UK research priorities for Developmental Coordination Disorder (DCD)

Working with stakeholders we will co-create a top 10 list of research priorities for DCD, ensuring future research is relevant and beneficial.

The importance of research priorities

Establishing research priorities ensures the efficient use of limited resources and directs efforts to the most impactful areas. While research priorities exist for some neurodevelopmental disorders, none have been set for Developmental Coordination Disorder (DCD) in the UK.

DCD

DCD is a lifelong condition affecting approximately 2-6% of children in the UK, with 70% experiencing significant motor difficulties into adulthood. Given its prevalence, there is an urgent need to guide research efforts to address the needs of those affected.

The need for priorities

Without identified research priorities, efforts may fail to meet the needs of individuals with DCD, practitioners, funders and policy makers. Setting these priorities will ensure future funding and research generate meaningful and applicable results.

The James Lind Alliance (JLA) approach

The JLA, a UK-based non-profit initiative, offers a structured process for setting research priorities. This involves bringing together individuals with lived experiences, carers, practitioners and other stakeholders as equal partners to co-create a top 10 list of research priorities.

Our project goals

We aim to utilise the JLA's approach to:

identify the uncertainties and unanswered questions faced by stakeholders
prioritise the top 10 most important research questions for the UK
encourage funders, researchers, and policy makers to align their efforts with these identified priorities

We will engage UK DCD academics, children with DCD and their families/carers, education providers, adults with DCD, third sector organisations and health and social care professionals to ensure a comprehensive and inclusive process.