Telehealth Cognitive Training for Mild Cognitive Impairment

This study is testing two versions of a telehealth (virtual) cognitive training program for people aged 65-84 with Mild Cognitive Impairment (MCI), a condition that can affect memory and thinking. One program, called ME-CCT-MCI, lasts eight weeks, and the other, bME-CCT-MCI, is a shorter five-week version. Researchers want to see if the shorter five-week program is just as good as the eight-week program at improving your thinking abilities, quality of life, and how you feel about your memory. You'll need to be able to speak English and have a study partner (like a family member) available for some parts of the study. The study aims to enroll 100 participants, but its current status is unclear.

Study design
This interventional study plans to enroll 100 participants to compare two different lengths of cognitive training programs.
What's involved
You will complete a screening visit with a study partner, followed by virtual cognitive training sessions and tests of memory and thinking.
Compensation
Not stated in the trial record.
Follow-up
Your cognition, quality of life, and subjective cognition will be measured at the end of treatment and three months after treatment ends.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07366346

Telehealth-Adapted Compensatory Training and Intervention for Cognition

Recruiting
NAAges 65–84InterventionalTreatment
University of Florida
~100 participants
Updated 2026-06-03 on ClinicalTrials.gov
What's tested:Motivationally Enhanced Compensatory Cognitive Training for Mild Cognitive Impairment (ME-CCT-MCI)Brief Motivationally Enhanced Compensatory Cognitive Training for Mild Cognitive Impairment (bME-CCT-MCI)

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in cognition
Measured over Baseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)
+7 more outcomes measured
MCI
Mild Cognitive Impairment
Mild Cognitive Impairment (MCI)

NCT07366346

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of Florida

    Gainesville, Floridano site contact published

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Cameron K Perrin, M.S. · PRINCIPAL_INVESTIGATOR · University of Florida
  • Joseph M Gullett, Ph.D. · PRINCIPAL_INVESTIGATOR · University of Florida

Opens a ready-to-send draft in your own email app — review before sending.

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

65 years of age or older, less than 85 years
Have the ability to speak and understand English
Time and willingness to commit to the completion of this study
Availability of a study partner (typically a relative, spouse, offspring, or roommate) for initial and post-intervention testing
A global Clinical Dementia Rating scale (CDR) score of 0.5 and cognitive performance of \<26 on the Montreal Cognitive Assessment (MoCA) or \<19 on the MoCA-BLIND for categorization of MCI, as determined in the screening appointment.

Exclusion

Self-reported diagnosis of dementia or functional impairment that requires assistance
Recent changes in medications for memory (i.e., prescribed or changed medications for memory within 30 days)
Major psychiatric illness (schizophrenia, current substance dependence, or undertreated depression or anxiety), or 15-item Geriatric Depression Scale (GDS-15) score of eight or higher
Hearing, vision, or motor deficits that would interfere with standardized cognitive assessment or participation in study interventions: e.g., inability to hear through headphones (with or without hearing aids). If vision is corrected with lenses to appropriate levels, then participant will be eligible
No access to reliable, stable internet, OR
Current participation in another cognitive training program or treatment study.
  • Change in cognitionBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the National Alzheimer's Coordinating Center Uniform Data Set version 4 (NACC-UDSv4). This full neuropsychological assessment consists of neuropsychological tests including: Montreal Cognitive Assessment (MoCA)-BLIND, Craft Story 21, Benson Complex Figure, Number Span Test (Forward and Backward), Category Fluency, Trail Making Test, Verbal Fluency: Phonemic Test, Rey Auditory Verbal Learning Test (RAVLT), and Multilingual Naming Test (MINT). On most of these tasks a higher score indicates better cognition, except for on Trail Making Test, where a lower score indicates faster time (better cognition).

  • Change in quality of lifeBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the Quality of Life in Alzheimer's Disease (QOL-AD), completed by participant and study partner, where higher scores indicate better quality of life (range 13-52).

  • Change in subjective cognitionBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form v2.0 Cognitive Function 8a, a self-report cognitive functioning questionnaire, where a higher score indicates better reported cognition (range 8-40).

  • Change in reported daily functioningBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the National Alzheimer's Coordinating Center (NACC) Functional Assessment Scale (FAS), completed by the study partner, where a lower score indicates more independence (range 0 to 30).

  • Change in objective functional statusBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the internet-based Bill-Paying Task, an objective measure of functional status which can be administered online, as a test of participants' ability to pay fictional bills. A higher score indicates more severe deficits (range 0-25).

  • Change in anxietyBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the Generalized Anxiety Disorder 7-item (GAD-7) scale, a self-report questionnaire of anxiety, where higher scores indicate higher levels of anxiety (range 0 to 21).

  • Change in depressionBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the Geriatric Depression Scale (GDS), a self-report questionnaire of depression, where higher scores indicate higher levels of depression (range 0 to 15).

  • Change in caregiver burdenBaseline, end of treatment (5 or 8 weeks after baseline, up to 7 or 10 weeks after baseline), and three months after end of treatment (18 or 21 weeks after baseline, up to 20 or 23 weeks after baseline)

    As assessed by the Zarit Burden Interview (ZBI), completed by study partner, where a higher score indicates higher burden (range 0 to 48).