NCT07529054Recruiting
The Potential of Robotic-Assisted Gait Training in a Rehabilitation Setting
The Potential of Robotic-Assisted Gait Training in a Rehabilitation Settin
Source: ClinicalTrials.gov · Last updated 14 Apr 2026
Brief summary (registry, in English)
Robotic-assisted gait training (RAGT) devices, such as the Lokomat®, are commonly used to support gait rehabilitation by enabling repetitive, task-specific walking movements. The functional proprioceptive stimulation (FPS) device Vibramoov® represents a novel technology designed to stimulate proprioceptors at the muscle-tendon junction through targeted vibratory stimuli, thereby activating sensorimotor centers in the brain and potentially facilitating movement execution. The aim of this randomized controlled trial is to investigate whether Lokomat® training combined with Vibramoov® leads to greater improvements in qualitative and quantitative gait parameters in stroke patients compared with Lokomat® training alone. The study will be conducted at the Gröbming Rehabilitation Center and will include patients undergoing a four-week neurological inpatient rehabilitation program. Participants will be randomly assigned to an intervention group (Lokomat® + Vibramoov®) or a control group (Lokomat® only), with 20 patients per group. Primary outcomes include the 6-Minute Walk Test (6MWT) and spatiotemporal gait parameters. Additional assessments include functional scores, patient-reported outcome measures, and blood biomarkers. Statistical analyses will be performed depending on data distribution. A follow-up assessment evaluating EQ-5D and PHQ-4 will be conducted six months after completion of the rehabilitation program.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- First submitted
- 7 Apr 2026
- Start date
- Jan 2026
- Primary completion date
- Feb 2027
- Lead sponsor
- Ludwig Boltzmann Institute for Arthritis and Rehabilitation
- Diseases
- Stroke
- NCT number
- NCT07529054
What you commit to
- Study type: Interventional
- Planned participants: 40
- From Jan 2026 to the primary completion date, 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
- The presence of any comorbidity or disability other than stroke that would preclude gait training
- Any uncontrolled health condition for which exercise is contraindicated
Who the study is looking for
- Diagnosis of stroke (ischemic or hemorrhagic) ≥ 3 months
- Age ≥ 18a and ≤ 80a
- 6MWT ≤ 200m
- Barthel Index ≤ 95
- Mini Mental State Exam (MMSE) ≥ 24
- FAC: ≤ 4
- BBS): ≤49
- Modified Ashworth Scale (MAS): 0-3 for the lower extremity
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 |
|---|---|---|---|
| Reha-Zentrum Gröbming Coordinator of this site? Confirm its status | Gröbming | Austria | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.