Actively Recruiting
Attentional Mechanisms of Cognitive Compensation in Subjective Cognitive Decline
Led by Vanderbilt University Medical Center · Updated on 2026-06-04
80
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how attention networks function in older adults with subjective cognitive decline (SCD) by using an anticholinergic drug challenge and EEG. The study aims to understand whether SCD is linked to increased compensatory attention activity supported by cholinergic function and how disrupting this with the drug affects attention and brain activity. The trial focuses on cognitively normal older adults aged 55 and above, comparing responses under drug and placebo conditions. Participants will attend two visits where they receive either a 20 mg oral dose of mecamylamine, an anticholinergic drug, or a placebo in a randomized, double-blind order. During each visit, cognitive testing and EEG recording will be performed. The EEG uses a 128-channel sensor net to measure brain activity during tasks assessing different attention networks. Cognitive tests include the Attention Network Test, incidental memory tasks, and assessments of memory and psychomotor speed, all conducted under both drug and placebo conditions. Throughout the study, participants will undergo screening for cognitive status and psychiatric symptoms to ensure eligibility. Vital signs, ECG, and blood tests will be collected. Researchers will measure attention network function and brain responses using EEG and cognitive test outcomes. The primary outcome is the peak P1 amplitude in EEG after drug administration. The study will last across the two challenge visits, and all procedures are designed to monitor effects and maintain participant safety during and after drug administration.
CONDITIONS
Brief Title
Attentional Mechanisms in SCD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 55 years or older
- Montreal Cognitive Assessment (MoCA) score greater than 25
- Global Deterioration Scale (GDS) rating less than 3
- Non-smokers
You will not qualify if you...
- Medical conditions that prevent safe use of the study drug
- Diagnosed primary neurological disorders such as stroke or epilepsy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 study visits over approximately 1 week
Participants receive two randomized, double-blinded oral drug challenge visits, one with mecamylamine and one with placebo. Each visit includes cognitive testing and an electroencephalography (EEG) session to assess attentional network function.
2 visits (in-person) with drug administration and cognitive testing
Trial Site Locations
Total: 1 location
1
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37212
Actively Recruiting
Research Team
K
Kimberly Albert, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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