standard deviation (SD) of 3 of 10 describes the average of a given age group. Scores of 7 and 13 are 1 SD below and above the mean, respectively

    Measured: At 9 years of age

  3. Children's Communication List CCC-2-NL

    The Children's Communication Checklist-2 U.S. Edition is a parent or caregiver rating scale based on the extensive research of author, Dr. Dorothy Bishop. CCC-2 helps rate aspects of communication, screens for general language, and identifies pragmatic language impairment. Domains that are tested is language: speech, syntax, sematics and coherence and pragmatics in scores.

    These scores are derived from the total raw scores for each test and are on a normalized score scale that has a mean of 10 and a standard deviation (SD) of 3 of 10 describes the average of a given age group. Scores of 7 and 13 are 1 SD below and above the mean, respectively

    Measured: At 9 years of age

  4. The Strengths and Difficulties Questionnaire (SDQ)

    The SDQ is a brief behavioural screening questionnaire about 2-17 year olds. It includes between one and three of the following components:

    1. 25 items on psychological attributes.

    All versions of the SDQ ask about 25 attributes, some positive and others negative. These 25 items are divided between 5 scales:

    1. emotional symptoms (5 items)
    2. conduct problems (5 items)
    3. hyperactivity/inattention (5 items)
    4. peer relationship problems (5 items)
    5. prosocial behaviour (5 items) A total score kan be calculated. A the T-score < 80 is considered as normal, 80-90 might indicate small problems,, a score > 90 indicates serious problems.

    Measured: At age of 9 years

  5. Teacher Report Form (TRH)

    This is the CBCL test filled in by the teacher. Each item is scored using the scale: 0 = not true (as far as you know); 1 = somewhat or sometimes true; 2 = very true or often true. A total score of total behavorial problems is calculated and divided ingeTotal Score of behaviorial problems divided in internlizing behavorial problems and external behaviorial problems. A total T- score above 50 indicates that there are more problems than de controlgroup. the higher the score the more problems.

    Measured: At 9 years of age

  6. Montreal Childrens Hospital Feeding Scale (MCH)

    The Montreal Children's Hospital Feeding Scale [MCH-Feeding Scale]) designed to identify feeding problems in children.

    Normal range = raw score 0-45 [T-score 35-60], mild difficulties = 46-52 [T-score 61-65], moderate 53-58 [T-score 66-70], severe >=59 [T-score >70].

    Measured: At 9 years of age

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Aug 2023
  2. Study start11 Aug 2023
  3. Primary completion4 Jul 2026
  4. Study completion4 Jul 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
Outcomes of a group of preterm born children are compared to a group of children born at term.
Masking
None (open label)
Enrolment
153 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05990582
Sponsor's protocol ID
NL82197.029.22
Status last verified
Aug 2026
First submitted
25 Jul 2023
Last updated
1 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing CBCL, SDQ and CCC-2-NL in people with Preterm Birth and Developmental Delay, run by Noordwest Ziekenhuisgroep at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Full scale IQ (time frame: At 9 years of age). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Sep 2026.

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