Recruiting NCT07544563

Phenotypic Exploration During Sensory Stimulation in an Acoustic Chamber

— Observational Epilepsy Anxiety Depression Anxiety Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to: Registry conditions: Epilepsy, Anxiety, Depression Anxiety Disorder. Basic parameters: from 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: France
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Exploration phénotypique en Contexte de Stimulations Sensorielles en Chambre Acoustique

Overview

An observational behavioural and neurophysiological study of the effects of controlled sensory stimulation (such as music, for example) on brain function

Primary outcome measures

Neuronal networks [Time frame: All along the study (8 years)]

Secondary outcome measures (3)

Psychologic outcome : anxiety [Time frame: 8 years]
Psychologic outcome 2 : depression [Time frame: 8 years]
Quality of life measure [Time frame: 8 years]

Eligibility criteria

Inclusion criteria

For patients : epilepsy
For healthy volunteers: age > 18 yo

Exclusion criteria

For patients and healthy volonteers : Deafness
For healthy volunteers : History of neurological conditions (including stroke, coma, epilepsy, neuro-inflammatory or neurodegenerative disease) or diagnosed cognitive impairment

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model: Cohort

Study locations

France · 1 center

GHU Paris Sainte Anne — Paris

Identifiers

NCT: NCT07544563 · D25-P008

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗