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Search / Trial NCT05708001

Improvement of Memory in Mild Cognitive Impairment

Launched by LUCIE BRÉCHET · Jan 22, 2023

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Autobiographical Memory (Abm) Memory And Cognition Transcranial Alternating Current Stimulation (T Acs) High Density Electroencephalography (Hd Eeg)

ClinConnect Summary

This clinical trial is studying a treatment called transcranial alternating current stimulation (tACS) to see if it can help improve memory in older adults who have mild cognitive impairment (MCI). MCI is a condition where people experience more memory problems than expected for their age, but it is not severe enough to be classified as dementia. The trial will involve caregivers leading the tACS sessions remotely, and researchers want to find out if this repeated treatment can lead to lasting improvements in memory and brain activity.

To participate, individuals must be at least 55 years old, have a diagnosis of mild cognitive impairment confirmed by a healthcare professional, and be able to understand and sign the consent form. Caregivers who help with the treatment must be at least 21 years old and comfortable using a computer or tablet. Participants can expect to engage in regular tACS sessions, which are non-invasive and aim to enhance memory function. It's important to note that certain health conditions may exclude individuals from participating, so a thorough screening will be conducted to ensure safety. If you or someone you know is interested, it could be a valuable opportunity to contribute to research aimed at improving memory health in older adults.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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
  • Exclusion Criteria:
  • Mild Cognitive Impairment (MCI) patients
  • age \< 55 years old
  • any current diagnosis of a psychiatric disorder (e.g., schizophrenia, bipolar disorder, 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
  • history of head trauma resulting in prolonged loss of consciousness
  • current history of poorly controlled headaches including chronic medication for migraine prevention
  • history of fainting spells of unknown or undetermined etiology that might constitute seizures
  • history of seizures, diagnosis of epilepsy
  • any unstable medical condition or chronic uncontrolled medical conditions that may cause a medical emergency in case of a provoked seizure (cardiac malformation, cardiac dysrhythmia, asthma, etc.)
  • contraindication for undergoing MRI or receiving tACS
  • 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)
  • any skin problems, such as dermatitis, psoriasis, or eczema
  • any electrically, magnetically, or mechanically activated implanted devices such as a pacemaker, intracranial electrodes, implanted defibrillators, medication pumps, nerve stimulators, vascular clips, or any other prosthesis in the brain
  • any serious life-threatening disease such as congestive heart failure, pulmonary obstructive chronic disease, or active neoplasia
  • pregnant women
  • adults lacking capacity for consent
  • Caregiver
  • insufficient understanding of study procedures
  • poor eyesight, severe arthritis in the hands, pain, deformity or other condition that interferes with successful administration of tACS

About Lucie Bréchet

Lucie Bréchet is a clinical trial sponsor dedicated to advancing medical research through rigorous and ethically conducted studies. With a focus on innovation and patient-centered outcomes, the sponsor supports the development of novel therapies and interventions aimed at improving health and quality of life. Committed to upholding the highest standards of scientific integrity and regulatory compliance, Lucie Bréchet collaborates with multidisciplinary teams to drive impactful clinical research across various therapeutic areas.

Locations

Geneva, , Switzerland

Patients applied

0 patients applied

Trial Officials

Lucie Bréchet, PhD

Principal Investigator

University of Geneva (UNIGE)

Paul G Unschuld, PhD

Study Chair

Geneva University Hospitals (HUG)

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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