Abstract
Sleep problems are common in Rett syndrome and other neurogenetic syndromes. Actigraphy is a cost-effective, objective method for measuring sleep. Current guidelines require caregiver-reported bed and wake times to facilitate actigraphy data scoring. The current study examined missingness and consistency of caregiver-reported bed and wake times from paper sleep diaries and actigraphy event mark button presses in a sample of 38 individuals with Rett and related syndromes (aged 2–36 years, mean ¼ 13.1) across two 14-day collection time points. Rates of missingness and discrepancy between the 2 sources were relatively high and correlated with clinical severity and quality of life. Overall, the results suggest a need for alternative actigraphy scoring methods that do not rely on caregiver report in this population.
Original language | English (US) |
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Pages (from-to) | 1-12 |
Number of pages | 12 |
Journal | American journal on intellectual and developmental disabilities |
Volume | 130 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2025 |
Bibliographical note
Publisher Copyright:© 2025 American Association on Mental Retardation. All rights reserved.
Keywords
- Rett syndrome
- actigraphy
- parent burden
- sleep
PubMed: MeSH publication types
- Journal Article