Actively Recruiting
Evaluation of Social Cognition in Patients With Type 1 or Type 2 Narcolepsy Compared to Patients With Idiopathic Hypersomnia
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2026-06-01
75
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate social cognition and related cognitive functions in adults diagnosed with type 1 or type 2 narcolepsy or idiopathic hypersomnia. Narcolepsy is a chronic neurological disorder characterized by excessive daytime sleepiness, with type 1 linked to hypocretin deficiency and cataplexy symptoms, and type 2 showing normal hypocretin levels without cataplexy. The study addresses the impact of narcolepsy on social cognition, mood, attention, and decision-making, areas that have not been extensively studied, especially with control groups for comparison. Participants will be randomized into three groups: type 1 narcolepsy, type 2 narcolepsy, and idiopathic hypersomnia. Each participant will undergo psychometric evaluation through validated questionnaires assessing social cognition and cognitive functions. The questionnaires include the Sustained Attention to Response Task (SART), Iowa Gambling Task (IGT), Impulsive Behaviour Scale (UPPS), Toronto Alexithymia Scale (TAS), Basic Empathy Scale (BES), Facial Emotions Recognition Task (FRET), ERF-CS, and the Movie for the Assessment of Social Cognition (MASC). During the two-year study period, participants will complete these assessments alongside their usual care. Researchers will measure mean scores on the SART, IGT, and UPPS across the three groups to understand cognitive and social cognition differences. The study is triple-masked and randomized, with careful monitoring of participant responses to these questionnaires to explore social and cognitive aspects of these sleep disorders.
CONDITIONS
Brief Title
Evaluation of Social Cognition in Patient With Type 1 or Type 2 Narcolepsy Versus Patients With Idiopathic Hypersomnia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 years or older
- Diagnosed with type 1 or type 2 narcolepsy or idiopathic hypersomnia
- No opposition to participate
You will not qualify if you...
- Presence of other psychiatric or neurological diseases
- Under 18 years old
- Under guardianship, curatorship, or deprived of liberty
- Refusal to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 2 years
Participants complete validated questionnaires assessing social cognition in addition to their usual care.
Questionnaire assessments over 2 years
Trial Site Locations
Total: 1 location
1
CHU Amiens-Picardie
Amiens, France, 80054
Actively Recruiting
Research Team
M
Mathilde FLAMAND, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
3
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