Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07544563

Phenotypic Exploration During Sensory Stimulation in an Acoustic Chamber

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

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Epilepsy Anxiety Anxiety Disorders Brain Diseases Central Nervous System Diseases Depression Anxiety Disorder Mental Disorders Nervous System Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

GHU Paris Sainte Anne

Paris, 75014, France

Location status: Recruiting

Location contact

Estelle Pruvost-Robieux, MD, PHD

CONTACT

[email protected]

+33145658189

Estelle Pruvost-Robieux, MD, PHD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Neuronal networks

    Time frame: All along the study (8 years)

    Description of the neural networks involved during exposure to sensory stimuli

Secondary outcomes

  1. Psychologic outcome : anxiety

    Time frame: 8 years

    Assessment of the Generalized Anxiety Disorder-7 (GAD7) in the exposed patients across the hospitalization :

    minimum value 0; maximum 21; higher scores mean a worse outcome

  2. Psychologic outcome 2 : depression

    Time frame: 8 years

    Assessment of the Neurological Disorders Depression Inventory for Epilepsy (NDDI-E) in the exposed patients across the hospitalization : minimum value 6; maximum 24; higher scores mean a worse outcome

  3. Quality of life measure

    Time frame: 8 years

    Assessment of the QOLIE-31(quality of life in epilepsy) scale among exposed patients

Study contacts

Contact information is provided by the study sponsor or research team.

Viviane AWASSI

CONTACT

[email protected]

+33145658486

Sponsors and collaborators

Lead sponsor

Centre Hospitalier St Anne

Other

Registry information

Official study title

Exploration phénotypique en Contexte de Stimulations Sensorielles en Chambre Acoustique

Acronym: EMO-INTRA

Important dates

Study start
2025
Primary completion
2035
Study completion
2035
First posted
Apr 22, 2026
Registry last updated
Apr 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.