Examination of Sleep and Family Functioning in Pediatric Craniopharyngioma Patients

Completed

Conditions studied: Craniopharyngioma

In brief

Pediatric craniopharyngioma patients experience significant endocrine and sleep dysregulation difficulties. Sleep is a crucial part of children's healthy development, and sleep difficulties are associated with severe functional morbidity. Insufficient sleep, excessive daytime sleepiness, and poor sleep quality have all been significantly related to academic, behavioral, and emotional functioning in children and adolescents. Ecological momentary assessments (EMA) will be used to collect observational data. EMA data will be collected twice daily for one week. For the morning EMA administration, participants will be asked about their sleep. During the evening administration, participants will be asked about their daytime sleepiness, overall well-being, and family functioning. Covariates also administered during the evening administration include medication administration (Y/N) and total screen time. At the end of the EMA data collection period (on day 7 OR 8), participants will be sent a survey asking them to report - anonymously - their overall experience and satisfaction with the EMA data collection method.

Key facts

Study ID

NCT03330080

Run by

St. Jude Children's Research Hospital

People needed

41

Starts

2018-02-12

Expected to finish

2019-01-29

Last updated by the study team

2019-03-08

Who can join

Age: 8 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Craniopharyngioma diagnosis
• Access to smartphone or a tablet
• Agreement to download Ilumivu application
• The ability for the participant to answer questionnaires (i.e., no cognitive or developmental diagnoses that would preclude understanding and completing child self-report questionnaires)
• Age between 8 and 18 years old at the time of enrollment onto St. Jude protocol RT2CR.
• Participated in sleep study component of RT2CR

You may not qualify if…

• Limited English proficiency as evidenced by an inability to read and respond to EMA survey questions
• Visual or sensorimotor impairment (e.g., loss of sight)

Where it is running

• St . Jude Children's Research Hospital — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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