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Search / Trial NCT05998031

A Mechanistic Study to Investigate tDCS and Working Memory in MCI Patients

Launched by UNIVERSITY OF FLORIDA · Aug 16, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Cognitive Aging Brain Stimulation Functional Mri Computational Modeling Finite Element Method (Fem)

ClinConnect Summary

The AIM Pilot Study is a research project designed to explore how a treatment called transcranial direct current stimulation (tDCS) can help improve working memory in older adults who have mild cognitive impairment (MCI). This study is looking for participants aged 60 to 95 who have a certain level of cognitive ability, as measured by a simple test. If you or someone you know fits this age range and has a MoCA score of 18 or higher, you might be eligible to take part.

Participants will receive tDCS, which involves a gentle electrical stimulation to the scalp, and will take part in training sessions to help with the study. It’s important to note that there are some health conditions and devices (like certain implants) that would prevent someone from participating. The study is currently recruiting, so if you are interested, it could be a chance to contribute to our understanding of cognitive health in older adults.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Age 60-95 years
  • Montreal Cognitive Assessment (MoCA) score 18 and above (scores will be adjusted for education)
  • Able to receive electrical stimulation
  • Ability to comprehend conversational voices
  • Adequate motor capacity to operate computer mouse and click-button in-scanner
  • Ability to participate in the intervention and attend training sessions Exclusion Criteria
  • Failure to provide informed consent
  • Contraindications to MRI recording (e.g., any kind of ferrous metallic stents or ferrous metal objects in the body, heart valve prosthesis, or other metal implants, claustrophobia, neurostimulation system, defibrillator, pacemaker, or other implanted device)
  • Left-handed, or left hand dominant
  • History of neurological, seizures, and psychiatric disorders, traumatic brain injury, incidence of stroke involving large vessel
  • Terminal illness with life expectancy less than 12 months, as determined by physician
  • Brain tumor or malformation or any foreign body known or previously identified in brain
  • Cancer in active treatment, besides skin cancer
  • Currently on GABAergic or glutamatergic medications, or on calcium or sodium channel blockers, which alter or block the ability of tDCS to facilitate tissue excitability
  • Unable to communicate because of severe hearing loss or speech disorder
  • Severe sensory impairment
  • Inability to communicate in English
  • Severe visual impairment, which would preclude completion of the assessment and/or intervention
  • No physical impairment precluding motor response or lying still for an hour in the scanner that could confound study findings
  • Moderate-to-severe depressive symptoms as defined by scoring 10 or above on the Geriatric Depression Scale (GDS)

About University Of Florida

The University of Florida, a leading research institution, is dedicated to advancing healthcare through innovative clinical trials. With a focus on enhancing patient outcomes and exploring new therapeutic avenues, the university leverages its extensive resources, interdisciplinary expertise, and state-of-the-art facilities to conduct rigorous research across a variety of medical fields. Committed to ethical standards and patient safety, the University of Florida fosters collaboration among researchers, healthcare professionals, and community stakeholders to translate scientific discoveries into impactful clinical applications.

Locations

Gainesville, Florida, United States

Patients applied

0 patients applied

Trial Officials

Aprinda I Queen, PhD

Principal Investigator

University of Florida

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported