Actively Recruiting

Early Phase 1
Age: 55Years +
All Genders
Healthy Volunteers
ID06002477

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

Age: 55Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Anticholinergic Challenge

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

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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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