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Not Yet RecruitingNCT07243600

Improving Neurological Health With Acetylcholine Via Neuroplasticity-based Computerized Exercise in Mild Cognitive Impairment

Improving Neurological Health With Acetylcholine Via Neuroplasticity-based Computerized Exercise in Mild Cognitive Impairment (INHANCE-MCI)

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
84 (estimated)
Sponsor
Posit Science Corporation · Industry
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

This study is a validation study to evaluate efficacy of two neuroplasticity-based, computerized cognitive training programs to improve neurological and neuropsychological health in older adults with mild cognitive impairment (MCI).

Detailed description

The primary objective of this study is to evaluate will evaluate the impact of speed training to change cholinergic signaling, cognitive performance, and functional abilities in patients with MCI, as evidenced by \[18F\]fluoroethoxybenzovesamicol (FEOBV) positron-emission tomography (PET) and standard measures of cognition and function. The investigators will employ a prospective, double-blind, parallel-arm, active-controlled, randomized clinical trial in patients with clinically-defined mild cognitive impairment aged 65 and above with a baseline MoCA of 18-26 inclusive. Approximately 84 participants will be consented to ensure the successful completion of at least 70 participants (post 20% attrition). Participants will then complete the Screening (V0) assessments to determine eligibility. Following inclusion, participants will complete the Baseline (V1) assessments, PET imaging and structural MRI scan; participants will then be randomized into either the speed-based brain training or an active control of visual non-speeded computerized games and will engage in approximately 35 hours of program use for the 10-week Intervention Period. Following the 10-week intervention, participants will complete a Post-Intervention (V2) assessment, and PET imaging to evaluate changes in cognitive function. Participants will then stop using their assigned program for 3 months and return for a Follow-up (V3) end-of-study assessment and PET imaging to evaluate the endurance of changes in cognition, function, and behavior in the absence of further program use.

Conditions

Interventions

TypeNameDescription
OTHERComputerized speed-based cognitive trainingThirty minutes of training on computerized exercises that targets visual processing speed, memory, attention and alertness.
OTHERComputerized executive function cognitive trainingThirty minutes of training on computerized exercises that target executive function.

Timeline

Start date
2026-05-05
Primary completion
2027-05-31
Completion
2027-05-31
First posted
2025-11-24
Last updated
2026-03-06

Source: ClinicalTrials.gov record NCT07243600. Inclusion in this directory is not an endorsement.