Development of a Software Correlating Simultaneously fMRI, EEG &

Clinical Trial Summary

The study aim to improve the quality of EEG recordings during simultaneous fMRI acquisitions. The second aim is to validate the correspondence between cerebral areas activated in fMRI and cortical areas identified with high density EEG during the listening of emotional musical pieces.

See also
	Status	Clinical Trial	Phase
	Completed	`NCT06032897` - Impact of Individualized Music Listening for People With Dementia on Anxiety: A Quasi-experimental Study	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT06032897 - Impact of Individualized Music Listening for People With Dementia on Anxiety: A Quasi-experimental Study

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03753620
Study type	Interventional
Source	Centre Hospitalier Universitaire de Besancon
Contact
Status	Completed
Phase	N/A
Start date	May 15, 2019
Completion date	March 1, 2022

Development of a Software Correlating Simultaneously fMRI, EEG and Peripheral Physiological Activity — NEUREXPLO

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms