CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 152 enrolled
Drug / intervention
PET Biomarker Disclosurebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04818255
NCT04818255N/ACompleted

Stimulation to Improve Memory: PET Education & Disclosure

University of Michigan·interventional·Posted Mar 26, 2021·Updated Jan 29, 2026

In Brief

A clinical study evaluating PET Biomarker Disclosure for Mild Cognitive Impairment and Dementia; Alzheimer's Type (Etiology). Completed, enrolled 152 participants across 1 site.

Detailed Summary

When dementia is caused by AD, we refer to it as dementia of the Alzheimer's Type (DAT). The greatest risk factor for Alzheimer's Disease (AD) and DAT is advancing age, but DAT is not a normal part of aging. Studies have shown that changes in the brain happen before full symptoms of DAT develop. These changes include a buildup of two proteins within the brain, called amyloid and tau. The two goals of this study are (1) to determine whether patients with mild cognitive impairment or dementia-Alzheimer's type (DAT) are able to demonstrate decisional capacity to engage in PET amyloid and tau disclosure after receiving education; and (2) to assess how patients and care partners react to PET amyloid and tau biomarker disclosure.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedMar 26, 2021
Enrollment StartDec 10, 2020
Primary CompletionNov 7, 2024
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 5.3 years ago

Interventions

PET Biomarker Disclosurebehavioral

Participants receive information about whether they currently have elevated or not-elevated amyloid and/or tau based on recent PET imaging conducted as part of an affiliated research study (no additional imaging is required for this project). Participants meet with a licensed clinical neuropsychologist to discuss their biomarker status, the meaning of this information, and potential next steps to consider based of their status. Participants receive written summaries of this information, as well as resources as deemed necessary or as requested.