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Enrolling by invitation NCT07474038

AI-Supported Cognitive Rehabilitation for Older Adults With Mild Cognitive Impairment

No phase Interventional Mild Cognitive Impairment (MCI)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: AI-Supported Cognitive Rehabilitation.
Who it may be relevant to
Registry conditions: Mild Cognitive Impairment (MCI). Basic parameters: from 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluating the Efficacy of AI-Augmented Cognitive Rehabilitation in Mild Cognitive Impairment

Overview

Mild cognitive impairment (MCI) is associated with increased risk of progression to dementia, highlighting the need for accessible interventions to support cognitive health. This randomized controlled trial will evaluate the safety and efficacy of a 12-month artificial intelligence (AI)-supported cognitive rehabilitation program for older adults with MCI. Participants will be recruited from an existing research study conducted within Kaiser Permanente Southern California and randomized 1:1 to either (1) AI-supported cognitive rehabilitation or (2) usual care alone. The intervention combines clinician-delivered telehealth cognitive rehabilitation sessions with daily AI-guided cognitive exercises and education. The primary outcome is change in global cognition at 6 months measured by the Montreal Cognitive Assessment (MoCA)-BLIND. Secondary outcomes at 6 and 12 months include additional measures of cognition, subjective memory, goal attainment, mood, and loneliness. Exploratory outcomes include engagement with the AI intervention and health-related behavioral outcomes derived from electronic health record data. Participant safety will be monitored throughout the study through adverse event tracking, review of AI interactions for safety concerns, and predefined procedures for responding to psychological or clinical risk. This study will determine whether integrating AI-guided cognitive exercises with clinician-delivered rehabilitation improves cognitive and related outcomes in older adults with MCI compared to usual care.

Detailed description

Background and Rationale:

Mild cognitive impairment (MCI) represents a transitional stage between normal aging and dementia and is associated with elevated risk of progression to Alzheimer's disease and related dementias. Individuals with MCI frequently report functional challenges, reduced confidence, and increased risk of mood symptoms. Although cognitive rehabilitation and cognitive stimulation interventions have demonstrated benefit, traditional models are resource-intensive and limited in frequency, personalization, and scalability.

Advances in artificial intelligence (AI) allow delivery of adaptive, conversational, and personalized cognitive exercises at high frequency. However, AI-only approaches may lack the contextualization, goal-setting support, and therapeutic oversight provided by trained clinicians. A blended care model integrating AI-guided cognitive exercises with clinician-delivered telehealth rehabilitation may provide both scalability and clinical depth. This study evaluates the safety, engagement, and clinical efficacy of such an integrated model.

Study Design:

This is a prospective, randomized parallel controlled trial conducted within Kaiser Permanente Southern California. Participants diagnosed with MCI through an existing cognitive assessment research program will be randomized in a 1:1 ratio to:

* AI-supported cognitive rehabilitation * Usual care alone

The intervention period is 12 months, with primary outcome assessment at 6 months and follow-up through 12 months.

Intervention:

Participants randomized to the intervention will receive a structured cognitive rehabilitation program consisting of two integrated components:

1. Clinician-Delivered Telehealth Rehabilitation Licensed clinical social workers trained in cognitive rehabilitation will deliver goal-directed sessions via telehealth every two weeks for the first six months and monthly for the remaining six months. Sessions are delivered within a reablement framework and may incorporate cognitive rehabilitation techniques, behavioral activation, compensatory strategy training, and elements of cognitive behavioral and mindfulness-based approaches, tailored to individual patient needs. 2. AI-Guided Cognitive Sessions Participants will engage in daily AI-powered conversational sessions (approximately 10-30 minutes per session). These sessions provide structured cognitive stimulation, cognitive training exercises, and psychoeducation. Content delivery is guided by algorithms that adapt based on participant interaction patterns and clinician input. The AI system is not intended for diagnostic or autonomous clinical decision-making.

Participants randomized to usual care will continue to receive standard health plan services and complete study assessments at scheduled time points. They will be offered the cognitive rehabilitation program at the end of the study if the intervention is determined to be safe and efficacious.

Safety Oversight and Risk Monitoring:

Given the use of AI-based conversational technology in a cognitively vulnerable population, safety monitoring procedures are integrated at multiple levels:

* Licensed clinicians monitor participant progress and well-being throughout the intervention period. * AI interactions are reviewed for safety concerns, including indicators of psychological distress. * Predefined escalation procedures are in place for emergent behavioral health risk, including referral to appropriate clinical services and crisis resources. * Technical concerns or adverse events are tracked and reviewed by the study team. * The principal investigator oversees participant safety and protocol adherence in accordance with IRB and Good Clinical Practice standards.

Interventions

  • Behavioral AI-Supported Cognitive Rehabilitation
    Participants receive a structured cognitive rehabilitation program consisting of (1) telehealth sessions delivered by licensed clinicians using a goal-directed cognitive rehabilitation framework and (2) daily AI-guided conversational cognitive exercises tailored to individual needs. The AI system provides cognitive stimulation, training exercises, and psychoeducation but does not perform diagnostic or autonomous clinical decision-making.

Primary outcome measures

  • Change in MoCA-BLIND Score at 6 Months [Time frame: 6 months]
Secondary outcome measures (6)
  • Change in Global Cognition (MoCA-BLIND) [Time frame: 12 months]
  • Change in Global Cognition (ACE-III) [Time frame: 6 months and 12 months]
  • Change in Subjective Memory [Time frame: 6 months and 12 months]
  • Change in Mood Symptoms [Time frame: 6 months and 12 months]
  • Change in Loneliness [Time frame: 6 months and 12 months]
  • Change in Goal Attainment [Time frame: 6 months and 12 months]

Eligibility criteria

Inclusion criteria

  • Age 65 years or older
  • Diagnosis of mild cognitive impairment (MCI)
  • Montreal Cognitive Assessment (MoCA)-BLIND adjusted score (13-18)
  • Able to provide informed consent
  • English fluency sufficient to complete study assessments and participate in intervention sessions
  • Access to and ability to use a computer or mobile device with internet connectivity

Exclusion criteria

  • Current receipt of ongoing behavioral health treatment or psychotherapy from a Kaiser Permanente clinician
  • Diagnosis of bipolar disorder, schizophrenia spectrum disorder, or other serious mental illness that would interfere with participation
  • Significant communication impairment that would prevent participation in conversational or telehealth sessions

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Kaiser Permanente Southern California — Pasadena

Identifiers

NCT: NCT07474038 · 14432

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗