Service Delivery

Recommendations for post-implementation adaptations to optimize family navigation in pediatric primary care: a qualitative study with parents and navigators.

J et al. (2023) · 2023
★ The Verdict

Parents and navigators created a 38-item wish list that can make Family Navigation faster, friendlier, and fairer.

✓ Read this if BCBAs who help families navigate autism diagnosis in pediatric or community clinics.
✗ Skip if Clinicians only doing direct 1:1 therapy with no navigation role.

01Research in Context

01

What this study did

The team asked parents and navigators what tweaks would make Family Navigation better.

They ran focus groups and interviews in pediatric clinics.

Using the FRAME model, they turned talk into 38 concrete fixes.

02

What they found

People want longer navigation, plain-language autism lessons, and faster ways to reach their navigator.

The 38 ideas range from adding evening hours to sending text reminders before visits.

03

How this fits with other research

Pickard et al. (2019) already showed that co-designing parent programs lowers barriers. This study extends that work by mapping the exact changes families want in primary-care navigation.

Zhu et al. (2026) used CFIR to find that caregiver empowerment speeds autism service uptake. The new list echoes their call for parent education and easy contact.

Vivanti et al. (2018) called for stakeholder-driven tweaks; Wilson et al. (2023) deliver a ready-to-test menu of those tweaks.

04

Why it matters

You can lift items straight from the 38-item list and pilot them next quarter. Start with longer service windows and a group text line. Small, cheap changes may cut the wait for diagnosis and boost family trust.

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Add one extra contact method families asked for—like a dedicated text number—and track how many families use it this week.

02At a glance

Intervention
not applicable
Design
qualitative
Sample size
28
Population
autism spectrum disorder
Finding
not reported

03Original abstract

<h4>Background</h4>Family Navigation (FN) is an evidence-based care management intervention designed to reduce disparities in access to care by providing families with individually tailored support and care coordination. Early data suggest FN is effective, but effectiveness is significantly influenced by both contextual (e.g. setting) and individual (e.g., ethnicity) variables. To better understand how FN could be tailored to address this variability in effectiveness, we set forth to explore proposed adaptations to FN by both navigators and families who received FN.<h4>Methods</h4>This study was a nested qualitative study set within a larger randomized clinical trial of FN to improve access to autism diagnostic services in urban pediatric primary care practices in Massachusetts, Pennsylvania, and Connecticut serving low-income, racial and ethnic minority families. Following FN implementation, key informant interviews were conducted based on the Framework for Reporting Adaptations and Modifications-Expanded (FRAME) with a purposeful sample of parents of children who received FN (n = 21) and navigators (n = 7). Interviews were transcribed verbatim and were coded using framework-guided rapid analysis to categorize proposed adaptations to FN.<h4>Results</h4>Parents and navigators proposed 38 adaptations in four domains: 1) content of the intervention (n = 18), 2) context of the intervention (n = 10), 3) training and evaluation (n = 6), and 4) implementation and scale-up (n = 4). The most frequently endorsed adaptation recommendations focused on content (e.g., lengthening FN, providing parents with additional education on autism and parenting children with autism) and implementation (e.g., increasing access to navigation). Although probes targeted critical feedback, parents and navigators were overwhelmingly positive about FN.<h4>Conclusions</h4>This study builds upon prior FN effectiveness and implementation research by providing concrete areas for adaptation and refinement of the intervention. Recommendations by parents and navigators have the potential to inform improvement of existing navigation programs and development of new programs in similarly underserved populations. These findings are critical as adaptation (cultural and otherwise) is an important principle in the field of health equity. Ultimately, adaptations will need to be tested to determine clinical and implementation effectiveness.<h4>Trial registration</h4>ClinicalTrials.gov, registration number NCT02359084, February 9, 2015.

, 2023 · doi:10.1186/s12875-023-02072-y