Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05773872

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surveillance

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

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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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