Mother-infant Bonding During COVID-19

October 11, 2022 updated by: Columbia University

Promoting Mother-Infant Emotional Connection During the COVID-19 Pandemic: an Randomized Controlled Trial (RCT) of Virtual Family Nurture Intervention

The purpose of this study is to compare the mother-infant emotional connection formed during the pandemic in standard care (SC) versus Family Nurture Intervention (FNI) pairs, an evidence-based intervention designed to counteract the adverse effects of maternal-infant disconnection. In prior research on preterm infants in the neonatal intensive care unit (NICU), FNI participants demonstrated increased quality of maternal caregiving behaviors and significant improvements in premature infants' neurodevelopment across multiple domains, including social-relatedness and attention problems. Goals of FNI include assisting mothers in providing appropriate types of stimulation for their babies that are important for social, emotional, and neurobehavioral development as well as reducing stress physiology in both mother and infant. Data gathered in this study will help the investigators learn more about the underlying mechanisms that take place during mother-infant interactions and examine how these play a role in setting the infant up for the best neurodevelopmental trajectory. Intervention will be conducted electronically both in the Well Baby Nursery (WBN) and at home over the following 4 months. Assessments will consist of videos of mother-infant interactions at the time of each intervention session, and pediatrician-led follow-up surveys conducted in the linked Institutional Review Board-approved study.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Mother-infant interactions, which are well-established to strongly influence long-term neurodevelopmental outcomes, are at particular risk during the pandemic, both due to maternal stress, as well as to changes in health care policies leading to decreased interaction with healthcare providers during the immediate postpartum period. In order to minimize risk of severe acute respiratory syndrome (SARS)-CoV-2 transmission, nurses and physicians in the WBN have minimized entry and exit into patient rooms, and new moms are discharged on average one day early. In addition to psychological stress, there are also currently unknown risks to the neonates born to mothers with SARS-CoV-2 infections at various points in their pregnancy. Although viral transmission itself seems unlikely, it is currently completely unknown if secondary effects will be observed. In the case of maternal HIV infection, it is now well established that even when vertical transmission does not occur, there are negative consequences to neurodevelopmental outcomes of these exposed children. It is therefore imperative to develop preventative strategies that protect newborns and set them on the path of optimal neurodevelopment. As mother-infant nurturing interactions are known to be the most crucial ingredient in optimal neurodevelopmental trajectories, the goal of the investigators is to test the hypothesis that an intervention focused on promoting mother-infant emotional connection in the neonatal period will lead to long-term benefit and prevention of deleterious effects of the COVID-19 pandemic. The investigators will use FNI, an intervention specifically developed to enhance mother-infant emotional connection through facilitated mother-infant interactions, emotional exchanges and mutual calming sessions. Some of the facilitated interactions include: interactive touch with deep emotional expression and vocal soothing, sustained reciprocal olfactory exposure, family practice in comforting, and skin-to-skin holding. Previously at CUIMC, an RCT investigated the effects of FNI in NICU infants. Infants who received FNI showed significant increases in electroencephalogram (EEG) power, a measure of brain activity, near term age compared with those who receive Standard Care (SC). Increased EEG power has previously been shown to be associated with improved cognitive development, as measured by the Bayley Scales of Infant and Toddler Development (BSID-III). Within the group of children who scored above 85 on the Bayley-III (1 standard deviation below the mean or higher), FNI infants scored significantly higher on the BSID-III Cognitive and Language scales compared to SC infants. Additionally, FNI infants had lower risk for autism spectrum disorder (ASD) as measured by the Modified Checklist of Autism for Toddlers (M-CHAT), an early ASD screening questionnaire. FNI infants also displayed significantly lower levels of EEG coherence (1-18 Hz) largely within and between frontal regions. This finding suggests that FNI may accelerate brain maturation particularly in frontal brain regions, which are involved in regulation of attention, cognition, and emotion. Taken together, the first RCT of FNI is strongly suggestive of neurodevelopmental benefit.

Purpose/aims: The COVID-19 pandemic has made precautions necessary in the Well Baby Nursery that result in maternal stress which is known to impair mother-infant bonding, which is well-established to be critical for positive long-term neurodevelopmental and behavioral outcomes. The investigators will be conducting a randomized controlled trial (RCT) of Family Nurture Intervention (FNI) in the Morgan Stanley Children's Hospital (MSCH) Well Baby Nursery (WBN) at Columbia University Irving Medical Center (CUIMC). The RCT will compare neurodevelopmental and socio-emotional outcomes of the current standard of care (SC) during the COVID-19 pandemic with Family Nurture Intervention (FNI) conducted via telemedicine.

Study Type

Interventional

Enrollment (Anticipated)

280

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • United States
    • New York
      • New York, New York, United States, 10032
        • Recruiting
        • Morgan Stanley Children's Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 year to 1 year (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Mother agrees to participate in a linked study involving additional surveys and assessments
  • Newborn born between 37 weeks and 40 weeks and 6 days gestational age
  • Newborn is a singleton
  • Mother can speak English or Spanish

Exclusion Criteria:

  • Newborn born at less than 37 weeks and 0 days gestational age
  • Newborn born at more than 40 weeks and 6 days gestational age
  • Infant's attending physician does not recommend enrollment in the study based on newborn health concerns or diagnoses, or based on concern regarding maternal history of maternal substance abuse, severe psychiatric illness or psychosis
  • Congenital, cardiac, or chromosomal anomalies requiring special infant care beyond routine testing based on prenatal concerns (e.g. postnatal ultrasound necessary for prenatal ultrasound findings of hydronephrosis would not exclude newborn, but newborn with known Trisomy 21 would)
  • Mother and/or infant has a medical condition that precludes intervention components
  • Newborn is a twin or other multiple at birth
  • Mother is unwilling to place wearable electrophysiological recording devices on herself or her newborn
  • Mother is unwilling to be video recorded or to give consent for videos/photographs (video stills)/audio (from the videos) to be used in educational materials, scientific publications or professional meeting presentations

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Family Nurture Intervention (FNI)
Receives a FNI session over Zoom in the Well Baby Nursery and 3 subsequent Zoom sessions over the next 3 months.
Behavioral: Family Nurture Intervention (FNI)
FNI is a family based intervention that facilitates and strengthens the mother-infant emotional connection through a structured guided interaction by a Nurture Specialist. The mother is asked to sit with her baby in her arms so that they are face-to-face, and when the baby becomes restless, the physician will coach the mom to bring the baby back to a calm state. The mother will also be encouraged to verbalize her feelings to her baby. Mother-infant emotional connection is known to affect various developmental processes and improve overall health. FNI was previously shown to be efficacious in improving several long-term health outcomes in preterm infants in the neonatal intensive care unit (NICU).
No Intervention: Standard of Care (SC)
SC receives the regular standard of care in the Well Baby Nursery and no intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Welch Emotional Connection Score
Time Frame: Baseline, 1 month, 2 months, 3 months
The Welch Emotional Connection Screen (WECS) is a validated scale for quantitative assessment of the emotional connection between infant and mother by scoring the interaction of the dyad in four domains: attraction, vocal communication, facial communication, and sensitivity/reciprocity. The domains are scored on a scale from 1.0 to 3.0 in 0.25 point increments, with higher scores indicating stronger emotional connection. In combination with the rating of the four domains, the overall WECS score is classified as "emotionally connected" or "not emotionally connected." A score of "emotionally connected" or "not emotionally connected" is determined by the observers' overall assessment of the emotional connection of the dyad. The WECS will be measured at baseline for both groups, and at each of the 3 subsequent visits by a researcher observing the dyadic interaction during a 5 minute period of face-to-face time. Changes in score from baseline to 3 months will be evaluated for FNI groups.
Baseline, 1 month, 2 months, 3 months
Change in Maternal Caregiving Behavior Score (Acceptance versus Rejection)
Time Frame: Baseline, 1 month, 2 months, 3 months
The quality of caregiving in the domain of acceptance versus rejection, will be measured on a scale from 1-9, with 9 indicating higher quality caregiving. During each Zoom call, following the mother-infant interaction video but prior to intervention for the FNI group, a recording will be obtained where mother undresses infant, changes diaper, and redresses infant. This video will be scored with an adaption of the Ainsworth System for Rating Maternal Care-Giving Behavior with measures such as sensitivity and intrusiveness.
Baseline, 1 month, 2 months, 3 months
Change in Maternal Caregiving Behavior Score (Sensitivity versus Insensitivity)
Time Frame: Baseline, 1 month, 2 months, 3 months
The quality of caregiving in the domain of sensitivity versus insensitivity, will be measured on a scale from 1-9, with 9 indicating higher quality caregiving. During each Zoom call, following the mother-infant interaction video but prior to intervention for the FNI group, a recording will be obtained where mother undresses infant, changes diaper, and redresses infant. This video will be scored with an adaption of the Ainsworth System for Rating Maternal Care-Giving Behavior with measures such as sensitivity and intrusiveness.
Baseline, 1 month, 2 months, 3 months
Change in Maternal Caregiving Behavior Score (Consideration versus Intrusiveness)
Time Frame: Baseline, 1 month, 2 months, 3 months
The quality of caregiving in the domain of consideration versus intrusiveness, will be measured on a scale from 1-9, with 9 indicating higher quality caregiving. During each Zoom call, following the mother-infant interaction video but prior to intervention for the FNI group, a recording will be obtained where mother undresses infant, changes diaper, and redresses infant. This video will be scored with an adaption of the Ainsworth System for Rating Maternal Care-Giving Behavior with measures such as sensitivity and intrusiveness.
Baseline, 1 month, 2 months, 3 months
Change in Maternal Caregiving Behavior Score (Quality of Physical Contact)
Time Frame: Baseline, 1 month, 2 months, 3 months
The quality of caregiving in the domain of quality of physical contact, will be measured on a scale from 1-9, with 9 indicating higher quality caregiving. During each Zoom call, following the mother-infant interaction video but prior to intervention for the FNI group, a recording will be obtained where mother undresses infant, changes diaper, and redresses infant. This video will be scored with an adaption of the Ainsworth System for Rating Maternal Care-Giving Behavior with measures such as sensitivity and intrusiveness.
Baseline, 1 month, 2 months, 3 months
Change in Maternal Caregiving Behavior Score (Quality of Vocal Contact)
Time Frame: Baseline, 1 month, 2 months, 3 months
The quality of caregiving in the domain of quality of vocal contact, will be measured on a scale from 1-9, with 9 indicating higher quality caregiving. During each Zoom call, following the mother-infant interaction video but prior to intervention for the FNI group, a recording will be obtained where mother undresses infant, changes diaper, and redresses infant. This video will be scored with an adaption of the Ainsworth System for Rating Maternal Care-Giving Behavior with measures such as sensitivity and intrusiveness.
Baseline, 1 month, 2 months, 3 months
Change in Maternal Caregiving Behavior Score (Effectiveness of Response to Baby's Crying)
Time Frame: Baseline, 1 month, 2 months, 3 months
The quality of caregiving in the domain of effectiveness of response to baby's crying, will be measured on a scale from 1-9, with 9 indicating higher quality caregiving. During each Zoom call, following the mother-infant interaction video but prior to intervention for the FNI group, a recording will be obtained where mother undresses infant, changes diaper, and redresses infant. This video will be scored with an adaption of the Ainsworth System for Rating Maternal Care-Giving Behavior with measures such as sensitivity and intrusiveness.
Baseline, 1 month, 2 months, 3 months
Right and Left Frontal Mother & Infant EEG Synchrony
Time Frame: Baseline, Up to 3 days
2 Epilog devices will be put on mother and baby's foreheads for 2 lead EEG recording, left frontal and right frontal. EEG synchrony between mom and baby will be examined for change in synchrony over the course of the first intervention in the nursery.
Baseline, Up to 3 days
Heart Rate Variability (HRV)
Time Frame: Baseline, Up to 3 days
Epilog devices will be used to collect ECG from both mother and infant during the first interaction and intervention in the nursery. Change in synchrony of HRV will be examined over the course of the intervention.
Baseline, Up to 3 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Columbia University

Investigators

  • Principal Investigator: Dani Dumitriu, Columbia University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 13, 2020

Primary Completion (Anticipated)

December 1, 2023

Study Completion (Anticipated)

December 1, 2023

Study Registration Dates

First Submitted

August 19, 2020

First Submitted That Met QC Criteria

August 26, 2020

First Posted (Actual)

August 28, 2020

Study Record Updates

Last Update Posted (Actual)

October 13, 2022

Last Update Submitted That Met QC Criteria

October 11, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AAAT0140

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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