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Recruiting NCT06268041

NCT06268041 HIT-Stroke Trial 2

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Clinical Trial Summary
NCT ID NCT06268041
Status Recruiting
Phase
Sponsor University of Cincinnati
Condition Stroke
Study Type INTERVENTIONAL
Enrollment 156 participants
Start Date 2024-02-09
Primary Completion 2028-01

Eligibility & Interventions

Sex All sexes
Min Age 30 Years
Max Age 85 Years
Study Type INTERVENTIONAL
Interventions
Moderate-Intensity Aerobic TrainingHigh-Intensity Interval Training

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 156 participants in total. It began in 2024-02-09 with a primary completion date of 2028-01.

⚠ 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

People who had a stroke at least 6 months prior and who still have difficulty with walking will each be randomly assigned to receive either moderate or vigorous intensity walking exercise. Both protocols will be performed individually with a physical therapist for 45 minutes, 3x/week for 12 weeks. Measures including walking function will be assessed at baseline (PRE), after 4, 8 and 12 weeks of training (12WK) and at 3-month follow up (3moPOST), by raters who are unaware of the participant randomization.

Eligibility Criteria

Inclusion Criteria: * Age 30-85 years at time of consenting * Hemiparesis from ischemic and/or hemorrhagic strokes * Most recent stroke for which participant sought treatment, at least 6 months prior to study consent * Walking speed \<1.0 m/s on the 10-meter walk test * Able to walk 10m over ground with assistive devices as needed and no continuous physical assistance from another person (guarding and intermittent assistance for loss of balance allowed) * Able to walk at least 3 minutes on the treadmill at ≥0.13m/s (0.3 mph) * Stable cardiovascular condition (AHA class B, allowing for aerobic capacity \<6 metabolic equivalents) * Able to communicate with investigators, follow a 2-step command and correctly answer consent comprehension questions Exclusion Criteria: * Exercise testing uninterpretable for ischemia or arrhythmia (e.g. resting ECG abnormality that makes exercise ECG uninterpretable for ischemia and no other clinical testing from the past year available to rule out these conditions) * Evidence of significant arrhythmia or myocardial ischemia on treadmill ECG graded exercise test in the absence of recent (past year) more definitive clinical testing (e.g. stress nuclear imaging) with negative result * Hospitalization for cardiac or pulmonary disease within past 3 months * Implanted pacemaker or defibrillator with an upper heart rate limit that would interfere with exercise testing or prescription, or with unknown limit * Significant ataxia or neglect (score of 2 on NIH stroke scale item 7 or 11) * Severe lower limb spasticity (Ashworth \>2) * Known recent history (\<3 months) of unstable substance abuse or unstable mental illness * Major post-stroke depression (Patient Health Questionnaire \[PHQ-9\] ≥ 10) in the absence of depression management by a health care provider * Currently participating in physical therapy or another interventional study targeting walking function * Recent (\<2 weeks) or planned changes in lower limb orthotic or spasticity management * Foot drop or lower limb joint instability without adequate stabilizing device, as assessed by a physical therapist * Clinically significant neurologic disorder other than stroke or unable to walk outside the home prior to stroke * Unable to walk outside the home prior to stroke * Other significant medical condition likely to limit improvement or jeopardize safety as assessed by a physical therapist (e.g. joint contracture, gait limited by pain) * Pregnancy * Previous exposure to fast treadmill walking (\>3 cumulative hours) in the past year

Contact & Investigator

Central Contact

Audrey Nicoloff

✉ strokerecovery@uc.edu

📞 513-558-7487

Principal Investigator

Pierce Boyne, PT, DPT, PhD

PRINCIPAL INVESTIGATOR

University of Cincinnati

Frequently Asked Questions

Who can join the NCT06268041 clinical trial?

This trial is open to participants of all sexes, aged 30 Years or older, up to 85 Years, studying Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06268041 currently recruiting?

Yes, NCT06268041 is actively recruiting participants. Contact the research team at strokerecovery@uc.edu for enrollment information.

Where is the NCT06268041 trial being conducted?

This trial is being conducted at Newark, United States, Kansas City, United States, Cincinnati, United States.

Who is sponsoring the NCT06268041 clinical trial?

NCT06268041 is sponsored by University of Cincinnati. The principal investigator is Pierce Boyne, PT, DPT, PhD at University of Cincinnati. The trial plans to enroll 156 participants.

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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: September 2026  ·  Data Methodology