- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05091957
Connecting Families
CONNECTING FAMILIES: A Randomized Controlled Trial of Primary Care Poverty Screening and Financial Support Navigation for Families of Young Children
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
INTRODUCTION AND IMPORTANCE: Poverty and financial strain have profound and long-lasting negative impacts on both parent and child health, contributing to substantial health disparities. As the first contact with the health system for most families, primary care providers are uniquely positioned to address child poverty in clinical settings.
Many professional health organizations recommend that healthcare providers identify and address social determinants of health, but there is little evidence regarding the impact of effective interventions. Social systems are frequently complex and difficult to navigate; for example, low income Canadians are known to have lower tax filing rates than the general population. Therefore, many families may not be accessing all social benefits to which they are entitled. The investigators propose to rigorously test a poverty reduction intervention (navigation of financial supports) embedded in primary care using a randomized controlled trial to evaluate the impact on parent and child health outcomes. Results of our pilot study demonstrated feasibility and will inform our proposed full trial.
METHODS: Study Design: A multi-site, pragmatic, blinded, superiority, parallel-group randomized controlled trial will be conducted.
Participants: Families of children ages (from birth to 2 years), screening positive for the question "Do you ever have difficulty making ends meet at the end of the month?", identified as a good predictor of poverty.
Intervention and Active Comparator: Families will be randomly allocated to the intervention or active comparator group. Parents in the intervention group will have a review of their social needs and resources with a trained Community Service Worker (CSW) with a thorough understanding of potential income supports and community agencies and will assist the parent to access financially related social benefits for which they are eligible. All participants will receive a written summary of available resources.
Outcomes: The primary outcome, measured 6 months after enrollment, is parenting stress, as measured by the Parenting Stress Index-Short Form. Secondary outcomes are change in: a) self-reported after-tax household income; b) household food security; c) parent depression; d) child development; e) child social, emotional and behavioural health; f) Community Service Worker workload; g) health care utilization.
TEAM EXPERTISE: The study is a collaboration between TARGet Kids!, (a well-established child-focused primary care practice-based research network) and integrated Knowledge Users (parents, administrators and policy makers). The research team has expertise in child health, pragmatic trials and social determinants of health.
EXPECTED OUTCOME: Results from this research will address a critical evidence gap regarding a feasible and scalable intervention to address child poverty in the primary care practice setting. Leveraging primary preventive care in early childhood, which is accessed by almost all families, will provide powerful opportunities for implementation. Effective interventions to address child poverty and financial strain in clinical practice have the potential to influence child health trajectories over their life course.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imaan Bayoumi
- Phone Number: 613-331-2371
- Email: bayoumi@queensu.ca
Study Contact Backup
- Name: Cornelia Borkhoff
- Phone Number: 647-883-9270
- Email: cory.borkhoff@sickkids.ca
Study Locations
-
-
Ontario
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Kingston, Ontario, Canada, K7L 5E9
- Recruiting
- Queen's Family Health Team
-
Contact:
- Dane Mauer-Vakil
- Phone Number: 613-533-9303
- Email: vdm@queensu.ca
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Parents of children (younger than 3 years) attending a regularly scheduled primary care visit.
- Parents respond affirmatively to the question "Do you ever have difficulty making ends meet at the end of the month?"
- Informed parental consent. Only one child will be enrolled per family. For families with more than one child, we will enroll the youngest eligible child, since literature suggests that impact of reducing family stress may be greater at younger ages; for multiple births, one child will be randomly selected for inclusion.
Exclusion Criteria:
- Parents without legal status in Canada, as they are not eligible for many Canadian social programs.
- Families who are receiving system navigation support, such as from a social worker or public health nurse, or who have received system navigation support within one year prior to enrolment.
- Child with a previously diagnosed developmental disorder, genetic, chromosomal or syndromic condition.
- Child born prematurely (gestational age less than 32 weeks).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Community Support Worker
structured review of participant income supports with a trained CSW, to identify financial needs and benefits for which the family is eligible, including assessment of income and food security, affordability of medications, housing and energy insecurity, and dental care.
The visits will be conducted in person, by telephone or by videoconferencing, according to participant preference and to ensure adherence to COVID-19 pandemic-related criteria.
|
structured review of participant income supports with a trained CSW, to identify financial needs and benefits for which the family is eligible, including assessment of income and food security, affordability of medications, housing and energy insecurity, and dental care.
The visits will be conducted in person, by telephone or by videoconferencing, according to participant preference and to ensure adherence to COVID-19 pandemic-related criteria.
|
|
Active Comparator: Usual Care
There is no clear standard of care and potential for practice variation in clinician responses to identified social need.
Based on the ethical imperative to provide some support to families who identify unmet social needs, the comparator group will receive Usual Care, defined as: Participants in both groups will receive a written summary of available resources.
|
Participants in both groups will receive a written summary of available resources
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parenting Stress Index- Short Form 4
Time Frame: 6 months
|
A 36-item parent-completed questionnaire assessing overall level of stress a person is feeling in their role as a parent.
Scoring yields an overall stress score (range 36-180, with higher scores indicating greater stress) and sub-scores for Parental Distress, Parent-Child Dysfunctional Interaction and Difficult Child (each with range of 5-60) which are summed to generate the total score. .
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self Reported Household Income
Time Frame: 6 months, 12 months
|
Self Reported Household Income from all sources
|
6 months, 12 months
|
|
Participant use of community resources
Time Frame: 6 months, 12 months
|
This is a study specific instrument which assesses participants' receipt of a comprehensive suite of financial benefits (including specific income tax benefits, benefits through social assistance programs) and receipt of emergency food services, childcare subsidy, energy assistance, support for medication and dental costs and housing needs.
|
6 months, 12 months
|
|
Household food security
Time Frame: 6 months, 12 months
|
18-item Household Food Security Survey Module, asks about the household's experiences of food insecurity during the previous year.
Higher scores indicate increased food insecurity and households are classified as food secure, marginally food insecure, moderately food insecure or severely food insecure.
|
6 months, 12 months
|
|
Social Needs
Time Frame: 6 months, 12 months
|
WE Care Survey, s a 10-item questionnaire assessing needs in 4 domains (economic stability, education, neighborhood & physical environment, and food) and whether participants want help with identified needs..
|
6 months, 12 months
|
|
Parent Depression
Time Frame: 6 months, 12 months
|
Patient Health Questionnaire - 9, a 9 item self completed instrument measuring symptoms of depression (range 0-27 with higher scores indicating worse outcome).
|
6 months, 12 months
|
|
Parent anxiety
Time Frame: 6 months, 12 months
|
Generalized Anxiety Disorders-7, a 7 item self completed instrument measuring symptoms of anxiety (range 0-21, with higher scores indicating worse outcome).
|
6 months, 12 months
|
|
Child Social- Emotional Development
Time Frame: 6 months,12 months
|
Ages and Stages: Social Emotional, age specific parent completed questionnaires assessing the child's social and emotional development, in which higher scores indicate better outcomes.
|
6 months,12 months
|
|
Child general development
Time Frame: 6 months, 12 months
|
Ages and Stages-3: age specific parent completed questionnaires assessing the child's s development in 5 developmental areas (Communication, Gross Motor, Fine Motor, Problem Solving, Personal Social), in which higher scores indicate better outcomes.
|
6 months, 12 months
|
|
Pediatric health system utilization
Time Frame: 6 months, 12 months
|
Through linkage with health administrative databases, the investigators will assess differences in health services utilization.
The following administrative databases will be used: Ontario Health Insurance Plan (OHIP) which includes physician billings (fee for service and shadow billing) for physician visits, the National Ambulatory Care Reporting System (NACRS) which includes data on emergency department visits, and the Discharge Abstracts Database (DAD) which includes data on inpatient hospitalizations.
We will assess between-group differences in primary care visits, low acuity emergency department visits (CTAS 3-5), number of hospitalizations and length of stay.For children, primary care visits will be categorized as well-child visits (which may appropriately increase) and other visits (which may be reduced).
|
6 months, 12 months
|
|
Parent health system utilization
Time Frame: 6 months, 12 months
|
Through linkage with health administrative databases, the investigators will assess differences in health services utilization.
The following administrative databases will be used: Ontario Health Insurance Plan (OHIP) which includes physician billings (fee for service and shadow billing) for physician visits, the National Ambulatory Care Reporting System (NACRS) which includes data on emergency department visits, and the Discharge Abstracts Database (DAD) which includes data on inpatient hospitalizations.We will assess between-group differences in primary care visits, low acuity emergency department visits (CTAS 3-5), number of hospitalizations and length of stay.
|
6 months, 12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- FMED-6797-21
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
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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