Social Navigator to Address Social Determinants of Health in Pediatrics

Sponsor
Children's Hospital of Eastern Ontario (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05900505
Collaborator
(none)
104
1
2
18
5.8

Study Details

Study Description

Brief Summary

It is crucial to understand the social and economic context in which children and youth live; their social determinants of health (SDH). Although this is well recognized, many health care providers do not address SDH because of the lack of easily accessible resources once social needs are identified.

Social workers (SW) have the ability to support families once a social need has been identified. However, not every clinic has a SW, and even those that do often struggle to meet the needs of all the families requiring support.

The use of social navigators (SN) is an innovative solution for an unmet need. SN models have been successful in primary care settings, but, to date, have not been adapted to address the SDH needs of children and their families receiving care in pediatric specialty care settings. We will implement the first of its kind pediatric SN clinic at the Children's Hospital of Eastern Ontario (CHEO): "Navigating Social Resources for Children's Health" (NSRCH). Our study will evaluate NSRCH - an innovative, transferable, and low-cost pediatric-specific SN model. Our goal is to support families with SDH needs to access timely, appropriate supports and resources via NSRCH.

Condition or Disease Intervention/Treatment Phase
  • Other: Social Navigator
N/A

Detailed Description

In Phase 1 of our study, potential patient-participants will be identified from the type 1 diabetes and type 2 diabetes clinics at CHEO in the following way: the study coordinator will manually screen upcoming patients in the diabetes clinic schedules in Epic. Then, a cover letter and study information sheet will be sent to potential patient-participants (or they would be approached by a study coordinator in-person during the clinic visit). They will follow up with the family to explain the study, answer any questions, confirm interest. Interested families will be asked to complete the Phase 1 Screening Tool.

The study coordinator will be automatically notified of all positive screens (at least 1 identified social need), and then contact the respective families to invite them to participate in Phase 2 of the study and obtain informed consent.

At baseline, the coordinator will collect baseline data and have the families complete the Quality of Life - Brief Version (WHOQOL-BREF) and Baseline Questionnaire. After the visit, participants will be randomized to the intervention or control groups using the randomization module in REDCap. A referral will then be forwarded to either the SN or SW. All clinic visits between baseline and follow up will be scheduled directly by the SN or SW. The SN and the SW will be asked to complete a checklist for each participant consultation, and the results will be summarized by the coordinator.

Participants will be contacted by a coordinator for a follow up visit at 6 months. At which time, they will collect follow-up data and have the families complete the Phase 1 Screening Tool, WHOQOL-BREF, and CSQ.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
104 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Addressing Child and Family Social Determinants of Health Needs With Social Navigation: Navigating Social Resources for Children's Health "NSRCH" Clinic
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Participants in the intervention group will be referred to a social navigator to address their identified social needs.

Other: Social Navigator
The social navigator will assess patient/family needs and help them to access community resources (specific to their community) to address these, while promoting their engagement and self-efficacy.

No Intervention: Control Group

Participants in the control group will be referred to a social worker, as per standard care.

Outcome Measures

Primary Outcome Measures

  1. To compare participant satisfaction with NSRCH (social navigator) vs. standard care (social worker), as measured by the Client Satisfaction Questionnaire (CSQ). [6 months]

    Client Satisfaction Questionnaire: Participant satisfaction will be determined using a validated Client Satisfaction Questionnaire (CSQ). The CSQ is scored on a scale of 8 to 32, with higher scores indicating higher satisfaction.

Secondary Outcome Measures

  1. To compare the time to access NSRCH (social navigator) vs. standard care (social worker). [6 months]

  2. To compare the rate of attendance to NSRCH (social navigator) vs. standard care (social worker) visits. [6 months]

  3. To compare the number of community resources accessed by participants relative to the number of community resources to which they were referred by NSRCH (social navigator) vs. standard care (social worker). [6 months]

  4. To compare whether resources provided to the participants corresponded to their identified social needs at NSRCH (social navigator) vs. standard care (social worker). [6 months]

    The social workers and social navigator will be required to indicate which resources were referred to each participant. They will also be required to indicate if the resource corresponds to one or more of the participant's identified social need(s). The mean percentage of resources that correspond to identified social needs will be compared between NSRCH (social navigator) and standard care (social workers).

  5. To compare change in Quality of Life (QOL) of participants (pre/post intervention) referred to NSRCH (social navigator) vs standard care (social worker), as measured by the WHOQOL-BREF. [6 months]

    Quality of Life: change in quality of life from baseline to end of study (pre/post intervention) will be compared between the NSRCH and standard care groups. Quality of life will be assessed using the World Health Organization Quality of Life - Brief Version (WHOQOL-BREF). The WHOQOL-BREF is a quality of life assessment developed by the WHOQOL Group with fifteen international field centres, simultaneously, in an attempt to develop a quality of life assessment that would be applicable cross-culturally. Higher scores denote a higher quality of life. This measure provides 4 domain scores, one for each domain in which quality of life is assessed: physical (raw score 7-35), psychological (raw score 6-30), social relationships (raw score 3-15), and environment (raw score 8-40). Raw scores can also be transformed to reflect scores of 4-20 or 0-100.

Other Outcome Measures

  1. To compare NSRCH (social navigator) vs. standard care (social worker) with respect to changes in glycemic control. [6 months]

    To compare NSRCH (social navigator) vs. standard care (social worker) with respect to changes in glycemic control: Glycated hemoglobin (HbA1c, (%)), percent time in range (TIR - percentage of time in previous 14 days spent within target glucose range of 70-180 mg/dL or 3.9-10 mmol/L), and glucose management indicator (GMI, %). Taken together, these indicators reflect overall glycemic control.

  2. Change in Social Determinants of Health (SDH) Screening Status [6 months]

    To compare the change in positive screen status on the SDH screening tool from baseline to 6 months, in NSRCH (social navigator) vs. standard care (social worker).

  3. To compare the resource cost of the social navigator compared to the social worker. [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Phase 1

  • Age between 0-17 years

  • Patient in the Type 1 diabetes (T1D) or Type 2 diabetes (T2D) clinics at CHEO

  • Dyad participation (parent/caregiver-child)

Phase 2

  • Meet the Phase 1 eligibility criteria

  • At least 1 positive response on the SDH screening tool

Exclusion Criteria:
  • Active social work client at the time of the screening, defined as individuals who self- identify as having active follow up with a diabetes SW to address social need(s)

  • Unable or unwilling to provide i) implied consent for the completion of the SDH screening tool and/or ii) written informed consent for participation in the randomized trial

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital of Eastern Ontario - Research Institute Ottawa Ontario Canada K1H 8L1

Sponsors and Collaborators

  • Children's Hospital of Eastern Ontario

Investigators

  • Principal Investigator: Caroline Zuijdwijk, MD, Children's Hospital of Eastern Ontario

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Caroline Zuijdwijk, Pediatric Endocrinologist, Children's Hospital of Eastern Ontario
ClinicalTrials.gov Identifier:
NCT05900505
Other Study ID Numbers:
  • 22/65X
First Posted:
Jun 12, 2023
Last Update Posted:
Jun 15, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 15, 2023