Study of the Academic and Professional Course of Narcoleptic Patients (NARCOSCOL-NARCOVITAE)
1 other identifier
observational
1,605
1 country
18
Brief Summary
Narcolepsy is a chronic, disabling, and rare sleep disorder (prevalence 1/2500) characterized by excessive daytime sleepiness and, in some patients, falls in muscle tone related to emotions (cataplexies). It often begins in childhood or in young adults. Symptoms of narcolepsy are responsible for an important handicap in everyday life, and are often misunderstood by the family and professional environment. In addition, many comorbidities are associated with narcolepsy, such as depression, anxiety, or obesity. Few studies have investigated the impact of narcolepsy on patients' academic background, socio-professional integration, and quality of life. Narcoleptic patients may experience more difficulties in their academic and professional path than non-narcoleptic people. These difficulties would be multifactorial (related to the disease itself, comorbidities, external factors ...). As a better understanding of these determinants could help to inform patients and guide them in their choices, this study propose to establish a comprehensive inventory of educational and professional trajectories of narcoleptic patients in France in order assess the specificity of the difficulties encountered by the people concerned in their life course and to appreciate the attitude of the academic and professional circle with respect to the disease. This category 3 study (according to the French law "Loi Jardé") is based on the case-control model and will be conducted in all National Reference and Competence Centers for Narcolepsy and Hypersomnia. It will include a population of adult and paediatric patients. It will answer questions about work and schooling in these patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2020
Typical duration for all trials
18 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 4, 2018
CompletedFirst Posted
Study publicly available on registry
December 5, 2018
CompletedStudy Start
First participant enrolled
February 27, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 27, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 27, 2023
CompletedApril 18, 2023
April 1, 2023
3 years
December 4, 2018
April 14, 2023
Conditions
Outcome Measures
Primary Outcomes (2)
For adult : distribution of professional situations
Distribution of professional situations in narcoleptic adult patients and related non-narcoleptic topics (employed, unemployed, student, retired, housewife/husband). (data collection form "professional situation").
45 minutes (time to answering the questionnaire)
For children : proportion of children who repeated a grade
Proportion of children who repeated a grade in narcoleptic children and non-narcoleptic control children ("school status" data collection form).
45 minutes (time to answering the questionnaire)
Study Arms (4)
Adult Case Group
Adults with type 1 narcolepsy according to the ICSD3
Adult Control Group
Parents, cousins and / or friends of included narcoleptic adult patients, at least 18 years old and not suffering from narcolepsy.
Children Case Group
Children with type 1 narcolepsy according to the OCSD3
Children Control Group
Close friends and cousins of included narcoleptic children, minor and not suffering from narcolepsy.
Interventions
Patients and case control will have to respond to the study questionnaire on the online entry platform to compare the distribution of socio-professional categories. Answering the questionnaires will take 45 minutes.
Patients and case control will have to respond to the study questionnaire on the online entry platform to compare the proportion of subjects having repeated grades. Answering the questionnaires will take 45 minutes.
Eligibility Criteria
This study will focus on pediatric and adult patients with type 1 narcolepsy and followed up in one of the participating rare disease reference or competence centers. Two control banks will be constituted: 1. an "adult control" bank whose age is greater than 18 years: may be composed of the parents of included narcoleptic children or cousins and friends of included adult narcoleptic patients 2. a bank " child control' whose age is less than 18 years: may be composed of friends and cousins of included narcoleptic children.
You may qualify if:
- The case group:
- Children (6 years \<age \<18 years) or adults with type 1 narcolepsy diagnosed on:
- a clinic in favor of narcolepsy: excessive daytime sleepiness lasting for more than 3 months.
- cataplexy and an positive multiple sleep latency test (mean sleep latency ≤ 8 min and ≥ 2 SOREM) or a hypocretin dosage in the CSF \<110pg / L.
- Patients followed in one of the centers participating in the research.
- The control group:
- At least one person close to the case (cousins, close friends ...).
- For adults: same sex as the case and if possible same age (+/- 5 years).
- For minors: same sex and if possible same age (+/- 2 years).
- Person not suffering from narcolepsy.
You may not qualify if:
- The case group:
- Patients refusing to participate.
- Patients who do not speak the French language (incompatible with the reading, the comprehension and the filling of the questionnaires).
- Patients whose diagnosis of type 1 narcolepsy is not certain and / or has type 2 narcolepsy.
- Patients with narcolepsy symptomatic of another neurological disease.
- The group controls:
- Person refusing to participate.
- Person who does not speak French (incompatible with reading, understanding and filling out questionnaires).
- The brothers and sisters of the case cannot be witnesses of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (18)
Centre de médecine du Sommeil CHU d'Angers
Angers, 49033, France
Service d'Explorations Fonctionnelles du Système Nerveux, Clinique du Sommeil, CHU de Bordeaux Groupe Hospitalier Pellegrin
Bordeaux, 33076, France
Unité de sommeil pédiatrique - Hôpital femme Mère Enfant - Hospices civils de Lyon
Bron, 69677, France
Service de neurophysiologie clinique CHU de Dijon
Dijon, 21 079, France
Service de physiologie et Exploration fonctionnelle - Unité du Sommeil Hôpital Raymond Poincarré
Garches, 92 380, France
Service de Neurophysiologie Clinique, Hôpital Roger Salengro
Lille, 59037, France
Centre de Médecine du Sommeil et des Maladies respiratoires - Centre Hospitalier de la Croix Rousse - Hospices Civils de Lyon
Lyon, 69004, France
Service de neurophysiologie clinique - centre du sommeil - Hôpital de la Timone
Marseille, 13005, France
Service de Neurologie - Troubles du Sommeil Hôpital Gui de Chauliac
Montpellier, 34295, France
Laboratoire d'Explorations Fonctionnelles Neurologiques, CHU de Nantes
Nantes, 44 093, France
Centre du Sommeil et de la vigilance - Centre de référence Hypersomnies rares - Hôpital de l'Hôtel Dieu
Paris, 75 181, France
Service de Physiologie Explorations fonctionnelles Hôpital Bichat Claude Bernard
Paris, 75018, France
Service des pathologies du sommeil Hôpital Pitié-Salpêtrière
Paris, 75651, France
Centre pédiatrique des pathologies du sommeil APHP CHU Robert Debré - Paris
Paris, France
Service de Neurophysiologie Clinique et Centre du Sommeil, CHU de Poitiers
Poitiers, 86000, France
Centre des Troubles du Sommeil, Hospices Civils de Strasbourg
Strasbourg, 67 091, France
Explorations Neurophysiologiques, Hôpital Pierre Paul Riquet, CHU Toulouse Purpan
Toulouse, 31059, France
Centre du Sommeil du Service de Neurologie et de Neurophysiologie Clinique - CHRU Bretonneau
Tours, 37044, France
Related Publications (1)
Peter-Derex L, Fort E, Putois B, Martel N, Ricordeau F, Bastuji H, Arnulf I, Barateau L, Bourgin P, Dauvilliers Y, Debs R, Dodet P, Dudoignon B, Franco P, Hartley S, Lambert I, Lecendreux M, Leclair-Visonneau L, Leger D, Lemesle-Martin M, Leotard A, Leu-Semenescu S, Limousin N, Lopez R, Meslier N, Micoulaud-Franchi JA, Charley-Mocana C, d'Ortho MP, Philip P, Ruppert E, de La Tullaye S, Brigandet M, Margier J, Rolland B, Charbotel B, Mazza S. Effort/reward imbalance and comorbidities burden in academic and professional careers of patients with narcolepsy type 1. J Clin Sleep Med. 2025 Jun 1;21(6):983-997. doi: 10.5664/jcsm.11598.
PMID: 39943847DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 4, 2018
First Posted
December 5, 2018
Study Start
February 27, 2020
Primary Completion
February 27, 2023
Study Completion
February 27, 2023
Last Updated
April 18, 2023
Record last verified: 2023-04
Data Sharing
- IPD Sharing
- Will not share