Senior Research Officer
BSc (Hons), PhD
Dr Jacinta Saldaris is an early career researcher, graduating from The University of Western Australia School of Human Sciences with a Doctor of Philosophy (2020). She is a Senior Research Officer in the Child Disability Team for the International CDKL5 Clinical Research Network (ICCRN), an NIH-funded project that comprises a collaboration with the University of Colorado, the Children’s Hospital of Philadelphia and CDKL5 Centre of Excellence Clinics. The project aims to develop and validate a suite of outcome measures to be used in disease modifying clinical trials for children with CDKL5 deficiency disorder (CDD) and other Developmental Epileptic Encephalopathies (DEEs). This work is essential for strong clinical trials for rare disorders and is making a critical contribution to ensuring excellent evaluations of promising therapies on the horizon.
Jacinta’s research experience includes rare disorders, neurodevelopmental disorders, physical activity and exercise, and mental health. Her research envisions that children with disability and their families live with better health and quality of life, generating high impact research through a collaborative approach. Jacinta has presented her research at multiple conferences, most recently being the 2022 American Epilepsy Society Conference held in Nashville. She received the 2022 Loulou Foundation Junior Fellowship Award for her work with CDD and was a finalist for the Young Investigator Award for the Exercise and Sports Science Australia Research to Practice Conference in 2021.
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Publications
February 2024
Communication of individuals with CDKL5 deficiency disorder as observed by caregivers: A descriptive qualitative study
CDKL5 deficiency disorder (CDD) is a genetically caused developmental epileptic encephalopathy that causes severe communication impairments. Communication of individuals with CDD is not well understood in the literature and currently available measures are not well validated in this population. Accurate and sensitive measurement of the communication of individuals with CDD is important for understanding this condition, clinical practice, and upcoming interventional trials.
Published research Language Development Child Disability Child disabilityJanuary 2024Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric study
Validated measures capable of demonstrating meaningful interventional change in the CDKL5 deficiency disorder (CDD) are lacking. The study objective was to modify the Rett Syndrome Gross Motor Scale (RSGMS) and evaluate its psychometric properties for individuals with CDD.
Published research Rett Syndrome Child Disability Child disabilitySeptember 2023The development, content and response process validation of a caregiver-reported severity measure for CDKL5 deficiency disorder
CDKL5 Deficiency Disorder (CDD) is a severe X-linked developmental and epileptic encephalopathy. Existing developmental outcome measures have floor effects and cannot capture incremental changes in symptoms. We modified the caregiver portion of a CDD clinical severity assessment (CCSA) and assessed content and response-process validity.
Published research Child Disability Child disabilityMay 2023Validating the Communication and Symbolic Behavior Scales–Developmental Profile Infant–Toddler Checklist (CSBS–DP ITC) Beyond Infancy in the CDKL5 Deficiency Disorder
CDKL5 deficiency disorder (CDD) results in early-onset epilepsy and lifelong cognitive and motor impairments. With no validated measure for communication in CDD, this study evaluated the psychometric properties of the Communication and Symbolic Behavior Scales-Developmental Profile Infant Toddler Checklist.
Published research Child Disability Child disability -
Education and Qualifications
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Awards/Honours