Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite
Not a traditional drug phase: Treadmill-integrated virtual reality gait training for Multiple Sclerosis
This study will test whether a treadmill-based virtual reality walking program is safe, practical, and helpful for people with multiple sclerosis (MS). Participants will complete a 6-week training program and wear smart socks that measure how they walk before, during, and after the program.
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are Treadmill-integrated virtual reality gait training. The registry lists allocation as na. This study will test whether a treadmill-based virtual reality walking program is safe, practical, and helpful for people with multiple sclerosis (MS).
They plan to enroll about 10 people at Atlanta. Taking part typically means study visits and measurements plus check-ins.
Official title (unrewritten)
Investigating the Acute and Long-term Effects of Treadmill-integrated Virtual Reality (VR) Training on Real-World Mobility and Fall-Related Outcomes in People With Multiple Sclerosis
Interventions: Treadmill-integrated virtual reality gait training
Primary outcome (registry wording): Spatiotemporal metrics of gait
Who it is for (from inclusion criteria)
Ages 18 Years to any
Have a clinically confirmed diagnosis of multiple sclerosis (MS)
Be 18 years of age or older
Demonstrate ≥10% variability in stride length, step length, or gait asymmetry
Can ambulate without an assistive device, with a unilateral, or with a bilateral assistive device
Demonstrate no more than mild cognitive impairment, indicated by the Mini-Mental State Exam (score \>19)
Possess adequate cognitive function to understand and follow research instructions
Be able to safely participate in the study and training procedures as determined by study staff
Who the registry excludes
Have a diagnosis of any other neurological condition or recent orthopedic conditions that affects gait, balance, or mobility
Exhibit \<10% variability in stride length, step length, or gait asymmetry
Are unable to ambulate (i.e. wheelchair bound or bedbound individuals)
Have legal blindness or severe visual impairment that would interfere with virtual reality engagement or safe ambulation
Have a body weight exceeding 300 lbs., which exceeds the safety limits of the treadmill and body weight support system
Have uncontrolled or untreated hypertension, hypotension, or angina
Have a past or current history of epilepsy or any other type of seizure disorder, whether controlled or uncontrolled
We will investigate the clinical manifestations and molecular genetic defects of heritable urologic malignant disorders. Families with urologic malignancy with known or suspected genetic basis will be enrolled.
This protocol will evaluate patients with systemic lupus erythematosus (SLE) and their relatives to learn more about how the disease develops and changes over time. It will also study genetic factors that make a person susceptible to SLE.
This study is designed to explore the genetics and pathophysiology of diseases presenting with intermittent fever, including familial Mediterranean fever, TRAPS, hyper-IgD syndrome, and related diseases. The following individuals may be eligible for this natural history study: 1) patients with known or suspected familial Mediterranean fever, TRAPS, hyper-IgD syndrome or related disorders; 2) relatives of these patients; 3) healthy, normal volunteers 7 years of age or older.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT07927439?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT07927439?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.