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Cognition and Motor Learning Post-stroke

Cognition as a Moderator of Motor Learning Post-stroke

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04829071
Enrollment
65
Registered
2021-04-02
Start date
2023-01-16
Completion date
2026-12-14
Last updated
2025-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CVA (Cerebrovascular Accident), Stroke

Keywords

stroke, walking, rehabilitation, cognition

Brief summary

This project seeks to determine how post-stroke cognitive impairment moderates motor learning during walking in older adults with chronic stroke and identify brain structural markers that mediate this relationship. The chosen experimental design integrates biomechanical analyses, neuropsychological assessments, and brain imaging techniques to determine the impact of post-stroke cognitive impairment severity on two forms of motor learning (explicit and implicit) and examine the role of the dorsolateral prefrontal cortex in the relationship between cognition and explicit motor learning. Ultimately, this work may lead to the development of a more comprehensive, effective treatment approach to improve walking dysfunction in older adults post-stroke.

Interventions

BEHAVIORALExplicit motor learning

Participants will be provided with visual feedback of their right and left step lengths on a screen in front of a treadmill.

BEHAVIORALImplicit motor learning

Participants will walk on a treadmill that drives their right and left legs to move at two different speeds.

Sponsors

University of Southern California
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Unilateral stroke * Stroke occurred more than 6 months prior * Paresis confined to one side * Independently ambulatory (including the use of assistive devices) * Able to walk for 5 minutes without stopping * Answers no to all general health questions on the PAR-Q+ * Willingness to complete study procedures

Exclusion criteria

* Brainstem or cerebellar stroke * Aphasia (expressive, receptive, or global) * Any major musculoskeletal or non-stroke neurological condition that interferes with the assessment of sensorimotor or cognitive function * Metal in the head (except in the mouth), implanted cranial or thoracic devices that violate MRI safety regulations * Uncontrolled hypertension (\>160/110mmHg) * Concurrent physical therapy * Claustrophobia * Significant cognitive deficit or dementia (\<20 on MoCA) * Inability to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
step length asymmetry - change in performanceMeasured at three timepoints of interest within each testing session: baseline and at the beginning and end of the interventions; participants will complete 2 testing sessions over approximately 1 monthscharacterized as a comparison between the right and left step lengths; captured to quantify change in performance with biofeedback or split belt walking

Secondary

MeasureTime frameDescription
step length asymmetry - immediate retentionMeasured after motor learning in each testing session; participants will complete 2 testing sessions over approximately 1 monthscharacterized as a comparison between the right and left step lengths; captured to quantify the retention of a newly learned walking pattern

Countries

United States

Contacts

Primary ContactKristan Leech, PT, DPT, PhD
kleech@pt.usc.edu(323) 442-1583
Backup ContactSarah Kettlety, MS
kettlety@usc.edu(323) 442-1196

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026