A new model for the diagnostic assessment services trajectory for neurodevelopmental conditions

Front Rehabil Sci. 2024 Nov 25:5:1426966. doi: 10.3389/fresc.2024.1426966. eCollection 2024.

Abstract

Purpose: The Canadian province of Québec faces several issues regarding the accessibility and quality of diagnostic assessment and the efficiency and continuity of evaluation, support, and intervention services for children with neurodevelopmental conditions (NDCs). To address these issues, the Ministry of Health and Social Services mandated a research team to initiate the development of a reference trajectory, i.e., a proposed model pathway based on national and international best practices and research, for the diagnostic assessment of NDCs in children aged 0-7 years.

Methods: The present study focused on the development of a logic model to operationalize the diagnostic services trajectory using a community-based participatory research approach and informed by implementation science. This involved representatives from multiple stakeholder groups (e.g., parents, professionals, physicians, administrators, researchers). Project steps included an analysis of best practices from a literature review on diagnostic trajectories, focus groups and interviews with stakeholders, and a validation process to ensure the appropriateness of the final model.

Results: The integration of existing research and stakeholder input resulted in a logic model for a new diagnostic services trajectory for children aged 0-7 years suspected of NDCs and identified key ingredients that should be present in its future implementation.

Conclusion: The proposed model for a diagnostic services trajectory is expected to address several systemic issues identified previously. Its implementation will need to be evaluated to ensure its sustained focus on the needs of families and its ability to promote their quality of life, well-being, and involvement.

Keywords: children aged 0–7; community-based participatory research; diagnostic services; implementation science; neurodevelopmental conditions; services trajectory.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and publication of this article. The research was funded by a Chercheur-boursier Junior 2 grant from the Fonds de recherche du Québec - Santé (FRQS), awarded to Mélina Rivard. Support for translating this work was provided by the Institut universitaire en déficience intellectuelle et en trouble du spectre de l'autisme. Funding for the article processing fee was received from the Décanat de la recherche et de la création at the Université du Québec en Outaouais.