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

Educational-Clinical Linkage to Improve Health Equity for Children With Developmental Delays and Disabilities From Marginalized Communities

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06145659
Acronym
PreM
Enrollment
320
Registered
2023-11-24
Start date
2024-03-25
Completion date
2029-01-01
Last updated
2026-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Developmental Delay

Keywords

primary care, implementation, linkage

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.

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.

Interventions

BEHAVIORALPreschool and Me

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

Sponsors

University of Illinois at Chicago
Lead SponsorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
National Institute of Nursing Research (NINR)
CollaboratorNIH

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
36 Months to No maximum
Healthy volunteers
Yes

Inclusion criteria

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., 3-5 years old); 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. is not receiving any ECSE services.

Exclusion criteria

if inclusion criteria is met, no other

Design outcomes

Primary

MeasureTime frameDescription
Timeliness of ECSE servicesUp to 12 monthsCalculate the time (number of days) from a child's 3rd birthday to 1) date of Individualized Education Plan (IEP) request; 2) date of IEP eligibility meeting; 3) attendance at preschool (first day); and 4) start date of first school-based therapy for those found eligible.
Percent of children who complete each step of IEP processup to 12 monthsPercent of children who complete each step of IEP process
Percent of children who receive school-based therapiesUp to 12 monthsIncreased access to early childhood special education (ECSE) services as measured by receipt of school-based services
Percent of children who enroll in a designated early childhood special education (ECSE) program or Chicago Public SchoolUp to 12 monthsIncreased access to early childhood special education (ECSE) as measured by enrollment in designated Chicago Early Learning Education Program or Chicago Public School

Secondary

MeasureTime frameDescription
Satisfaction with the Interpersonal Relationship with the Navigator (PSN-I)Up to 6 monthsSatisfaction 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.
Acceptability of Intervention MeasureUp to 6 monthsAcceptability 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
Adoptionup to 6 monthsRatio of number of Primary Care Providers (PCPs) who referred to Preschool and Me (PreM) to total number of PCPs
Intervention Appropriateness Measure (IAM)up to 6 monthsIntervention 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
Penetrationup to 6 monthsRatio of number of caregivers contacted by Patient Navigator (PN) to number of caregivers referred
Child sleep habitsBaseline, 12 month follow upExploratory outcome assessing sleep disturbance using the PROMIS Parent Proxy Sleep Disturbance questionnaire. This 8 question survey of sleep disturbances is scored on a 5-point scale. A higher score indicates poorer sleep hygiene.
Fidelityup to 6 monthsPer family ratio of number of PN activities conducted to number of activities that should be conducted according to protocol/job aid
Costup to 6 monthsTime estimates of training and supervision; Per family time estimates associated with PN activities
Parental Quality of LifeBaseline and 12 monthsParent Quality of Life will be assessed using PROMIS Item Bank v2.0 - Ability to Participate in Social Roles and Activities - Short Form 6a which examines satisfaction with performing one's social roles and activities. Higher scores reflect more of the measured construct (i.e., ability to participate in social roles and activities).
Child quality of lifeBaseline, 12 month follow upChild quality of life will be assessed using questionnaires from the Patient Reported Outcomes Measurement Information System (PROMIS). The questionnaires will examine quality of life under the follow domains: well being, relationships, emotional distress, and health. The questionnaires utilize a 5-point likert scale with higher scores reflecting more of the measured construct within the domain.
Feasibility of Intervention Measureup to 6 monthsFeasibility 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
Parenting stressBaseline, 12 month follow upCaregiver 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.
Family FunctioningBaseline, 12 month follow upGeneral 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.
Family-centered care self-assessment toolBaseline, 12 month follow upFamily 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.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORReshma Shah, MD, MPH

University of Illinois at Chicago

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026