Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT05830942

Up-2 Study: Cognitively Engaging Walking Exercise and Neuromodulation to Enhance Brain Function in Older Adults

Led by University of Florida · Updated on 2025-05-08

120

Participants Needed

2

Research Sites

158 weeks

Total Duration

On this page

Sponsors

U

University of Florida

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Declines in cognitive function and walking function are highly intertwined in older adults. A therapeutic approach that combines complex (cognitively engaging) aerobic walking exercise with non-invasive electrical brain stimulation may be effective at restoring lost function. This study tests whether electrical stimulation of prefrontal brain regions is more beneficial than sham stimulation.

CONDITIONS

Official Title

Up-2 Study: Cognitively Engaging Walking Exercise and Neuromodulation to Enhance Brain Function in Older Adults

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 or older
  • Mild to moderate decline in executive function based on standardized tests
  • Experience of worsening confusion or memory loss in the past 12 months
  • Ability to walk independently for 6 minutes, with or without a cane
Not Eligible

You will not qualify if you...

  • Major cognitive disorder that affects independence
  • Scoring below the 10th percentile on cognitive assessments
  • Taking medications that may influence brain stimulation effects
  • Contraindications to transcranial direct current stimulation or MRI

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

University of Florida

Gainesville, Florida, United States, 32610

Actively Recruiting

2

Brooks Rehabilitation

Jacksonville, Florida, United States, 32653

Actively Recruiting

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Research Team

D

David J Clark, ScD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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