NCT07492602Not yet recruiting
Comparison of Gait Metrics in Patients With Stroke, Traumatic Brain Injury, and Multiple Sclerosis
Comparison of Gait Metrics in Patients With Stroke, Traumatic Brain Injury, and Multiple Sclerosis Before and After Functional Electrical Stimulation
Source: ClinicalTrials.gov · Last updated 27 Mar 2026
Brief summary (registry, in English)
People with neurological conditions often have difficulty walking, including problems such as foot drop. Functional electrical stimulation (FES) is a treatment that uses electrical signals to activate muscles and support walking. The L300 device is designed to help lift the foot during each step. This study will evaluate how using the L300 affects walking performance. Researchers will measure walking speed, step length, and walking symmetry using objective gait assessment tools. The study will also explore whether people with different neurological conditions respond differently to FES. The goal of this research is to improve understanding of how FES influences walking and to support more personalized rehabilitation approaches.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- First submitted
- 17 Mar 2026
- Start date
- 1 Apr 2026
- Primary completion date
- 1 Feb 2027
- Lead sponsor
- Casa Colina Hospital and Centers for Healthcare
- Diseases
- Stroke, Multiple sclerosis
- NCT number
- NCT07492602
What you commit to
- Study type: Interventional
- Planned participants: 90
- From 1 Apr 2026 to the primary completion date, 1 Feb 2027
- 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
- Severe lower limb contractures or orthopedic conditions that limit gait.
- Uncontrolled medical conditions (e.g., severe cardiac disease).
Other
- Implanted electrical devices (e.g., pacemaker) contraindicating FES use.
- Pregnancy.
- Skin integrity issues preventing electrode placement.
- Participation in other interventional gait studies within the past 3 months.
Who the study is looking for
- Adults aged 18-80 years.
- Diagnosis of stroke, traumatic brain injury, or multiple sclerosis confirmed by medical records.
- Presence of foot drop or impaired ankle dorsiflexion during gait.
- Ability to ambulate at least 10 meters with or without assistive devices.
- Cognitive ability to follow simple instructions and provide informed consent.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept 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 |
|---|---|---|---|
| Casa Colina Hospital and Centers for Healthcare Coordinator of this site? Confirm its status | Pomona | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.