PreM: School-based Support for Pre-school Aged Children With Developmental Disabilities and Delays

Sponsor
University of Illinois at Chicago (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06145659
Collaborator
National Institutes of Health (NIH) (NIH), National Institute of Nursing Research (NINR) (NIH)
320
2
58

Study Details

Study Description

Brief Summary

This proposal aims to test whether a proposed community-clinical linkage (CCL), an educational-medical linkage model, improves access to school-based services and subsequent child, parent, family and health service outcomes and offers a promising strategy to address longstanding racial, ethnic and income health care disparities among families with preschool children with developmental delays and disabilities. The investigators designed an educational-clinical linkage model, Preschool and Me (PreM) which incorporates key components of a CCL. It also utilizes a personalized medical-education care plan with remote lay navigator support to increase access to school-based services.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Preschool and Me
N/A

Detailed Description

Participants (n=320) will be randomized to either: 1) 6 months of PreM (intervention group) or 2) a waitlist control arm receiving the intervention after a 6-month delay. All participants will be followed for 12 months with data collection occurring at 4 timepoints (baseline, 3-, 6- and 12-months). There will also be a simultaneously conducted mixed-methods implementation evaluation focusing on implementation outcomes to serve as indicators for implementation success; measures of implementation quality; and intermediate outcomes to understand and address successes and failures in relation to clinical outcomes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
320 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Educational-Clinical Linkage to Improve Health Equity for Children With Developmental Delays and Disabilities From Marginalized Communities
Anticipated Study Start Date :
Feb 1, 2024
Anticipated Primary Completion Date :
Aug 1, 2028
Anticipated Study Completion Date :
Dec 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: Linkage Model

Preschool and Me intervention

Behavioral: Preschool and Me
Utilizes patient navigation services and a medical-educational care plan to support linkages between medical and educational systems

No Intervention: Treatment as Usual

Preschool and Me intervention is not used

Outcome Measures

Primary Outcome Measures

  1. Percent of children who enroll in a designated early childhood special education (ECSE) program [Up to 12 months]

    Increased access to early childhood special education (ECSE) as measured by enrollment in early childhood education program

  2. Percent of children who receive ECSE-based therapies [Up to 12 months]

    Increased access to early childhood special education (ECSE) services as measured by receipt of ECSE-based services

  3. Timeliness of ECSE services [Up to 12 months]

    Calculate the time (number of days) from a child's 3rd birthday to 1) date of ECSE request; 2) date of IEP eligibility meeting; 3) attendance at preschool (first day); and 4) start date of first ECSE-based therapy for those found eligible.

  4. Percent of children who complete each step of ECSE process [up to 12 months]

    Percent of children who complete each step of ECSE process

Secondary Outcome Measures

  1. Child quality of life [Baseline, 12 month follow up]

    Vineland Adaptive Behavior Scales, Third Edition (Vineland-3) is a measure of communication, daily living skills, and socialization skils which is administered in a semi-structured parent interview format. Items assess the individual's behavior in these domains and are rated according to the frequency with which behaviors are performed without help or prompting (i.e., "Never," "Sometimes" or "Usually"). The raw scores are converted to standard scores (mean = 100, SD = 15; range 40 to 160), and higher scores indicate better adaptive functioning.

  2. Child sleep habits [Baseline, 12 month follow up]

    Exploratory outcome assessing regulation of sleep using Family Inventory of Sleep Habit (FISH). The FISH is a 12-item survey of sleep habits which is scored on a 5-point scale. A higher score indicates better sleep hygiene.

  3. Parenting stress [Baseline, 12 month follow up]

    Caregiver Strain Short Form consists of 11 items assessing the level of strain caregivers experience in caring for their child consisting of the following factors: objective strain, subjective internalized strain, and subjective externalized strain. Items are rated on a 5-point Likert-type scale that ranges from 1 (not at all) to 5 (very much). Higher scores represent greater strain.

  4. Family Functioning [Baseline, 12 month follow up]

    General Functioning 12-item subscale (GF12) of The McMaster Family Assessment Device (FAD); The FAD consists of 7 scales: affective involvement, affective responsiveness, behavioral control, communication, problem solving, roles and general family functioning. Participants are asked to rate how well each statement describes their family on a 4 point scale. Higher scores indicate worse levels of family functioning.

  5. Family-centered care self-assessment tool [Baseline, 12 month follow up]

    Family Centered Care Assessment Tool Community Systems of Services and Supports and Community Systems Integration and Care Coordination examines a participants perception of family-centered care received at their healthcare facility; Each item is rated on a 4-point Likert scale (1= never; 4= always) with higher scores indicating a greater perception of family-centered care.

  6. Satisfaction with the Interpersonal Relationship with the Navigator (PSN-I) [Up to 6 months]

    Satisfaction with the Interpersonal Relationship with the Navigator (PSN-I) is a 9 item questionnaire that examines participants perception of their PreM navigator; Each item is rated on a 5-point Likert scale with a higher score indicating a higher satisfaction with their interpersonal relationship with the patient navigator.

  7. Acceptability of Intervention Measure [Up to 6 months]

    Acceptability of Intervention Measure examines participants acceptability of PreM; Each item is rated on a 5-point Likert scale with a higher score indicating a greater acceptability

  8. Adoption [up to 6 months]

    Ratio of number of Primary Care Providers (PCPs) who referred to Preschool and Me (PreM) to total number of PCPs

  9. Intervention Appropriateness Measure (IAM) [up to 6 months]

    Intervention Appropriate Measure examines perception of the appropriateness of PreM; Each item is rated on a 5-point Likert scale with a higher score indicating a greater perception of appropriateness

  10. Penetration [up to 6 months]

    Ratio of number of caregivers contacted by Patient Navigator (PN) to number of caregivers referred

  11. Feasibility of Intervention Measure [up to 6 months]

    Feasibility of Intervention Measure examines perception of the feasibility of PreM; Each item is rated on a 5-point Likert scale with a higher score indicating a greater perception of feasibility

  12. Fidelity [up to 6 months]

    Per family ratio of number of PN activities conducted to number of activities that should be conducted according to protocol/job aid

  13. Cost [up to 6 months]

    Time estimates of training and supervision; Per family time estimates associated with PN activities

Other Outcome Measures

  1. Positive Protective Factors (Resilience, Social Connections, Concrete Support in Time of Need) [6, 12 months]

    Parent Assessment of Protective Factors is a measure to assess participants' self-reported beliefs, feelings, and behaviors in the areas of Resilience, Social Connections, Concrete Support in Time of Need. Items are scored on a 5 point Likert scales with higher scores indicating a higher perceived strength level.

  2. Parent Patient Activation Measure Parent Patient Activation Measure Parent Patient Activation Measure [6, 12 months]

    Parent Patient Activation Measure assesses perceived knowledge, skills, and confidence in managing child's care. Items are scored using a 4-point Likert scale (1 = disagree strongly; 4 = agree strongly). Higher scores correspond to higher activation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
36 Months and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Parent-child dyads who meet inclusion criteria will be enrolled.

Child inclusion criteria are:
  1. Meets age requirements for early childhood special education (ECSE) services for Illinois (i.e., 36-59 months of age by September 1 of current school year);

  2. diagnosed with a developmental delay or disability (DD) or determined to be at risk for DD (clinical concerns raised by primary care provider/healthcare provider or by parents at the time of enrollment);

  3. screens positive on the Survey of Wellbeing of Young Children, a validated screening instrument for DD available in English and Spanish;

  4. is not receiving any ECSE services.

Exclusion Criteria:

if inclusion criteria is met, no other exclusion criteria will be applied.

Parent inclusion criteria are:
  1. aged18 years or older;

  2. lives in Chicago;

  3. speaks English or Spanish;

  4. a legal guardian of a child who meets inclusion criteria.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Illinois at Chicago
  • National Institutes of Health (NIH)
  • National Institute of Nursing Research (NINR)

Investigators

  • Principal Investigator: Reshma Shah, MD, MPH, University of Illinois at Chicago

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Illinois at Chicago
ClinicalTrials.gov Identifier:
NCT06145659
Other Study ID Numbers:
  • 2023-1361
  • R01NR021155
First Posted:
Nov 24, 2023
Last Update Posted:
Nov 24, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Illinois at Chicago

Study Results

No Results Posted as of Nov 24, 2023