Nurturing and Quiet Intervention: NeuroN-QI
NeuroN-QI
1 other identifier
interventional
24
1 country
1
Brief Summary
The current state of knowledge reveals that the development of the brain of preterm infants is influenced by specific neonatal experiences during hospitalization, such as environmental sensory stimulation (light and noise), as well as physical and emotional proximity to mothers. However, there is a lack of evidence regarding the benefits that could be associated with the combination of care interventions to improve the health outcomes of preterm infants and their mothers, and in particular the development of the brain of infants during their hospitalization in the neonatal unit. The aim of this pilot study is to assess the feasibility and acceptability of a developmental care intervention including periods of nurturing between mothers and their infant (skin-to-skin contact and auditory stimulation) to promote physical and emotional proximity and a quiet period (controlled light and noise levels and olfactory stimulation in incubators) and to estimate the effect of this intervention on infants' neurodevelopment as well as on maternal stress and anxiety.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2021
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 25, 2020
CompletedFirst Posted
Study publicly available on registry
October 19, 2020
CompletedStudy Start
First participant enrolled
June 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2024
CompletedMarch 20, 2025
November 1, 2023
3 years
August 25, 2020
March 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Feasibility and acceptability of the NeuroN-QI and the study procedures as assessed by a self-completed questionnaire (mothers) and a logbook (RA)
questionnaire completed by mothers - each question treated separately (no total score) Log book completed by a research assistant
1 year
Secondary Outcomes (7)
Estimated effects of NeuroN-QI on infants' neurodevelopment as assessed using the Assessment of Preterm Infants Behavior (APIB)
1 year
Estimated effects of NeuroN-QI on infants' neurodevelopment as assessed using the General Movements Assessment (GMA)
1 year
Estimated effects of NeuroN-QI on maternal stress as assessed by PSS:NICU
1 year
Estimated effects of NeuroN-QI on maternal anxiety as assessed by STAI-Y
1 year
Nurses' training needs about the NeuroN-QI as assessed by a self-completed questionnaire
1 year
- +2 more secondary outcomes
Other Outcomes (1)
Confounding variables
1 year
Study Arms (2)
Experimental
EXPERIMENTALEach SSC session will last 2-hr during the day including a 15-min of auditory stimulation with maternal voice and controlled levels of NICU light and noise. The 2-hr SSC will be followed by a 1-hr quiet period where infants will rest in their incubator/crib with a pad immersed with their mother breast milk for olfactory stimulation and where the control of light and noise levels will be continued. The NeuroN-QI will be done 4 times/wk for each dyad.
Control
NO INTERVENTIONMothers-infant dyads will do 4 SSC/wk. During these sessions, no attempt will be made by the RA to control the light and noise levels nor to encourage auditory stimulation. The SSC periods will not be followed by a quiet period nor olfactory stimulation.
Interventions
SSC session lasting 2-hr during the day 4 times/wk including a 15-min of auditory stimulation with maternal voice and controlled levels of NICU light and noise followed by a 1-hr quiet period where infants will rest in their incubator/crib with olfactory stimulation and where the control of light and noise levels will be continued.
Eligibility Criteria
You may qualify if:
- Infants:
- \- born between 26 and 316/7 WGA.
- Mothers
- agree to do 4 SSC sessions/week with a 15-minutes period of auditory (reading) stimulation;
- express breast milk for their infant;
- speak, read, or write French or English.
- Nurses:
- have at least 6 months of work experience in a NICU;
- speak and read French or English.
You may not qualify if:
- Infants:
- have birth defects or genetic disorders;
- have an intraventricular hemorrhage \> grade II;
- receive nasal respiratory support;
- have been transferred from another hospital.
- Mothers:
- are \<18 years of age;
- had a multiparous birth;
- have a physical condition that does not allow SSC;
- abuse substances or alcohol;
- do not intend to breastfeed or give breastmilk.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Sainte-Justine
Montreal, Quebec, H3T 1C5, Canada
Related Publications (1)
Aita M, Heon M, Lavallee A, De Clifford Faugere G, Altit G, Le May S, Dorval V, Lippe S, Larone Juneau A, Remmer E, Rennick JE. Nurturing and quiet intervention (NeuroN-QI) on preterm infants' neurodevelopment and maternal stress and anxiety: A pilot randomized clinical trial protocol. J Adv Nurs. 2021 Jul;77(7):3192-3203. doi: 10.1111/jan.14819. Epub 2021 Mar 14.
PMID: 33719093DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Marilyn Aita, PhD
St. Justine's Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor & Researcher
Study Record Dates
First Submitted
August 25, 2020
First Posted
October 19, 2020
Study Start
June 1, 2021
Primary Completion
June 1, 2024
Study Completion
June 1, 2024
Last Updated
March 20, 2025
Record last verified: 2023-11
Data Sharing
- IPD Sharing
- Will not share