Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Completed NCT04570761

Effects of Auditory Brain Stimulation by "Pink Noise" on Memory Capacities in Alzheimer's Disease: Proof of Concept Study

Conditions: Alzheimer's Disease (AD)

Sex: All
Ages: 50 Years – N/A
Healthy volunteers: Yes
Phase: NA
Enrollment: 19
Sponsor: University Hospital, Tours

Location: University Hospital of Tours Tours

Summary

Alzheimer's disease (AD) is a neurodegenerative disorder affecting almost 6% of the world's population over the age of 65. This disease, in its most typical sporadic form, is characterized by an episodic memory impairment linked to a deficit in consolidation. Many studies indicate that sleep promotes this consolidation stage during the deep slow sleep stage by facilitating the transfer of information between the hippocampus and the neocortex. A method of acoustic brain stimulation at night by pink noises has been recently developed and has shown its effectiveness in strengthening memory consolidation in healthy volunteers. Actually, there is no study observing the effect of this new stimulation method on populations with neurodegenerative pathologies, in particular in AD for which this technique could potentially become a therapeutic option. The hypothesis is that of a strengthening of the memory consolidation capacities in subjects with AD as has been shown in healthy subjects.

Eligibility Criteria

Inclusion Criteria common to all participants: * Age\> 50 years at the inclusion * Patient with regular sleep patterns * Patient having given written consent * Patient affiliated to a social security regimen Inclusion criteria for subjects with Alzheimer's disease: * Patient with a beginning Alzheimer's disease defined according to the criteria of the National Institute on Aging-Alzheimer's Association or carriers of a prodromal Alzheimer's disease defined according to the criteria of the International Working Group IWG-2; the diagnosis must be supported by brain imaging and a blood test carried out in routine care * MMSE score ≥ 24 Inclusion criteria for healthy volunteers: * Absence of neurodegenerative pathologies * Matched in age (+/- 5 years) and in sex with a patient Non-inclusion criteria common to all participants: * Psychiatric pathologies (except depression or anxiety disorders stabilized for more than 3 months) * History of pathology which may have consequences on cognitive functioning and / or sleep: brain tumor, constituted stroke, epilepsy, head trauma (with clinical or parenchymal sequelae objectified on brain imagery), brain surgery * Any significant comorbidity likely to constitute a confounding factor according to the clinician * Psychotropic treatments introduced or modified \ 5 on the Pittsburg sleep quality index (PSQI) * A score\> 10 on the Epworth sleepiness index

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04570761). StuddyBuddy aggregates publicly available trial information.