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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06111898
Other study ID # 2023-01113
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 10, 2023
Est. completion date December 31, 2027

Study information

Verified date November 2023
Source University Hospital, Geneva
Contact Nathalie De Beukelaer, PhD
Phone +41783033552
Email nathalie.debeukelaer@unige.ch
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This project focuses on motor development, muscle growth and muscle activity. Using advanced, instrumented tests such as , the link between muscles and the movement characteristics will be studied. In addition, the evolution of these neuro-biomechanical determinants during the first year of life will be investigated. The examinations are planned for a group of high-risk infants (e.g. premature birth, cases of asphyxia, etc.) compared with a group of infants with typical development.


Description:

Background and rationale: Prematurity and the associated causes of perinatal brain damage, as well as neonatal stroke and birth asphyxia, are major risk factors for neurodevelopmental disorders appearing from birth. In addition, these neuromotor disorders resulting from impaired brain development appear progressively over the course of the first year, affecting early movement and muscle growth. Therefore, early diagnosis and motor therapy are essential to improve long-term neurodevelopmental outcomes. However, in order to provide adequate strategies for these high-risk infants, it is crucial to identify the determinants of potential neuromotor deficits and their consequences on early motor behavior and developmental trajectory during the first year of life. A multimodal tool is needed to reveal the early neuro-biomechanical determinants of motor behavior in infants at high risk of neurodevelopmental disorders. Objective(s): - Establishing a comprehensive multimodal tool for the assessment of neuro-biomechanical determinants of motor behavior in the first year of life in high-risk infants for neurodevelopmental impairments, further referred to as "advanced muscle and movement analysis (AMMA)" - Revealing early neuro-biomechanical determinants in high-risk infants covering the first year of life, including the time points in the neonatal period, at term age, at 3 months of (corrected) age, at 6 months of (corrected) age and at 12 months of (corrected) age, by using the AMMA Outcome(s): - Using valid and reliable assessments within the protocol - Differences in neuro-biomechanical determinants between typically developing infants and high-risk infants at each time point. - Associations between the neuro-biomechanical determinants of motor behaviour in high-risk infants at each time point - Changes over time and interaction in the neuro-biomechanical determinants, and comparisons of these evolutions in high-risk infants with typical development. Methodology The current study is a national, single center (Geneva University Hospitals), observational study. This observational research will perform both cross-sectional and longitudinal data collection for cohorts of live-born infants. The study population for this study will include children, i.e., neonates and infants between the age of 35-36 weeks of gestational age to 12 months of (corrected) age. Further, two main groups of children will be included, (a) typically developing (TD) children and (b) children at high-risk for neurodevelopmental impairments. The TD children will be used as a control group. Procedure Multiple study visits are planned for longitudinal data collection within the first year of life, i.e. a time of term age, at 3 months, at 6 months and 12 months of age. For the preterms, the investigators also plan to perform an assessment in the neonatal period, i.e. 35-36 weeks of gestation. The duration of each visit session will be around 90 minutes per participant, providing also time for feeding moments and adaptation of the infant to the new environment. The visit in the neonatal period will be organized at the Neonatology Unit at HUG (Geneva University Hospitals). All visits from the term (equivalent) age will be organized in the Kinesiology Laboratory at the HUG. In general, clinical data such as birth information, structural brain MRI and developmental assessments will be derived from the medical records. The main procedures during each research visit are: 1. Muscle assessment: using 3D freehand ultrasound technique, measuring the lower legs muscles, assessing muscle volume and length. 2. Neuromotor development: using standardized scales, measuring the gross motor development and motor repertoire, assessing age-appropriate neuromotor development. 3. Motor behavior: using surface electromyography and motion capture system, measuring spontaneous movements, assessing the movement quality and quantity


Recruitment information / eligibility

Status Recruiting
Enrollment 348
Est. completion date December 31, 2027
Est. primary completion date March 31, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 35 Weeks to 1 Year
Eligibility Inclusion & exclusion criteria for group of high-risk infants: - Infants born before or at 28 weeks of gestation - Infants born after 28 weeks of gestation and with brain injury. - A term birth with the clinical diagnosis of asphyxia (ischemic event with hypothermia) or neonatal stroke - Exclusion in case of genetic syndrome, or lower limb pathology (e.g. spina bifida) Inclusion & exclusion criteria for group of typically developing children: - Born at a gestational age above 37 weeks - Birth weight between P10 and P90 - Head circumference between P10 and P90 - Ph >7.1 - Exclusion in case of genetic syndrome, lower limb pathology and/or brain malformations

Study Design


Intervention

Other:
No Intervention
No intervention

Locations

Country Name City State
Switzerland University Hospitals Geneva Geneva

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

References & Publications (5)

De Beukelaer N, Vandekerckhove I, Huyghe E, Molenberghs G, Peeters N, Hanssen B, Ortibus E, Van Campenhout A, Desloovere K. Morphological Medial Gastrocnemius Muscle Growth in Ambulant Children with Spastic Cerebral Palsy: A Prospective Longitudinal Study. J Clin Med. 2023 Feb 16;12(4):1564. doi: 10.3390/jcm12041564. — View Citation

Gough M, Shortland AP. Could muscle deformity in children with spastic cerebral palsy be related to an impairment of muscle growth and altered adaptation? Dev Med Child Neurol. 2012 Jun;54(6):495-9. doi: 10.1111/j.1469-8749.2012.04229.x. Epub 2012 Feb 27. — View Citation

Pascal A, Govaert P, Oostra A, Naulaers G, Ortibus E, Van den Broeck C. Neurodevelopmental outcome in very preterm and very-low-birthweight infants born over the past decade: a meta-analytic review. Dev Med Child Neurol. 2018 Apr;60(4):342-355. doi: 10.1111/dmcn.13675. Epub 2018 Jan 19. — View Citation

Rosenbaum P, Paneth N, Leviton A, Goldstein M, Bax M, Damiano D, Dan B, Jacobsson B. A report: the definition and classification of cerebral palsy April 2006. Dev Med Child Neurol Suppl. 2007 Feb;109:8-14. Erratum In: Dev Med Child Neurol. 2007 Jun;49(6):480. — View Citation

Willerslev-Olsen M, Choe Lund M, Lorentzen J, Barber L, Kofoed-Hansen M, Nielsen JB. Impaired muscle growth precedes development of increased stiffness of the triceps surae musculotendinous unit in children with cerebral palsy. Dev Med Child Neurol. 2018 Jul;60(7):672-679. doi: 10.1111/dmcn.13729. Epub 2018 Mar 24. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary General Movement Assessment Observation of general movements following the Prechtl's General Movement Assessment, interpreted by observing age-specific general movement components and extracting the Motor Optimality Score (0-12, the higher, the better outcome) 35-36 weeks of gestation; term equivalent age, 3 months (corrected) age
Primary Hammersmith Neonatal/Infant Neurological Examination Neurological assessment for different domains such as muscle tone, postures, movements and reflexes . Resulting in total scores (0-78) which can be compared to norm values, and higher scores indicate better outcome. 35-36 weeks of gestation; term equivalent age, 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Primary Change in muscle morphology size The size of the lower leg muscles defined by freehand ultrasound 35-36 weeks of gestation; term equivalent age, 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Primary Change in muscle morphology length The length of the lower leg muscles defined by freehand ultrasound 35-36 weeks of gestation; term equivalent age, 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Primary Change in muscle activity Investigation of the muscle activity during spontaneous, whole body movements by using surface electromyography. 35-36 weeks of gestation; term equivalent age, 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Primary Change in motor behaviour Investigation movement quality/quantify during spontaneous, whole body movements by using reflective markers. 35-36 weeks of gestation; term equivalent age, 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Secondary Bayley Scales of Infant and Toddler Development - Version III Standardized neurodevelopmental test of gross and fine motor skills. Higher scores indicate better outcome. 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Secondary Alberta Infant Motor Scale (AIMS) Assessment of gross motor development during prone, supine, sitting and standing. Scores from 0-60. Higher scores indicate better outcome. 3 months (corrected) age, 6 months (corrected) age and 12 months (corrected) age.
Secondary Magnetic resonance imaging of the brain: classification Qualitatively assessment on the MRI classification system by Himmelman et al. to classify the nature of brain abnormalities. up to 4 weeks post-term age
Secondary Magnetic resonance imaging of the brain: quantification Qualitatively assessment on the MRI classification system by quantitative assessment using the Kidokoro scoring system to classify the extent of white and grey matter abnormalities. Total global scores were classified as normal (0-3), mild (4-7), moderate (8-11), or severe (=12) brain abnormalities. up to 4 weeks post-term age
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