2 research outputs found
Children and young people's experiences of living with developmental coordination disorder/dyspraxia: study protocol for a qualitative evidence synthesis
Children with developmental coordination disorder (DCD) face significant
challenges to deal with everyday activities due to underlying motor
proficiency difficulties. These challenges affect children and young people’s
participation; that is, involvement in daily life situations. In the past, limited
consideration was given to personal experience of events, relationships
and everyday life in children and young people with DCD; as a result,
understanding what it is like to live with DCD is not well conceptualised in
the literature. There is a pressing need to synthesise the findings of discrete
qualitative studies to advance the conceptual understanding of living with
DCD, to inform health service delivery and the development and
implementation of complex interventions. This study aims to systematically
review and synthesise qualitative literature regarding children and young
people’s experiences and views of everyday life and living with DCD. The
method of qualitative evidence synthesis that will be followed in this review
is a meta-ethnography. The eMERGe and PRISMA reporting guidelines will
be used in the development, design and reporting of this review. Nine
databases will be searched; Academic Search Complete, AMED, CINAHL,
MEDLINE, PsychArticles, PsychInfo, EMBASE, SPORTDiscus, and Web of
Science. Two independent reviewers will use the Joanna Briggs Institute
Checklist to appraise all included papers. The findings of this
meta-ethnography will endeavour to inform future research, policy and
practice. In particular, the results will help to inform the design of future
complex interventions to meet the needs of children and young people with
DCD. Dissemination will involve the publication of the results in a
peer-reviewed journal. Increasingly researchers and policymakers are
calling for services to be informed by the perspective and voice of children
with DCD; therefore, a policy brief will be published so that the findings are
widely available