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Updated: Jul 15, 2026

Multi-Modal Home Sleep Monitoring in Older Adults
Published on: January 26, 2019
Brief report: sleep in children with sickle cell disease: an analysis of daily diaries utilizing multilevel models
Cecelia R Valrie1, Karen M Gil, Rupa Redding-Lallinger
1The University of North Carolina at Chapel Hill, NC, USA. valriec@ecu.edu
Insights
Children with sickle cell disease (SCD) experience a bidirectional relationship between pain and sleep. Managing stress and pain medication use are crucial for improving sleep quality in pediatric SCD patients.
Area of Science:
- Pediatric Hematology
- Sleep Medicine
- Pain Management
Background:
- Sickle cell disease (SCD) is a chronic condition often associated with significant pain in children.
- The intricate relationship between pain and sleep in pediatric SCD is not fully understood.
- Understanding this dynamic is crucial for improving quality of life.
Purpose of the Study:
- To investigate the bidirectional relationship between daily pain and sleep quality in children with SCD.
- To examine the moderating effects of stress and pain medication on the pain-sleep connection.
- To inform clinical interventions for managing chronic pain in pediatric SCD.
Main Methods:
- A longitudinal study involving 20 children (aged 8-12) with SCD.
- Daily diary entries collected over up to 2 months, recording sleep, pain, stress, and medication use.
- Multilevel modeling used for data analysis to account for within-subject variability.
Main Results:
- Significant bidirectional association found: higher pain led to poorer sleep, and poorer sleep led to higher pain the next day.
- Increased stress was linked to reduced sleep duration.
- Same-day pain and pain medication intake appeared to lessen the negative impact of pain on sleep quality.
Conclusions:
- Sleep quality is a critical factor influencing daily functioning in children with SCD and chronic pain.
- Findings suggest that interventions targeting sleep hygiene and addressing sleep disturbances can aid in pain management for pediatric SCD.
- This knowledge empowers families and healthcare providers in managing SCD pain.
Objective:
To investigate the pain-sleep relationship in children with sickle cell disease (SCD) and the influence of stress and pain medication use on this relationship.
Method:
Children with SCD (n = 20; aged 8-12 years) completed daily diaries assessing sleep, pain, stress, and pain medication use for up to 2 months. Data analyzed using multilevel modeling.
Results:
High daily pain was related to poor sleep quality that night and poor sleep quality was related to high pain the following day. High stress was related to less sleep. High same-day pain and pain medication attenuated the impact of pain on sleep quality.
Conclusion:
Results highlight the importance of sleep in addressing functioning in children with chronic pain, knowledge which may help patients and their families better manage the child's pain. Behavioral pain interventions may be improved by the inclusion of strategies to encourage proper sleep hygiene and address sleep issues.
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