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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05898295
Other study ID # ID 2020-00572
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 19, 2021
Est. completion date December 31, 2024

Study information

Verified date June 2023
Source University Hospital, Geneva
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The project presented here aims to evaluate the discrimination capacity of the Observation of Sensory-Motor Behavior (OSMB) grid of the preterm infant, as well as its predictive capacity for the child's later psychomotor development. To do this, OSMB grids will be completed during dystimulant care and during stabilizing care in 65 preterm infants. In addition, an OSMB grid will also be completed during a sensorimotor assessment at 37 weeks gestational age and at 1 month corrected for prematurity in 100 preterm infants. The OCSM scores will then be compared to the Bayley III scale scores at 6 months of age corrected for prematurity.


Description:

The project presented here aims to evaluate the discrimination capacity of the Observation of Sensory-Motor Behavior (OSMB) grid of the preterm infant, as well as its predictive capacity for the child's later psychomotor development. To do this, OSMB grids will be completed during dystimulant care and during stabilizing care in 65 preterm infants. In addition, an OSMB grid will also be completed during a sensorimotor assessment at 37 weeks gestational age and at 1 month corrected for prematurity in 100 preterm infants. The OCSM scores will then be compared to the Bayley III scale scores at 6 months of age corrected for prematurity.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 3 Days to 6 Months
Eligibility Inclusion Criteria: - <37weeks - Hospitalized in Geneva Hospital NICU - At least one parent speaking french Exclusion Criteria: - No exclusion cirteria

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
No intervention: only observation of the child behavior

Locations

Country Name City State
Switzerland Hopitaux Universitaire de Genève Geneva

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessing the ability of the OSMB grid to discriminate the sensory-motor status of the preterm newborn in routine neonatal care practice Observation of the child's behavior during a disstimulating treatment and during a stabilizing treatment using the Observation of Sensory-Motor Behavior (OSMB) grid between birth and hospital discharge (up to 200days)
Primary To evaluate the predictive capacity of the child's later psychomotor development on the basis of the items from the sensorimotor assessment thanks to the OCSM grid, at term equivalent age Evaluation of newborns' development using the Observation of Sensory-Motor Behavior (OSMB) grid between 37 and 40weeks of gestational age
Primary To evaluate the predictive capacity of the child's later psychomotor development on the basis of the items from the sensorimotor assessment thanks to the OCSM grid, at term equivalent age Evaluation of newborns' development using the Observation of Sensory-Motor Behavior (OSMB) grid and 1 month of corrected age
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