← Back to Clinical Trials
Recruiting NCT06191549

NCT06191549 Brain Stimulation Enhance Post-stroke Walking Survivors and Healthy Adults

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06191549
Status Recruiting
Phase —
Sponsor The University of Texas Medical Branch, Galveston
Condition Cerebral Vascular Accident
Study Type INTERVENTIONAL
Enrollment 70 participants
Start Date 2025-05-01
Primary Completion 2027-08-31

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 90 Years
Study Type INTERVENTIONAL
Interventions
anodal transcranial direct current stimulation (a-tDCS)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 70 participants in total. It began in 2025-05-01 with a primary completion date of 2027-08-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Recent studies showed that a non-invasive, low-intensity brain stimulation called transcranial direct current stimulation (tDCS) can effectively increase motor neuron excitability in the brain and therefore promotes functional recovery after stroke. Thus, the overall purpose of this research project is to examine the effect of brain stimulation on motor skill learning in stroke survivors.

Eligibility Criteria

Inclusion Criteria: * Age between 21 and 90 years * Medical history of a unilateral stroke occurring ≥ 6 months prior to enrollment * MRI or CT evidence from the imaging report shown that the stroke involves the corticospinal tract * Hemiparesis involving the lower extremity (Fugl-Meyer Lower Extremity Motor Test) * No passive range of motion limitation in bilateral hips and knees * Limitation of ankle passive range of motion to 10 degrees of dorsiflexion or less * Visual acuity can be corrected by glasses or contact lens to 20/20 * Able to walk independently with/without assistant devices for 10 meters * Able to maintain standing position without any assistance \>= 30 sec (Short Physical Performance Battery) * Evaluation of cognitive status: Mini-mental status examination (MMSE) score ≥ 24 Exclusion Criteria: * Pregnant women * MRI or CT evidence of involvement of the basal ganglia or cerebellum, evidence of multiple lesions, or evidence of any other brain damage or tumors * Have any metal implants, cardiac pacemakers, or history of seizures * Ongoing orthopedic or other neuromuscular disorders that will restrict exercise training * Any vestibular dysfunction or unstable angina * Significant cognitive deficits (inability to follow a 2-step command) or severe receptive or global aphasia

Contact & Investigator

Central Contact

Shih-Chiao Tseng, PhD

✉ shtseng@utmb.edu

📞 409-772-9555

Principal Investigator

Shih-Chiao Tseng, PhD

PRINCIPAL INVESTIGATOR

University of Texas

Frequently Asked Questions

Who can join the NCT06191549 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 90 Years, studying Cerebral Vascular Accident. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06191549 currently recruiting?

Yes, NCT06191549 is actively recruiting participants. Contact the research team at shtseng@utmb.edu for enrollment information.

Where is the NCT06191549 trial being conducted?

This trial is being conducted at Galveston, United States.

Who is sponsoring the NCT06191549 clinical trial?

NCT06191549 is sponsored by The University of Texas Medical Branch, Galveston. The principal investigator is Shih-Chiao Tseng, PhD at University of Texas. The trial plans to enroll 70 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology