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Characterization of Children with Complaints of Excessive Daytime Sleepiness

Characterization of Children with Complaints of Excessive Daytime Sleepiness

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06898008
Acronym
CEPSDE
Enrollment
400
Registered
2025-03-27
Start date
2024-01-01
Completion date
2024-10-31
Last updated
2025-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Excessive Daytime Sleepiness

Brief summary

10% of the population suffers from excessive daytime sleepiness. This can be explained by a variety of etiologies: psychiatric disorders, altered sleep quantity or quality, hypersomnia... The consequences on quality of life are not negligible, with emotional, academic, social, financial and somatic repercussions. Diagnosing and managing them is essential. This is the role of the HFME's Child Sleep Service, a reference center for rare narcolepsy and hypersomnia, which carries out a weekly hypersomnia assessment. In this context, the investigators are carrying out a retrospective descriptive study, the primary objective of which is to describe the results and diagnoses of hypersomnia check-ups in the HFME's Sleep Department, in order to obtain feedback on the center's activity and its evolution. The secondary objectives are to characterize the patients in the different diagnostic groups, to highlight factors associated with the different diagnoses, and to describe changes in patient characteristics over time.

Interventions

OTHERAssessment of socio-demographic, anthropometric, psychometric and clinical characteristics

age, sex and place of residence, socioeconomic level, education, anthropometric data, first-degree family history, screen time, physical activity time, sleep time, comorbidity, drug treatments, education, total IQ, results of Epworth, CDI, ISI, ADHD, CONNERS, SCSC, Horne and Ostberg questionnaires, hearing aids, referring professional, melatonin dosage, ferritinemia, etiology of sleepiness

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years

Inclusion criteria

* \- Patient hospitalized in the HFME sleep department for a diagnostic assessment of hypersomnia. * Age under 18 at the time of hospitalization * From January 2015 to December 2023

Exclusion criteria

* \- No balance sheet * Age over 18 at time of hospitalization * Assessment for medicolegal or therapeutic adaptation purposes

Design outcomes

Primary

MeasureTime frame
Describe the results and diagnoses of hypersomnia assessments in the HFME Sleep DepartmentFeedback consultation 1 month after inpatient assessment

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026