Improvement of Memory in Mild Cognitive Impairment (MCI) Using Transcranial Alternating Current Stimulation (tACS) Guided by EEG and MRI: a Randomized, Sham-controlled, Parallel-arm, Double-blind Study

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The Clinical Trial will systematically examine the feasibility of remote, caregiver-led tACS for older adults with memory deficits and evaluate whether repeated tACS leads to sustained improvement of neuronal activity and memory functions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Maximum Age: 85
Healthy Volunteers: t
View:

⁃ Mild Cognitive Impairment (MCI) patients

• age ≥ 55 years old

• clinical diagnosis of mild cognitive impairment (MCI) based on a comprehensive clinical assessment and standard neuropsychological examination including tests of language, visuospatial thinking, executive functions, and memory

• confirmation of diagnosis will be made by Prof. Paul Unschuld, the study MD, based on a participant's cognitive evaluation and history

• understanding of the informed consent

• able and willing to comply with all study requirements

• informed consent form was signed

• women of childbearing potential (WOCBP) must perform a pregnancy test during screening

⁃ Caregiver

• minimum 21 years of age

• self-reported computer/tablet proficiency

• willingness to learn how to use tACS

• availability during the study period to administer tACS to the participant

• informed consent form was signed

• women of childbearing potential (WOCBP) must perform a pregnancy test during screening

Locations
Other Locations
Switzerland
University of Geneva, Campus Biotech
RECRUITING
Geneva
Contact Information
Primary
Lucie Bréchet, PhD
lucie.brechet@unige.ch
+41 22 379 08 52
Time Frame
Start Date: 2023-02-01
Estimated Completion Date: 2027-12-01
Participants
Target number of participants: 40
Treatments
Experimental: Transcranial alternating current stimulation (tACS)
The randomized, sham-controlled, parallel-arm, double-blind clinical trial will include 4 weeks of daily, home-based stimulation sessions. MCI patients will be randomly assigned to the active or sham group.
Experimental: neurophysiological (hdEEG)
At the baseline and after 4 weeks, MCI patients will be evaluated in the laboratory using hdEEG.
Experimental: clinical measures (MoCA)
At the baseline and after 4 weeks, MCI patients will be evaluated in the laboratory using MoCA.
Related Therapeutic Areas
Sponsors
Leads: Lucie Bréchet

This content was sourced from clinicaltrials.gov