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Clinical Trials/NCT05710549
NCT05710549
Recruiting
Not Applicable

Understanding Brain Mechanisms Involved in Autobiographical Memory Using High-density Electroencephalography and Transcranial Alternating Current Stimulation

Lucie Bréchet1 site in 1 country120 target enrollmentApril 25, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mild Cognitive Impairment
Sponsor
Lucie Bréchet
Enrollment
120
Locations
1
Primary Endpoint
Spatiotemporal dynamic changes measured with electroencephalography (hdEEG)
Status
Recruiting
Last Updated
9 months ago

Overview

Brief Summary

The overall objective of this project is to characterize the spatiotemporal dynamics of brain oscillations underpinning autobiographical memory (ABM) and the modulation of the memory network using non-invasive brain stimulation.

Detailed Description

Accumulating evidence suggests that activity in distributed networks supporting ABM is altered even decades before the expected onset of clinical symptoms in Alzheimer's disease (AD). Robust network alterations associated with age-related memory and cognitive decline have been linked to abnormal oscillatory brain rhythmic activity and functional dysconnectivity. However, the detailed neural mechanisms are still poorly understood. The investigators propose to precisely characterize the underlying neurophysiological mechanisms that lead to behavioral and cognitive disturbances in ABM of MCI patients. Specifically, hdEEG will be used to characterize the sources and spatiotemporal dynamics of the neuronal activity involved in the ABM network of 40 mild cognitive impairment (MCI) patients and compare it to 40 age-matched, older healthy participants and 40 healthy young participants. The investigators will then apply non-invasive brain stimulation in the form of transcranial alternating current stimulation (tACS) to gain novel insights into the causal role of brain oscillations in the ABM network of MCI patients.

Registry
clinicaltrials.gov
Start Date
April 25, 2022
End Date
August 1, 2027
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Lucie Bréchet
Responsible Party
Sponsor Investigator
Principal Investigator

Lucie Bréchet

Dr.

University of Geneva, Switzerland

Eligibility Criteria

Inclusion Criteria

  • Cognitively-Unimpaired Younger and Older Adults
  • Age 18 to 35 years old (younger adults)
  • Age 55+ years old (older adults)
  • without any cognitive impairment (based on the Montreal Cognitive Assessment: MoCA)
  • willing and capable to give informed consent for participation in the study after it has been thoroughly explained able
  • willing to comply with all study requirements informed consent form was signed
  • Mild Cognitive Impairment (MCI) patients
  • Age 55+ years old
  • Clinical Diagnosis of MCI
  • Confirmation of diagnosis will be made by the study MD based on a holistic consideration of the participant's cognitive evaluation and history

Exclusion Criteria

  • Cognitively-Unimpaired Younger and Older Adults
  • any cognitive impairment captured by the Montreal Cognitive Assessment (MoCA) - score \< 26
  • major psychiatric co-morbidity including major depressive disorder, schizophrenia, or psychosis
  • blindness or other disabilities that prevent task performance
  • Contraindication for undergoing MRI
  • Any metal in the brain or skull (excluding dental fillings) or elsewhere in the body unless cleared by the responsible covering MD (e.g. MRI compatible joint replacement)
  • Mild Cognitive Impairment (MCI) patients
  • Age \< 55 years old
  • Any current diagnosis of a major psychiatric disorder (e.g., schizophrenia, bipolar disorder, major depressive disorder)
  • Other than MCI, any history of other progressive or genetic neurologic disorder (e.g. Parkinson's disease, multiple sclerosis, tubular sclerosis) or acquired neurological disease (e.g. stroke, traumatic brain injury, tumor), including intracranial lesions

Outcomes

Primary Outcomes

Spatiotemporal dynamic changes measured with electroencephalography (hdEEG)

Time Frame: up to 30 minutes

Changes in spatiotemporal dynamics in different frequency bands (theta, alpha, beta, gamma) will be assessed with hdEEG

Cognitive Assessment

Time Frame: baseline

The Montreal Cognitive Assessment (MOCA) will be administered to characterize the cognitive status

Study Sites (1)

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