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NCT03330080 · ClinicalTrials.gov registry record

Examination of Sleep and Family Functioning in Pediatric Craniopharyngioma Patients

A clinical trial of Craniopharyngioma, sponsored by St. Jude Children's Research Hospital.

Completed
Registry status
41
Enrollment target
1
Study location

NCT03330080 is a study of Craniopharyngioma that has completed, run by St. Jude Children's Research Hospital. The registered enrollment target is 41 participants, below the 209-participant average among 6 other Craniopharyngioma trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03330080, a study of Craniopharyngioma, has completed, sponsored by St. Jude Children's Research Hospital.

COMPLETED
Registry status
41 participants
Enrollment target
1
Study location

Study Summary

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.

Conditions Studied

Study Locations (1)

Tennessee

  • St . Jude Children's Research Hospital - Memphis

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2018-02-12
Est. Completion 2019-01-29

What the Registry Record Tells You About NCT03330080

The ClinicalTrials.gov registry entry for NCT03330080 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 209-participant average among 6 other Craniopharyngioma trials with a reported enrollment target (80% lower). The listed sponsor is St. Jude Children's Research Hospital, which has 410 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Craniopharyngioma appearing as the primary indexed condition, and to 0 interventions.

NCT03330080 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.

Frequently Asked Questions

What is clinical trial NCT03330080 about?

NCT03330080 is a clinical study titled "Examination of Sleep and Family Functioning in Pediatric Craniopharyngioma Patients". 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 sl...

What is the current status of trial NCT03330080?

This trial is currently completed. The enrollment target is 41 participants. The study started on 2018-02-12. Estimated completion is 2019-01-29.

What conditions does trial NCT03330080 study?

This clinical trial studies the following conditions: Craniopharyngioma.

Who is sponsoring clinical trial NCT03330080?

This trial is sponsored by St. Jude Children's Research Hospital, which has 410 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03330080 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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