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AI Prediction of Cognitive Training Response in Amnestic Mild Cognitive Impairment

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Study Aim

This study aims to evaluate how well artificial intelligence can predict the response to cognitive training in individuals with amnestic mild cognitive impairment, focusing on changes in visual attention abilities.

What is being tested

Cognitive Training

+ Computerized Cognitive Stimulation

Behavioral
Who is being recruted

From 55 to 100 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: October 2023
See protocol details

Summary

Principal SponsorUniversity of Florida
Study ContactJoseph Gullett, Ph.D.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 9, 2023

Actual date on which the first participant was enrolled.

This study is focused on enhancing brain function in older adults experiencing a specific type of memory problem known as amnestic mild cognitive impairment (aMCI). It aims to test the effectiveness of a cognitive training program delivered through an iPad application called the Posit Science Brain HQ Suite. This program is designed to help improve memory and thinking skills by engaging users in adaptive exercises for 60 minutes, two to three times a week, over a 16-week period. The research is important because it seeks to find new ways to slow down or improve memory problems that affect many older adults, potentially offering a simple and accessible way to enhance cognitive health. Participants in the study are divided into different groups, some receiving cognitive training while others receive a different type of activity as a control. The study measures improvement by looking at changes in specific cognitive skills before and after the training using tests like the Useful Field of View (UFOV) task. Additionally, detailed brain scans are performed at the beginning of the study to help predict who will benefit most from the training. The results are analyzed using advanced computer methods to identify patterns that might indicate success in cognitive improvement. This information could lead to better, personalized treatment options for individuals with aMCI in the future.

Official TitleUsing Artificial Intelligence to Predict Cognitive Training Response in Amnestic Mild Cognitive Impairment
NCT05903573
Principal SponsorUniversity of Florida
Study ContactJoseph Gullett, Ph.D.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

75 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 55 to 100 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: * Evidence of changed cognition reported by a close informant as obtained by an interview with a licensed clinical psychologist (PI, Gullett) * Cognitive performance on one or more standardized neuropsychological measures of verbal or non-verbal memory \> 1.0 standard deviation or more below the normative mean for age and education * No evidence of reported dependence in instrumental functional abilities (IADLs) despite reported cognitive difficulties * No evidence of dementia based on cognitive screening (Montreal Cognitive Assessment Score within normal limits for age, education, and sex using the NACC Uniform Data Set (UDS) norms. * Global clinical dementia rating scale (CDR) score must be equal to 0.5 * Willingness to be randomized into either the educational training (control) or intervention (cognitive training) group * Able and willing to devote 12 weeks to the intervention with additional time for pre- and post-testing * Able and willing to perform cognitive and emotional measures both on paper and on a tablet computer * In line with the recommendations of the SCD task force, an informant must be available. This is to a) obtain information about the participant's complaints and cognitive difficulties on interview, and b) to ascertain validity of self-reported IADL function in regard to instrumental functional activities. Exclusion Criteria: * Sensory loss (vision, hearing) or motor deficits that would preclude participation in the experimental tasks or neuropsychological assessment * English as a second language * Inability to undergo brain imaging due to claustrophobia or implants such as pacemakers, heart valves, brain aneurysm clips, orthodontics, non-removable body jewelry, or shrapnel containing ferromagnetic metal * Previous major strokes or other known significant brain abnormalities or diseases affecting the brain and/or cognition (e.g., Parkinson disease, multiple sclerosis, seizure disorder, brain surgery, moderate TBI, REM Behavior Sleep Disorder, untreated sleep apnea, etc.) * Unstable and uncontrolled medical conditions (metastatic cancer, HIV, moderate-severe kidney disease, uncontrolled diabetes, uncontrolled hypertension, severe cardiac disease, etc.). No current cancer diagnosis * Current or past history of major psychiatric disturbance including schizophrenia, or active psychosis, bipolar disorder, current major depressive episode, current alcohol or substance abuse or history thereof within the past six months. The investigators are not excluding individuals who are taking antidepressant or anti-anxiety medications, however, use of these medications will be recorded and data analyzed in post-hoc analyses * Use of antipsychotics, sedatives, or other medications with significant anticholinergic properties (due to potential influence on memory) * Use of photo-sensitive medications such as steroids or retin-A within 15 days of the study intervention. * Previous participation in a cognitive training study within the last 6 months or current involvement in another study involving cognitive, physical or other intervention at the time of participation.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants will complete computerized cognitive training via Posit Science Brain HQ. The duration is 60 min/day; the frequency is two to three days/wk, for 16 weeks with the goal of completing 40 sessions.

Group II

Active Comparator
Participants will complete cognitively-stimulating computer activities. The duration is 60 min/day; the frequency is two to three days/wk, for 16 weeks with the goal of completing 40 sessions.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

University of Florida

Gainesville, United StatesOpen University of Florida in Google Maps
Recruiting
One Study Center