- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04624347
NEOVIDEO : Impact of Monitoring Motor Activity by Video Analysis on the Sleep of Very Preterm Infants
Very premature birth and the necessary hospitalization expose to a risk of morbidity and mortality which impacts the neurodevelopmental prognosis. Sleep and behavior monitoring have not been developed in the neonatal units. This has to be improved since it is known from clinical and animal studies that the quality, organization and quantity of sleep in very preterm infants impact neurological development and brain plasticity.
The collection system provide neonatal care nurse with access to motion curves (evaluated by signal processing of live video) and real-time infrared video (also available in low-light conditions).
This new non-invasive technology allows an evaluation of the activity cycles of the newborn by the caregivers which until now was only accessible occasionally by short recordings of actigraphy or polysomnography. The investigators wish to demonstrate that this can contribute to an organization of care that respects the sleep patterns of the newborn, which they know to condition the neurodevelopmental prognosis.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Brest, France, 29200
- Pôle Femme Mère Enfant
-
-
Bretagne
-
Rennes, Bretagne, France, 35000
- CHU Rennes Hôpital Sud
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
New born :
- hospitalized in neonatology,
- at least one of whose legal representatives has given free, informed and written consent,
- term of birth <32 WA, postnatal age> 15 days and post-conceptual age between [30-38] WA,
- affiliated to a social security scheme
Caregivers:
- having at least 1 year of practical experience in neonatology,
- having been trained in the clinical basics of evaluating newborn sleep,
- having given their consent to participate.
Exclusion Criteria:
New born :
- sedative or curare treatment (opiates, benzodiazepines, curare, barbiturates) in the last 24 hours,
- chromosomal abnormalities identified
- Planned discharge date incompatible with the completion of the entire study
No criteria for caregivers
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Acess to Videos and Movement curves
with caregivers' access to videos and movement curves (4 days)
|
intervention of caregivers with access to videos and motion curves of the premature infant
|
|
No Intervention: No Acess to Video and Movement curves
without caregivers' access to videos and movement (4 days)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantification of the percentage of time spent in sleep
Time Frame: for 8 days
|
Quantification of the percentage of time spent in sleep (stage 1 + 2 of the neurobehavioral classification of Prechtl in 5 stages compared to the total duration of the analyzable tracing) by a supervised expert, viewing the blinded sequences of the condition tested (with and without access caregivers to video and movement curves).
|
for 8 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantification of the ratio of time spent in calm sleep / time spent in restless sleep .
Time Frame: for 8 days
|
Prechtl stage 1 / stage 2 ratio
|
for 8 days
|
|
- Quantification of the percentage of time spent in the 5 stages of Prechtl / total analyzable tracing time.
Time Frame: for 8 days
|
for 8 days
|
|
|
- Quantification of sleep fragmentation and the different types of transitions: number and duration of awakening periods
Time Frame: for 8 days
|
for 8 days
|
|
|
- Quantification of sleep fragmentation and the different types of transitions: number and duration of movement periods (periods defined by successions of movements spaced less than 5 seconds apart)
Time Frame: for 8 days
|
movement periods = periods defined by successions of movements spaced less than 5 seconds apart
|
for 8 days
|
|
- Quantification of sleep fragmentation and the different types of transitions: classification of all transitions between stages
Time Frame: for 8 days
|
for 8 days
|
|
|
- Care interventions: Quantification of the number and estimated stage of sleep at their initiation (in the 2 minutes preceding the intervention)
Time Frame: for 8 days
|
for 8 days
|
|
|
- Care interventions: Quantification of the duration and estimated stage of sleep at their initiation (in the 2 minutes preceding the intervention)
Time Frame: for 8 days
|
for 8 days
|
|
|
- Care interventions: Quantification of the type (noise or manual intervention) and estimated stage of sleep at their initiation (in the 2 minutes preceding the intervention)
Time Frame: for 8 days
|
for 8 days
|
|
|
- Textual analysis (lexical field) of the interview with the parents on their feelings about the device
Time Frame: At the end of 8 days recordings
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At the end of 8 days recordings
|
|
|
- Textual analysis (lexical field) of the interview with the nursery nurses on their feelings about the device
Time Frame: At the end of 8 days recordings
|
At the end of 8 days recordings
|
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- Analysis of the score of the "Ages and Stages questionnaires / Second Edition" sent to parents before their child's 24-month visit.
Time Frame: at 24 months
|
Evaluate the child's skills in the various areas of his development. Questionnaire with 5 sections (Communication, Gross motor skills,Fine motor skills,Problem solving, Individual or social skills). Results sheet allowing rapid interpretation (positivity threshold for each sphere) and recommendations for each developmental area screened. |
at 24 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Céline CITTE, pediatric nurse, University Hospital of Rennes
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 35RC18_8855_NEOVIDEO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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