search
Back to results

Nutrition Recommendation Intervention trialS in Children's Healthcare (NuRISH)

Primary Purpose

Obesity, Childhood, Nutrition, Health Risk Behaviors

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Childcare Navigator
Lactation Consultant
Lactation Consultant Support and Childcare Navigator Support
Control Group
Sponsored by
The Hospital for Sick Children
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity, Childhood focused on measuring Lower adiposity, Higher breastfeeding self-efficacy, Higher centre-based childcare attendance, Improved child development and mental health, Lower cardiovascular risk factors, Better dietary quality, Lower healthcare and overall societal costs

Eligibility Criteria

1 Day - 1 Week (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy by parental report
  • <32 weeks gestation
  • 0-1 week of age
  • First birth /first time parents
  • Family income <$70,000

Exclusion Criteria:

  • Children with a syndrome associated with obesity or developmental delay

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    Control Group

    Intervention Group

    Arm Description

    Participants who are randomized to the control group will receive usual care from their health care practitioners.

    Participants who are randomized to Intervention Group will receive one of three possible "scenarios": 1) Childcare Navigator Support, 2) Breastfeeding support via Lactation Consultant, 3) both Childcare Navigator Support and Breastfeeding support via Lactation.

    Outcomes

    Primary Outcome Measures

    zBMI
    The primary outcome measure will be age and sex standardized BMI z-score (zBMI), which will be measured at the 2-year primary healthcare visit. zBMI is an important outcome that is predictive of adiposity in later childhood, adolescence and adulthood. Data including birthweight and length, and repeated measures of weight and length will be used to calculate zBMI growth trajectories.

    Secondary Outcome Measures

    breastfeeding self-efficacy
    change in breastfeeding self-efficacy measured by lactation consultant logs
    exclusive breastfeeding duration
    change in exclusive breastfeeding duration
    Childcare attendance
    change in centre-based childcare attendance measured by attendance logs
    cognitive development
    To capture child's development, the Ages and Stages Questionnaire will be administered. The Ages and Stages Questionnaire identifies infants, toddlers and preschool aged children at risk of a developmental delay in five developmental domains: Communication, Gross Motor, Fine Motor, Problem Solving and Personal Social Behaviour. Each domain consists of six questions about important age-specific developmental milestones. If a child scores between 1 and 2 below the normative mean on any domain, rescreening is recommended. When a child scores 1 below the normative mean on two or more domains, or 2 below the normative mean on at least one domain, a referral to a health care professional is recommended.
    maternal mental health
    change in maternal mental health, measured by the Edinburgh Postnatal Depression Scale at 2 years of age. The scale was developed for screening postpartum women in outpatient, home visiting settings, or at the 6 -8 week postpartum examination. Consisting of 10 questions, each response is scored 0, 1, 2, or 3 according to increased severity of the symptom. Items marked with an asterisk (*) are reverse scored (i.e., 3, 2, 1, and 0). The total score is determined by adding together the scores for each of the 10 items. A woman scoring 9 or more points or indicating any suicidal ideation - that is she scores 1 or higher on question #10 - should be referred immediately for follow-up. Even if a woman scores less than 9, if the clinician feels the client is suffering from depression, an appropriate referral should be made.
    mental health
    Child's mental health captured by the Strengths and Difficulties Questionnaire. The questionnaire consists of 25 items subdivided into four difficulties scales, emotional symptoms, conduct problems, inattention-hyperactivity and peer problems, and a separate fifth strength scale, prosocial behavior. All subscales have five questions. Each item has to be scored on a 3-point scale with 0 = 'not true', 1 = 'somewhat true' and 2 = 'certainly true'. A higher score indicates more emotional and behavioral problems.
    blood pressure
    change in cardiovascular risk factors for the child
    non-HDL
    change in cardiovascular risk factors for the child
    LDL
    change in cardiovascular risk factors for the child
    triglyceride
    change in cardiovascular risk factors for the child
    HDL
    change in cardiovascular risk factors for the child
    TC
    change in cardiovascular risk factors for the child
    glucose
    change in cardiovascular risk factors for the child
    hsCRP
    change in cardiovascular risk factors for the child
    HbA1C
    change in cardiovascular risk factors for the child
    Dietary Quality
    total caloric intake captured through the Automated Self-Administered 24-hour Dietary Assessment Tool of the child and mother at 2 years of age

    Full Information

    First Posted
    June 2, 2022
    Last Updated
    July 25, 2022
    Sponsor
    The Hospital for Sick Children
    Collaborators
    Toronto Public Health, University of Toronto, Unity Health Toronto, Applied Health Research Centre, McMaster University, Pediatric Alliance of Ontario, Canadian Paediatric Society, Queen Mary University of London
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05477628
    Brief Title
    Nutrition Recommendation Intervention trialS in Children's Healthcare
    Acronym
    NuRISH
    Official Title
    Nutrition Recommendation Intervention trialS in Children's Healthcare
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 1, 2022 (Anticipated)
    Primary Completion Date
    December 2026 (Anticipated)
    Study Completion Date
    December 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    The Hospital for Sick Children
    Collaborators
    Toronto Public Health, University of Toronto, Unity Health Toronto, Applied Health Research Centre, McMaster University, Pediatric Alliance of Ontario, Canadian Paediatric Society, Queen Mary University of London

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    NuRISH is a suite of clinical trials for children from low-income families which will determine whether primary healthcare prescription for: 1) Optimal breastfeeding with support from a mobile lactation consultant vs. usual care and 2) High-quality childcare starting at 1 year vs. usual care can prevent childhood obesity, and improve cardiovascular, developmental and mental health at 2 years of age.
    Detailed Description
    Canada's children are falling behind. One in 4 are overweight or obese and more than 1 in 3 have factors that put them at risk for cardiovascular disease as adults. Children from low income families are 70% more likely to be overweight or obese. Research across disciplines has shown that early life nutrition has profound effects on childhood obesity, development, mental health, and lifetime success. Optimizing early life nutrition to reduce inequalities in childhood obesity and its consequences is a promising approach. Through this application, we will be using a longitudinal factorial design within an ongoing cohort study(TARGet Kids!). The longitudinal factorial design involves randomizing the same children to multiple interventions, providing the opportunity to evaluate the effect of individual interventions as well as the multiplicative effects of a combination of interventions over time. This design increases the feasibility and lowers the cost relative to conducting 2 separate trials. This will be a pragmatic, randomized, longitudinal factorial Trials within Cohorts (TwiCs) clinical trial. This study will be a direct comparison of two primary healthcare interventions provided randomly at the individual level: 1) Lactation Consultant (LC) support vs. usual care; 2) Childcare Navigator (CN) support vs. usual care.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Obesity, Childhood, Nutrition, Health Risk Behaviors, Breastfeeding, Exclusive Breastfeeding, Diabetes
    Keywords
    Lower adiposity, Higher breastfeeding self-efficacy, Higher centre-based childcare attendance, Improved child development and mental health, Lower cardiovascular risk factors, Better dietary quality, Lower healthcare and overall societal costs

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Factorial Assignment
    Model Description
    This will be a pragmatic, randomized, longitudinal factorial Trials within Cohorts (TwiCs) clinical trial. This study will be a direct comparison of two HCP prescriptions provided randomly at the individual level: 1) Optimal breastfeeding with mobile lactation consultant support vs. usual care and 2) High-quality childcare starting at 1 year of age vs. usual care. We will combine TwiCs methods with a longitudinal factorial design to enhance the integration of cohort study and factorial trial designs.
    Masking
    Outcomes Assessor
    Masking Description
    To reduce the risk of bias, all research assistants who collect baseline and outcome data will be blinded. All other study personnel, including data analysts, will also be blinded to group allocation. Due to the nature of the intervention, children and parents cannot be blinded, but they will be blinded to trial hypotheses. Healthcare providers who provide the interventions also cannot be blinded.
    Allocation
    Randomized
    Enrollment
    620 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Control Group
    Arm Type
    Placebo Comparator
    Arm Description
    Participants who are randomized to the control group will receive usual care from their health care practitioners.
    Arm Title
    Intervention Group
    Arm Type
    Experimental
    Arm Description
    Participants who are randomized to Intervention Group will receive one of three possible "scenarios": 1) Childcare Navigator Support, 2) Breastfeeding support via Lactation Consultant, 3) both Childcare Navigator Support and Breastfeeding support via Lactation.
    Intervention Type
    Other
    Intervention Name(s)
    Childcare Navigator
    Other Intervention Name(s)
    (CN)
    Intervention Description
    Participants will be contacted by the CN to assist with access to centre-based childcare after enrolment. The CN will: a) educate the family on the benefits of centre based childcare; b) facilitate placement of the child on waiting lists for funding and centre based childcare placement in their neighbourhood with the aim of having full-time centre based childcare start at 1 year of age; and c) work with the family to overcome barriers to childcare placement prior to and during childcare. It is expected that the child will be in full-time centre-based childcare for a minimum of 12 months. Control: All children randomized to the control condition will receive age-appropriate nutritional recommendations as part of routine healthcare according to the Rourke Baby Record.
    Intervention Type
    Other
    Intervention Name(s)
    Lactation Consultant
    Other Intervention Name(s)
    (LC)
    Intervention Description
    Participants will be contacted by the LC on the same day as their first primary healthcare visit. They will also receive age-appropriate nutrition recommendations according to the Rourke Baby Record. The LC will be an International Board Certified Lactation Consultant (IBCLC) who will provide scheduled and on-call visits, along with phone calls, video conferencing, and text messaging as needed to support exclusive breastfeeding (using virtual care modalities as appropriate during COVID-19). The LC will contact the family once per week for the first 4 weeks to support breastfeeding technique and help with breastfeeding problems such as latching difficulties, painful nursing, and low milk production, monthly thereafter and provide on-call support as required to support exclusive breastfeeding through 6 months of age. Control: All children randomized to the control condition will receive age-appropriate nutritional recommendations as part of routine healthcare.
    Intervention Type
    Other
    Intervention Name(s)
    Lactation Consultant Support and Childcare Navigator Support
    Other Intervention Name(s)
    LC+CN
    Intervention Description
    This intervention is a combination of the two interventions described above.
    Intervention Type
    Other
    Intervention Name(s)
    Control Group
    Intervention Description
    All children randomized to the control condition will receive age-appropriate nutritional recommendations as part of routine healthcare.
    Primary Outcome Measure Information:
    Title
    zBMI
    Description
    The primary outcome measure will be age and sex standardized BMI z-score (zBMI), which will be measured at the 2-year primary healthcare visit. zBMI is an important outcome that is predictive of adiposity in later childhood, adolescence and adulthood. Data including birthweight and length, and repeated measures of weight and length will be used to calculate zBMI growth trajectories.
    Time Frame
    2-year primary healthcare visit
    Secondary Outcome Measure Information:
    Title
    breastfeeding self-efficacy
    Description
    change in breastfeeding self-efficacy measured by lactation consultant logs
    Time Frame
    6 months
    Title
    exclusive breastfeeding duration
    Description
    change in exclusive breastfeeding duration
    Time Frame
    6 months
    Title
    Childcare attendance
    Description
    change in centre-based childcare attendance measured by attendance logs
    Time Frame
    2 years of age
    Title
    cognitive development
    Description
    To capture child's development, the Ages and Stages Questionnaire will be administered. The Ages and Stages Questionnaire identifies infants, toddlers and preschool aged children at risk of a developmental delay in five developmental domains: Communication, Gross Motor, Fine Motor, Problem Solving and Personal Social Behaviour. Each domain consists of six questions about important age-specific developmental milestones. If a child scores between 1 and 2 below the normative mean on any domain, rescreening is recommended. When a child scores 1 below the normative mean on two or more domains, or 2 below the normative mean on at least one domain, a referral to a health care professional is recommended.
    Time Frame
    2 years of age
    Title
    maternal mental health
    Description
    change in maternal mental health, measured by the Edinburgh Postnatal Depression Scale at 2 years of age. The scale was developed for screening postpartum women in outpatient, home visiting settings, or at the 6 -8 week postpartum examination. Consisting of 10 questions, each response is scored 0, 1, 2, or 3 according to increased severity of the symptom. Items marked with an asterisk (*) are reverse scored (i.e., 3, 2, 1, and 0). The total score is determined by adding together the scores for each of the 10 items. A woman scoring 9 or more points or indicating any suicidal ideation - that is she scores 1 or higher on question #10 - should be referred immediately for follow-up. Even if a woman scores less than 9, if the clinician feels the client is suffering from depression, an appropriate referral should be made.
    Time Frame
    2 years of age
    Title
    mental health
    Description
    Child's mental health captured by the Strengths and Difficulties Questionnaire. The questionnaire consists of 25 items subdivided into four difficulties scales, emotional symptoms, conduct problems, inattention-hyperactivity and peer problems, and a separate fifth strength scale, prosocial behavior. All subscales have five questions. Each item has to be scored on a 3-point scale with 0 = 'not true', 1 = 'somewhat true' and 2 = 'certainly true'. A higher score indicates more emotional and behavioral problems.
    Time Frame
    2 years of age
    Title
    blood pressure
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    non-HDL
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    LDL
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    triglyceride
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    HDL
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    TC
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    glucose
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    hsCRP
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    HbA1C
    Description
    change in cardiovascular risk factors for the child
    Time Frame
    2 years of age
    Title
    Dietary Quality
    Description
    total caloric intake captured through the Automated Self-Administered 24-hour Dietary Assessment Tool of the child and mother at 2 years of age
    Time Frame
    2 years of age

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Day
    Maximum Age & Unit of Time
    1 Week
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Healthy by parental report <32 weeks gestation 0-1 week of age First birth /first time parents Family income <$70,000 Exclusion Criteria: Children with a syndrome associated with obesity or developmental delay
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mateenah M Jaleel, BSc
    Phone
    6476745016
    Email
    mateenah.jaleel@sickkids.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jonathon Maguire, MD,FRCPC,MSc
    Organizational Affiliation
    The Hospital for Sick Children
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Nutrition Recommendation Intervention trialS in Children's Healthcare

    We'll reach out to this number within 24 hrs