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.
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.
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.
.
- Conditions
- Preterm Birth, Developmental Delay, Growth Delay
- 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 group | Role | What they receive |
|---|---|---|
| MLPTI Cohort | Experimental | Group 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 cohort | Active comparator | Group 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.
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
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
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
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
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
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)
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
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
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
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:
- 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:
- emotional symptoms (5 items)
- conduct problems (5 items)
- hyperactivity/inattention (5 items)
- peer relationship problems (5 items)
- 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
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
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.
- First posted14 Aug 2023
- Study start11 Aug 2023
- Primary completion4 Jul 2026
- Study completion4 Jul 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Preterm BirthStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Noordwest Ziekenhuisgroep
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, F. (Femke) de Groof, Noordwest Ziekenhuisgroep
- Investigators
- METC AUMC, Study chair, Amsterdam UMC
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
Study at a glance
From the registry record, last updated by the sponsor on 1 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Neurodevelopmental Outcomes and Morbidities of Moderate and Late Preterm Children at the Age of 9 Years -The Alkmaar MLPTI Cohort Study
- ClinicalTrials.gov ID
- NCT05990582
- Acronym / sponsor ID
- NL82197.029.22
- Conditions
- Preterm Birth, Developmental Delay, Growth Delay
- Keywords
- Moderate and late preterm infants, Neurodevelopmental outcomes, Growth, Morbidities
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 153 participants (actual)
- Lead sponsor
- Noordwest ZiekenhuisgroepUniversity, hospital or other
- Study start
- 11 Aug 2023 (actual)
- Primary completion
- 4 Jul 2026 (actual)
- Study completion
- 4 Jul 2026 (actual)
- First posted
- 14 Aug 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 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.
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.
.
Study design
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Outcomes of a group of preterm born children are compared to a group of children born at term.
| Arm | Type | Receives |
|---|---|---|
| MLPTI Cohort | Experimental | 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 ToolboxGroup of 9 year old children born between 32 and 36 weeks of gestational age |
| Control cohort | Active comparator | 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 ToolboxGroup of 9 year old children born at term |
Who may qualify
- Ages
- 9 to 9 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| CBCLAlso: Child Behaviour ChecklistA questionnaire on behaviour | Diagnostic test | Control cohort, MLPTI Cohort |
| SDQAlso: Strength and Difficulties QuestionnaireA questionnaire on behaviour | Diagnostic test | Control cohort, MLPTI Cohort |
| CCC-2-NLAlso: Children's Communication ChecklistA questionnaire on communcational skills | Diagnostic test | Control cohort, MLPTI Cohort |
| MCH Feeding scaleAlso: Montreal Children's Hospital Feeding ScaleA questionnaire on feeding problems | Diagnostic test | Control cohort, MLPTI Cohort |
| TRFAlso: Teacher report formA questionnaire on behaviour | Diagnostic test | Control cohort, MLPTI Cohort |
| WISC-5-NLAlso: Wechsler Intelligence Scale of Development for ChildrenAn IQ test for children | Diagnostic test | Control cohort, MLPTI Cohort |
| Movement ABCAlso: MABC-II-NLA test to assess motor function | Diagnostic test | Control cohort, MLPTI Cohort |
| CELF-5-NLAlso: Clinical Evaluation of Language FundamentalsA test to assess language development | Diagnostic test | Control cohort, MLPTI Cohort |
| Emma ToolboxTest of executive functions | Diagnostic test | Control cohort, MLPTI Cohort |
Primary outcome
Full scale IQ
Time frame: At 9 years of age
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
M-ABC score
Time frame: At 9 years of age
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)
Executive functions on Emma-Toolbox
Time frame: At 9 years of age
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.
Prevalence of Morbidities
Time frame: At 9 years of age
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
Measurements of growth
Time frame: At 9 years of age
Length, weight, head and abdominal circumference are measured in cm. Parental height will be measured in cm.
Blood Pressure at 9 years of age
Time frame: At 9 years of age
Systolic bloodpressure in mmHg, range 5-200 Diastolic blood pressure in mmHg p-value is conducted for age.
6 secondary outcomes
Behavioural and psychosocial outcomes of the CBCL
Time frame: At 9 years of age
Speech- and language-developmental scores on CELF-5-NL
Time frame: At 9 years of age
Children's Communication List CCC-2-NL
Time frame: At 9 years of age
The Strengths and Difficulties Questionnaire (SDQ)
Time frame: At age of 9 years
Teacher Report Form (TRH)
Time frame: At 9 years of age
Montreal Childrens Hospital Feeding Scale (MCH)
Time frame: At 9 years of age
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
METC AUMC study chair
Amsterdam UMC
1 site in 1 country: see every site and its status.
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.