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Best practice principles for management of children with developmental coordination disorder (DCD): results of a
1CanChild Centre for Childhood Disability Research, McMaster University, Hamilton, ON, Canada.
Insights
Developmental Coordination Disorder (DCD) affects children
Area of Science:
- Pediatric Health
- Developmental Psychology
- Rehabilitation Sciences
Background:
- Developmental Coordination Disorder (DCD) is a common condition impacting children's health and education.
- Current research often overlooks population-level best practices for DCD service delivery.
- Identifying guiding principles for DCD management is crucial.
Purpose of the Study:
- To identify principles for best practice and service delivery for children with DCD as a population.
- To map available information on intervention and service delivery for DCD.
Main Methods:
- A scoping review of scholarly and grey literature was conducted.
- Keywords and snowballing techniques identified over 500 documents; 31 met inclusion criteria.
- Data on best practices were extracted and compared by two independent reviewers.
Main Results:
- Two overarching themes and five key principles for DCD service delivery emerged.
- Theme 1: Organizing services for comprehensive child needs (awareness, pathways, staged approach).
- Theme 2: Collaborative, evidence-based service provision (integrating family views, function-focused interventions).
Conclusions:
- Principles for DCD service organization are supported by numerous documents.
- These principles are essential for DCD and may benefit other pediatric disability populations.
- Collaboration among researchers, clinicians, and families is encouraged for intervention design and evaluation.
Background:
Developmental coordination disorder (DCD) is a prevalent health condition that is frequently unrecognized despite the substantial evidence that has accumulated regarding how it affects children's health, education and skills. Most literature focuses on measurement of impairment and description of intervention approaches for individual children; little is known about the principles that should guide best practice and service delivery for children with DCD as a population. The purpose of this study was to identify these principles.
Methods:
A scoping review was used to 'map' the information available to inform intervention and service delivery. Scholarly and grey literature written in English was identified in six databases, using a combination of keywords (e.g. guidelines, management, models and DCD); a 'snow-balling' technique was also used in Canada and the UK to access clinical protocols used in publicly funded health care systems. Over 500 documents were screened: 31 met inclusion criteria as they outlined practice principles for children with DCD as a population. Data regarding best practices were independently extracted by two reviewers and then compared with achieve consistency and consensus.
Results:
Two over-arching themes emerged, with five principles: (1) Organizing services to efficiently meet the comprehensive needs of children (e.g. Increasing awareness of DCD and coordination; Implementing clearly defined pathways; Using a graduated/staged approach); (2) Working collaboratively to offer evidence-based services (e.g. Integration of child and family views; Evidence-based interventions fostering function, participation and prevention).
Conclusion:
Numerous documents support each of the principles, reflecting agreement across studies about recommended organization of services. While these principles may apply to many populations of children with disabilities, this review highlights how essential these principles are in DCD. Researchers, managers, clinicians, community partners and families are encouraged to work together in designing, implementing and evaluating interventions that reflect these principles.
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