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Recruiting NCT07034105

NCT07034105 Spatiotemporal Gait Parameters of Healthy and Stroke Patients During Overground, Treadmill, and Body Weight Supported Treadmill Walking

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Clinical Trial Summary
NCT ID NCT07034105
Status Recruiting
Phase —
Sponsor Bangladesh University of Engineering and Technology
Condition Gait Impairment in Stroke Patients
Study Type INTERVENTIONAL
Enrollment 25 participants
Start Date 2024-06-12
Primary Completion 2025-07-11

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
Gait Analysis

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 25 participants in total. It began in 2024-06-12 with a primary completion date of 2025-07-11.

⚠ 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

Gait impairments following a stroke significantly hinder mobility and quality of life, emphasizing the need for precise assessment methods to guide effective rehabilitation strategies. This study evaluates the variability and reliability of spatiotemporal gait parameters across three walking modalities: overground walking, treadmill walking, and body-weight-supported treadmill walking. Using a counterbalanced design, all participants undergo gait analysis in each modality to ensure unbiased and reliable comparisons. The study also incorporates a locally developed, cost-effective Body Weight Support System (BWSS) to address the limitations of accessibility in resource-constrained settings. By identifying how different modalities influence gait variability and reliability, this research aims to optimize rehabilitation outcomes and demonstrate the feasibility of implementing affordable gait analysis tools in clinical practice.

Eligibility Criteria

Inclusion Criteria: * Participants must be between 18 to 75 years old. * More than 1- month post stroke patient. * Participants must be able to walk with or without assistance. * Patients including both the male and female. * Participants must be able to provide informed consent to participate in the study. Exclusion Criteria: * Severe cognitive or communicative disorders. * Significant joint malposition. * Psychological, cognitive dysfunction, and any other neuromuscular problem. * Pregnant women will be excluded to avoid any potential risks to the mother and fetus. * Unstable cardiovascular disease like congenital heart disease, deep vein thrombosis, coronary heart disease, previous history of heart attack or heart failure.

Contact & Investigator

Central Contact

Muhammad Tarik Arafat, PhD

✉ tarikarafat@bme.buet.ac.bd

📞 01911764467

Principal Investigator

Muhammad Tarik Arafat, PhD

PRINCIPAL INVESTIGATOR

Department of Biomedical Engineering, Bangladesh University of Engineering and Technology (BUET), Dhaka - 1205.

Frequently Asked Questions

Who can join the NCT07034105 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Gait Impairment in Stroke Patients. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07034105 currently recruiting?

Yes, NCT07034105 is actively recruiting participants. Contact the research team at tarikarafat@bme.buet.ac.bd for enrollment information.

Where is the NCT07034105 trial being conducted?

This trial is being conducted at Dhaka, Bangladesh.

Who is sponsoring the NCT07034105 clinical trial?

NCT07034105 is sponsored by Bangladesh University of Engineering and Technology. The principal investigator is Muhammad Tarik Arafat, PhD at Department of Biomedical Engineering, Bangladesh University of Engineering and Technology (BUET), Dhaka - 1205.. The trial plans to enroll 25 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: November 2026  ·  Data Methodology