Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
Healthy Volunteers
NCT04934956

Increasing Gait Automaticity in Older Adults by Exploiting Locomotor Adaptation

Led by University of Pittsburgh · Updated on 2025-08-03

42

Participants Needed

1

Research Sites

238 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The investigators will test the following: 1) the extent of locomotor adaptation improvement in individuals aged 65 years and older; 2) the association between initial walking automaticity (i.e. less PFC activity while walking with a cognitive load) and prefrontal-subcortical function (measured via neuropsychological testing); and 3) whether improvements in locomotor adaptability result in improvements in the Functional Gait Assessment (FGA), a clinically relevant indicator of dynamic balance and mobility in older adults. To answer these questions, the investigators will combine innovative techniques from multiple laboratories at the University of Pittsburgh. Automatic motor control (Dr. Rosso's expertise) will be assessed by wireless functional near-infrared spectroscopy (fNIRS) of the PFC during challenged walking conditions (walking on an uneven surface and walking while reciting every other letter of the alphabet). fNIRS allows for real-time assessment of cortical activity while a participant is upright and moving by way of light-based measurements of changes in oxygenated and deoxygenated hemoglobin. Locomotor adaptation (Dr. Torres-Oviedo's expertise) will be evaluated with a split-belt walking protocol (i.e., legs moving at different speeds) that the investigators and others have used to robustly quantify motor adaptation capacity in older individuals and have shown to be reliant on cerebellar and basal ganglia function. The investigators will focus on two important aspects of locomotor adaptation that the investigators have quantified before: (Aim 1) rate at which individuals adapt to the new (split) walking environment and (Aim 2) capacity to transition between distinct walking patterns (i.e., the split-belt and the overground walking patterns), defined as motor switching. Adaptation rate and motor switching are quantified using step length asymmetry, which is the difference between a step length taken with one leg vs. the other. The investigators will focus on this gait parameter because it robustly characterizes gait adaptation evoked by split-belt walking protocols. Finally, the investigators will quantify participant's cognitive function (Dr. Weinstein's expertise) through neuropsychological battery sensitive to prefrontal-subcortical function. The investigators will mainly focus on evaluating 1) learning capacity reliant on cerebellar structures and 2) assessing executive function heavily reliant on PFC and, to a lesser extent, the basal ganglia.

CONDITIONS

Official Title

Increasing Gait Automaticity in Older Adults by Exploiting Locomotor Adaptation

Who Can Participate

Age: 19Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 19 years old or older
  • Body Mass Index of 35 or less
  • Able to walk without a hand held device
  • Able to walk for 5 minutes at their self-paced speed
Not Eligible

You will not qualify if you...

  • History of neurological disorders, heart or respiratory disease, brain injury, seizures, spinal cord surgery, or strokes
  • Pregnancy
  • Unable to follow two part commands
  • Uncorrected vision or severe visual impairment with acuity less than 20/70
  • Cognitive impairments with modified mini-mental score less than 84
  • Orthopedic or pain conditions affecting lower extremities or back
  • Refusal to walk on a treadmill
  • Hospitalized within 6 months prior to the study for acute illness or surgery (except minor procedures)
  • Lower extremity orthopedic surgery within 1 year
  • Uncontrolled hypertension (greater than 190/110 mmHg)
  • Diagnosed dementia
  • Dyspnea at rest or during daily living activities
  • Use of supplemental oxygen, resting heart rate over 100 or under 40 beats per minute
  • Fixed or fused hip, knee, or ankle joints
  • Progressive movement disorder such as Multiple Sclerosis, Amyotrophic Lateral Sclerosis, or Parkinson's disease

AI-Screening

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Trial Site Locations

Total: 1 location

1

Sensorimotor Learning Laboratory, Schenley Place Suite 110

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

G

Gelsy Torres-Oviedo, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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