Norwalk Feasibility Study

Sponsor
Columbia University (Other)
Overall Status
Completed
CT.gov ID
NCT04048720
Collaborator
Norwalk Housing Authority (NHA) (Other)
38
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1
2.9
13.1

Study Details

Study Description

Brief Summary

The purpose of this study is two-fold: 1) to examine the feasibility of the Drop-In model of Family Nurture Intervention (FNI); and 2) to collect pilot data concerning the mother's response to the Drop-In model of FNI and short term effects of participation. Feasibility of the Program will be measured through costs, staffing, space availability, and uptake. Participation in the Drop-In entails weekly visits for FNI. The investigators hypothesize that the Family Nurture Intervention will show feasibility through attendance and positive response to the Drop-In format. The investigators also expect the Family Nurture Intervention to improve mother's perceived well-being and mother-child emotional connection.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Family Nurture Intervention
N/A

Detailed Description

Family Nurture Intervention (FNI) is a novel family-based program that facilitates mother-child emotional connection and co-regulation. Many current interventions aim at helping the child to self-regulate with or without the mother's help. However, the ability of the mother-child dyad to promote optimal development is dependent on their ability to co-regulate. The interactive co-regulation between the mother and the child shapes the behavior of both the mother and the child.

This study aims to investigate the feasibility and short term effects of participation in the Family Nurture Intervention for preschool aged children with developmental and behavior problems. Mothers and children will be engaged by Nurture Specialists in comforting and calming interactions to co-regulate with each other during weekly group sessions with the support of study staff. Intervention sessions will occur over the course of eight weeks, and each mother will decide how many sessions to attend.

Study Design

Study Type:
Interventional
Actual Enrollment :
38 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Norwalk Drop-In Family Nurture Intervention
Actual Study Start Date :
Jul 5, 2019
Actual Primary Completion Date :
Oct 1, 2019
Actual Study Completion Date :
Oct 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Family Nurture Intervention (FNI)

FNI sessions will be held once a week in the afternoon for eight weeks. Participants will take part in FNI group therapy with their child alongside other mother-child pairs. One to two staff members will lead FNI sessions.

Behavioral: Family Nurture Intervention
The mother-child pair will be asked to talk and play with each other as the pair customarily does. If the child becomes restless and dysregulated, the mother will be coached by the Nurture Specialist to bring the child back into a calm state through sustained physical contact, comforting touch, soothing words and eye contact. Each dyad will be offered eight group FNI sessions.
Other Names:
  • FNI
  • Outcome Measures

    Primary Outcome Measures

    1. Mother-child session interest [8 weeks]

      Study staff will track interest level and engagement with FNI through weekly forms and notes; mothers will be asked to give feedback on their experience of the study at the completion of eight weeks.

    2. Change in videotaped Welch Lap Test [8 weeks]

      Mother-child 5-minute videotaped interactions, recorded weekly after each session, will be assessed for social engagement and emotional connection via the Welch Emotional Connection Screen (WECS). The Welch Emotional Connection Scale (WECS) construct is emotional connection between mother and child, which the investigators hypothesize predicts optimal development. There are four items on the WECS: Mutual Attraction, Mutual Vocal Exchange, Mutual Facial Engagement, and Mutual Sensitivity/Reciprocity. Each item is rated on a scale from 1 to 3 in 0.25 increments with a score of 3 considered optimal. There is also a binary question to the rater asking if the pair is emotionally connected - yes or no. The mother and child are scored as a pair, not individually.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    24 Months to 78 Months
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Mother is fluent in English or Spanish

    • Mother is 18 years of age or older at the time of consent

    • Mother-child pair does not demonstrate emotional connection as measured by the WECS

    • Child is between the ages of 2 to 4½ years at date of enrollment (child must be younger than 4 years and 9 months at baseline assessment) or between 2 to 4½ at date of enrollment in study AAAQ9547

    • Child resides with mother

    Exclusion Criteria:
    • The child has severe congenital anomalies or chromosomal anomalies including Downs syndrome and Cerebral Palsy

    • The child has a diagnosis of Autism Spectrum Disorder

    • The child has severe motor or physical disability

    • Mother currently presents with psychosis or is currently taking antipsychotic medication

    • Current maternal drug and/or alcohol abuse

    • Mother is more than four months pregnant

    • Mother and/or infant has a medical condition or contagion that precludes intervention components

    • Mother is unable to commit to study schedule

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Norwalk Housing Authority Norwalk Connecticut United States 06854

    Sponsors and Collaborators

    • Columbia University
    • Norwalk Housing Authority (NHA)

    Investigators

    • Principal Investigator: Martha Welch, MD, Columbia University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Columbia University
    ClinicalTrials.gov Identifier:
    NCT04048720
    Other Study ID Numbers:
    • AAAS0112
    First Posted:
    Aug 7, 2019
    Last Update Posted:
    Nov 9, 2020
    Last Verified:
    Nov 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Columbia University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 9, 2020