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ID
Source
Brief title
Health condition
The project studies the general population to create norms. IMP and SINDA are used to detect at early age children with developmental disorders such as cerebral palsy.
Het huidige onderzoek betreft de verzameling van normgegevens in de algemene populatie. IMP en SINDA richten zich op de vroegdectectie van ontwikkelingsstoornissen zoals cerebrale parese ('spasticiteit')
Sponsors and support
Stichting Ontwikkelingsneurofysiologie Groningen
Intervention
Outcome measures
Primary outcome
Infant Motor Profile Total Score
Secondary outcome
Infant Motor Profile Domain scores, i.e., score of Variation, Adaptatility, Symmetry, Fluency and Performance
SINDA neuromotor score
SINDA developmental score
Background summary
Recently two neurodevelopmental assessments have been developed: the Infant Motor Profile (IMP) and the Standardized Infant NeuroDevelopmental Assessment (SINDA). The IMP assesses infant motor behaviour and assists in high risk infants tailor-made physical therapy guidance and prediction of developmental outcome. SINDA assists general paediatricians to detect at early age infants at risk for neurodevelopmental disorders.
Objective: To obtain norm data for IMP and SINDA
Study design: Cross-sectional study
Study population: Representative sample of the general population of infants, 2–18 months (n=1700; 100 per month)
Main study parameters/endpoints: IMP scores and SINDA scores
Study objective
descriptive study: data collection for norms of two novel infant assessments, i.e., the Infant Motor Profile (IMP) and the Standardized Infant NeuroDevelopmental Assessment (SINDA)
Study design
Infants are assessed once.
Intervention
none
P.O. Box 30.001
M. Hadders-Algra
Hanzeplein 1
Groningen 9700 RB
The Netherlands
+31 (0)50 3614252
m.hadders-algra@med.umcg.nl
P.O. Box 30.001
M. Hadders-Algra
Hanzeplein 1
Groningen 9700 RB
The Netherlands
+31 (0)50 3614252
m.hadders-algra@med.umcg.nl
Inclusion criteria
The child lives in one of the three northern provinces of The Netherlands
Age at inclusion between 2 and 18 months
Parents or legal representatives will provide written informed consent
Exclusion criteria
Severe illness precluding the assessment, such as complex congenital heart disorders with insufficient oxygen saturation
Parents have insufficient understanding of the Dutch or English language to be able to give informed consent
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL6039 |
| NTR-old | NTR6170 |
| Other | NL 58069.042.16 : METc 2016/294 |