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March 1, 2024Frontiers in Pediatrics2 citationsOpen Access

Referent data for investigations of upper limb accelerometry: harmonized data from three cohorts of typically-developing children

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CLCatherine E. LangCHCatherine R. HoytJKJeffrey D. Konrad

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Abstract

Aim The rise of wearable sensing technology shows promise for addressing the challenges of measuring motor behavior in pediatric populations. The current pediatric wearable sensing literature is highly variable with respect to the number of sensors used, sensor placement, wearing time, and how data extracted from the sensors are analyzed. Many studies derive conceptually similar variables via different calculation methods, making it hard to compare across studies and clinical populations. In hopes of moving the field forward, this report provides referent upper limb wearable sensor data from accelerometers on 25 variables in typically-developing children, ages 3–17 years. Methods This is a secondary analysis of data from three pediatric cohorts of children 3–17 years of age. Participants ( n = 222) in the cohorts wore bilateral wrist accelerometers for 2–4 days for a total of 622 recording days. Accelerometer data were reprocessed to compute 25 variables that quantified upper limb movement duration, intensity, symmetry, and complexity. Analyses examined the influence of hand dominance, age, gender, reliability, day-to-day stability, and the relationships between variables. Results The majority of variables were similar on the dominant and non-dominant sides, declined slightly with age, and were not different between boys and girls. ICC values were moderate to excellent. Variation within individuals across days generally ranged from 3% to 32%. A web-based R shiny object is available for data viewing. Interpretation With the use of wearable movement sensors increasing rapidly, these data provide key, referent information for researchers as they design studies, and analyze and interpret data from neurodevelopmental and other pediatric clinical populations. These data may be of particularly high value for pediatric rare diseases.

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Lang et al. (2024) studied this question.

synapsesocial.com/papers/68e76495b6db6435876da008https://doi.org/10.3389/fped.2024.1361757
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