Closed-Loop Brain Stimulation as a Potential Intervention for Cognitive Decline

Part of paid clinical trials in Austin, Texas.

Sponsor
University of Texas at Austin
Study ID
NCT05907343
Status
Recruiting

Conditions

  • Alzheimer Dementia (AD)
  • Mild Cognitive Impairment

Eligibility Criteria

Sex
ALL
Age
18 Years - 90 Years
Healthy Volunteers
Accepted

Interventions

  • Closed-loop TBS — DEVICE
    A BCI records and analyzes the participant's EEG as they perform cognitively demanding video game tasks. The BCI delivers TBS with a real coil when its output indicates that the participant is not properly engaged in the video game.
  • Open-loop TBS — DEVICE
    A BCI records and analyzes the participant's EEG as they perform cognitively demanding video game tasks. TBS with the real coil is delivered irrelevant of the BCI decoder output.

Study Details

The goal of this clinical study is to investigate the effectiveness of non-invasive stimulation to enhance cognitive control abilities in older adults with and without cognitive impairment. The main questions it aims to answer are: * whether it is possible to restore various cognitive functions in older adults by delivering theta burst stimulation (TBS), a form of transcranial magnetic stimulation, and * whether closed-loop TBS is able to induce therapeutic benefits that outperform open-loop TBS. Participants play a cognitive video game while a brain-computer interface (BCI) analyzes their electroencephalogram (EEG) signals and decodes the presence or absence of the contingent negative variation (CNV) potential, a marker of cognitive control. The BCI triggers TBS when its outputs indicate that the participant is not engaged properly in the video game. Researchers will compare the effects of closed-loop and open-loop TBS using the outcome metrics described below to see how much cognitive restorations is achievable with each stimulation modality.

Key Dates

First listed
Jun 18, 2023
Start date
May 31, 2023
Status verified
Aug 2026
Primary completion
Oct 31, 2027
Completion
Oct 31, 2027

Study Design

Enrollment
180 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Closed-Loop TBS
  • Active Comparator: Open-Loop TBS

Primary Outcome Measure

Cognitive Assessment Batteries [ Time Frame: Up to 8 weeks after intervention ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Health Discovery BuildingAustinTexas78712
Patrick Escamilla
512-495-5246

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