N/A
N=64,382
Care Coordination for Children With Disabilities
Experiences With Health Care Coordination
Bottom Line
View on ClinicalTrials.gov: NCT02304380 ↗Enrolled (actual)
64,382
Serious AEs
0.0%
Results posted
Jun 2020
Primary outcome: Primary: Percent of Caregivers Who Reported That Their Child Has a Designated Care Coordinator — 864 Participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Pediatric, Adult, Older Adult · 3+ yrs
- Sex
- All
- Sponsor
- University of North Carolina, Chapel Hill
- Primary completion
- Nov 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percent of Caregivers Who Reported That Their Child Has a Designated Care Coordinator |
864 | — |
| SECONDARY Percent of Caregivers Who Reported That Their Care Coordinator Asked About Caregiver Concerns and Changes in the Child's Health |
261 | — |
| SECONDARY Percent of Caregivers Who Reported Receiving a Comprehensive Written After-visit Summary in the Past 12 Months |
523 | — |
| SECONDARY Percent of Caregivers Who Reported That Their Child's Primary Care Provider Created a Shared Care Plan for Their Child |
985 | — |
| SECONDARY Use of One or More Well-child Visits <=6 Years Old |
9,235; 25,106 | — |
| SECONDARY Use of One or More Well-child Visits >=12 Years Old |
24,342; 72,803 | — |
| SECONDARY Indicator of Use of Primary Care |
49,358; 142,579 | — |
| SECONDARY Use of Outpatient Medicaid Visits to Other Behavioral Health Providers |
49,358; 142,579 | — |
| SECONDARY Emergency Department Use |
49,358; 142,579 | — |
| SECONDARY Use of Hospitalizations |
49,358; 142,579 | — |
| SECONDARY Follow-up Within 7 Days After Hospitalization |
10,602; 31,968 | — |
| SECONDARY Follow-up Within 30 Days After Hospitalization |
10,602; 31,968 | — |
| SECONDARY Hospital Readmissions Within 30 Days After Discharge |
10,602; 31,968 | — |
| SECONDARY Hospitalization for Mental Illness |
49,358; 142,579 | — |
| SECONDARY Follow-up Within 7 Days After Hospitalization for Mental Illness |
1,484; 7,409 | — |
| SECONDARY Follow-up Within 30 Days After Hospitalization for Mental Illness |
1,484; 7,409 | — |
| SECONDARY Medication Use - Antidepressants |
49,358; 142,579 | — |
| SECONDARY Medication Use - Anticonvulsants |
49,358; 142,579 | — |
| SECONDARY Medication Use - Anti-anxiety Medications |
49,358; 142,579 | — |
| SECONDARY Medication Use - Anti-psychotic Medications |
49,358; 142,579 | — |
| SECONDARY Medication Use - ADHD Medications |
49,358; 142,579 | — |
| SECONDARY Medication Use - Asthma Medications |
49,358; 142,579 | — |
| SECONDARY Follow-up Within 30 Days After ADHD Prescription |
75,757; 214,253 | — |
Summary
The proposed study uses a recent policy change in Ohio as a natural experiment to assess outcomes and experiences of children who qualify for Medicaid under the Aged, Blind, Disabled category and their caregivers in an ACO model of care compared to their previous outcomes and experiences in a traditional fee-for-service model.
Eligibility Criteria
Inclusion Criteria
Stakeholder Interviews
- Be associated with the ACO as ACO leadership, a care coordinator, a payor or policy-maker.
Caregiver Interviews
- Currently live in south-central Ohio
- Have lived in south-central Ohio since July 2012
- Be a caregiver of a child ages 3-18 who qualifies for Medicaid under the Aged, Blind, and Disabled category
Focus Groups, Caregivers and Youth
- Currently live in south-central Ohio
- Have lived in south-central Ohio since July 2012
- Be a caregiver of a child ages 3-18 who qualifies for Medicaid under the Aged, Blind, and Disabled (ABD) category, who receives care at Nationwide Children's Hospital, Partners for Kids
- For youth focus groups, be a child ages 14-18 who qualifies for Medicaid under the Aged, Blind, and Disabled category, who is intellectually capable of participating in focus groups, and who receives care at Nationwide Children's Hospital, Partners for Kids
Exclusion Criteria
- Non-English-speaking
- For youth focus groups, intellectual disabilities that preclude being able to participate in a focus group
Data sourced from ClinicalTrials.gov (NCT02304380). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.