Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
Healthy Volunteers
NCT05948930

Working Memory and Physical Exercise Training in Patients With Mild Cognitive Impairment

Led by University of Maryland, Baltimore · Updated on 2026-05-12

90

Participants Needed

1

Research Sites

186 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The prevalence of dementia will double in the next three decades in the U.S.; effective treatment or prevention for dementia is urgently needed. The current exploratory project aims to evaluate and understand how the brain and cognition may improve after a 12-week intervention that combines brain training and aerobic exercise training to improve brain function, both in those with mild cognitive impairment (some with possible prodromal Alzheimer's disease) and with healthy aging. Findings from this pilot project will guide and refine the development of a future larger clinical trial that aligns with the goals of the National Alzheimer's Plan of Action (NAPA), especially regarding "Prevent and Effectively Treat Alzheimer's Disease (AD) by 2025.

CONDITIONS

Official Title

Working Memory and Physical Exercise Training in Patients With Mild Cognitive Impairment

Who Can Participate

Age: 50Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 50 to 80 years of all races and ethnicities
  • Sedentary adults exercising less than three times per week for aerobic or combined training
  • Ability to use and access an iPad or computer for cognitive training or combined training
  • Fluent in English
  • Diagnosis of mild cognitive impairment confirmed by clinical dementia rating scale and Montreal Cognitive Assessment
  • Preserved independence in daily activities confirmed by caregiver interview and assessment
Not Eligible

You will not qualify if you...

  • No access to computer or internet for cognitive training and unwilling to come to the lab
  • Unable to undergo MRI due to claustrophobia or metal foreign bodies
  • Symptomatic heart disease, coronary artery disease, congestive heart failure, uncontrolled hypertension or diabetes, or other significant cardiovascular disorders preventing exercise
  • Neurologic, musculoskeletal, or other conditions limiting physical assessments
  • Estimated verbal IQ below 70 invalidating informed consent
  • Moderate to severe substance use disorder
  • Severe chronic or acute medical or neuropsychiatric conditions affecting cognition or brain imaging
  • Body mass index over 40 kg/m2

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Maryland Baltimore

Baltimore, Maryland, United States, 21201

Actively Recruiting

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Research Team

L

Linda Chang, M.D., M.S.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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