NCT06374706Completed
Effects of Rehabilitation Robots-Morning Walk in Individuals With Hemiparesis
Effects of End-Effector Type Rehabilitation Robots-Morning Walk on Symmetrical Walking Patterns in Individuals With Hemiparesis
Source: ClinicalTrials.gov · Last updated 10 Apr 2025
Brief summary (registry, in English)
In this study, our objective is to explore and evaluate interventions to improve the process of recovery following a stroke. The main focus is on enhancing symmetrical walking patterns in adults who have experienced neurological deficits due to a stroke. The primary tool will be an end-effector type rehabilitation robot, the Morning Walk®. This robot has been specifically designed to assist in enhancing symmetrical walking patterns for individuals recovering from a stroke Morning Walk® has received approval from the FDA, meaning it meets stringent safety and efficacy standards.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 37 (actual)
- First submitted
- 24 Mar 2024
- Start date
- 30 May 2024
- Primary completion date
- 18 Feb 2025
- Lead sponsor
- The University of Texas Medical Branch, Galveston
- Diseases
- Stroke
- NCT number
- NCT06374706
What you commit to
- Study type: Interventional
- Participants enrolled: 37
- From 30 May 2024 to the primary completion date, 18 Feb 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Stroke secondary to subarachnoid hemorrhage or posterior circulation stroke.
- Poorly controlled diabetes, exemplified by conditions such as foot ulceration.
- Progressive neurological diseases.
- Congestive cardiac failure.
- Unstable angina.
- Peripheral vascular disease.
- Neuropsychiatric disorders, including dementia, cognitive deficits, and severe depression.
Other
- Life expectancy of less than one year.
- Comatose state.
- Inability to follow 3-step commands.
- Amputation.
- Blindness.
- Comprehensive aphasia.
- Medical instability.
- Significant musculoskeletal problems.
Who the study is looking for
- For this study, twenty volunteers fulfilling the inclusion criteria from participating physical therapy facilities and the local community will be recruited. The criteria for participants with a history of stroke include: Age 20 or older.
- Experienced a unilateral first stroke, either ischemic or hemorrhagic, in the carotid artery distribution.
- Diagnosed with stroke at least one month prior to participating in the study.
- Free from major post-stroke complications, such as recurrent stroke, hip fracture, or myocardial infarction.
- Residing within the community.
- Capable of ambulating 10 meters with or without the use of assistive devices.
Age in the registry: 20 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Texas Medical Branch Coordinator of this site? Confirm its status | Galveston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.