Childhood ABI Fatigue Physiological Marker Study
Research type
Research Study
Full title
Fatigue after acquired brain injury in children: physiological marker development study
IRAS ID
268831
Contact name
Ram Kumar
Contact email
Sponsor organisation
Alder Hey Children's NHS FT
Duration of Study in the UK
1 years, 0 months, 0 days
Research summary
Childhood acquired brain injury (ABI) is frequent affecting at least 300 per 100,000 children per year worldwide, often resulting in chronic disability. Fatigue is a common “hidden” disability after ABI affecting physical, cognitive, emotional and societal function in up to 75% of survivors. Clinical fatigue is incompletely understood at a pathophysiological level and often missed in clinics since it is invisible, difficult to measure, fluctuates, and relies on subjective report often by carers rather than the child. Quantitative neurophysiological markers of fatigue or related psychophysiological impairments are described in adults with ABI, but not used widely in clinical practice due to practical constraints; and not described in relation to fatigue in children. Developing reliable and valid neurophysiological markers of fatigue in children with ABI, which are low-cost and feasible to apply in routine clinical settings would aid treatment of fatigue and thus improve outcomes.
The aim of this development study is to develop methods to identify candidate electrophysiological biomarkers of clinical fatigue in children with an acquired brain injury (ABI), which are feasible to apply in routine clinical settings. We will use CE-marked wearable technology for capturing EEG and peripheral autonomic system (heart rate, skin conductance) signals as potential biomarkers of fatigue in children suffering ABI-related fatigue and controls without. The signals will be recorded at rest and during a battery of cognitive tasks, which we will develop based on cognitive tasks in routine clinical use by clinicians treating children after ABI or those used previously in the experimental psychology studies in children which have not as yet entered routine clinical practice. We will optimise signal acquisition and characterise performance in the children against available standard methods.REC name
North West - Liverpool Central Research Ethics Committee
REC reference
20/NW/0060
Date of REC Opinion
26 May 2020
REC opinion
Further Information Favourable Opinion