Multiple Sclerosis Clinical Trial
Official title:
The Effects of an Innovative Combined Virtual Reality and Robot Assisted Gait Training on Cognitive and Walking Functions in Patients With Multiple Sclerosis: A Randomized Control Trial
Multiple Sclerosis (MS), the most common non-traumatic cause of neurologic disability in
young adults, affects mobility and ambulation in the majority of patients. Nearly 50% of
persons with MS will require an assistive device to ambulate within 10 years of diagnosis. A
subgroup of MS is Primary Progressive MS, which manifests with gait disturbances over 80% of
patients in the long term. In addition to altered gait, nearly 70% of patients will
experience cognitive deficits during the course of the disease. Therefore, actions that
facilitate patient involvement in finding solutions for personalized management of disease
and disability are needed.
Although immunomodulatory drugs offer some benefit in other types of Multiple Sclerosis,
there is currently no effective treatment for Primary Progressive MS. A fundamental goal in
the management of persons with MS is to maximize their ability to ambulate and perform safe
and effective transfers in everyday life.
In the last decade, research has increasingly centered on the effects of robot devices in
the rehabilitation of patients with neurological diseases. This has led to the development
of new robot-assisted gait devices engendered by virtual-reality systems, and several
studies have demonstrated the positive effects that these devices have on gait endurance and
quality of life in patients with neurological diseases and disability.
The aim of this project is to develop and study the effects of a novel, cognitively
intensive virtual-reality -based rehabilitation software application that simulates a
real-world environment where a person can walk. The virtual-reality application is an
upgrade version synchronized to a robotic device, the GEO System. The second aim is to
compare the cognitive and motor effects of robot-assisted gait training with this
application against training with robot-assisted gait training without virtual reality.
The experimental group will receive robot-assisted gait training with the virtual-reality
application and the control group will receive robot-assisted gait training All subjects
will undergo training for 6 weeks (2 sessions/week) for a total of 12 sessions. Assessments
before training, after training, and at follow-up will be performed using clinical and
instrumental tests to compare the effects of training.
Successful completion of the study may help patients to alleviate the impact of disability,
increase their independence in activities of daily life, and improve their quality of life.
Through new rehabilitative strategies that combine cognitive and motor training involving
higher brain functions and motivation, patients will be stimulated to walk in a
reality-based environment.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05528666 -
Risk Perception in Multiple Sclerosis
|
||
Completed |
NCT03608527 -
Adaptive Plasticity Following Rehabilitation in Multiple Sclerosis
|
N/A | |
Recruiting |
NCT05532943 -
Evaluate the Safety and Efficacy of Allogeneic Umbilical Cord Mesenchymal Stem Cells in Patients With Multiple Sclerosis
|
Phase 1/Phase 2 | |
Completed |
NCT02486640 -
Evaluation of Potential Predictors of Adherence by Investigating a Representative Cohort of Multiple Sclerosis (MS) Patients in Germany Treated With Betaferon
|
||
Completed |
NCT01324232 -
Safety and Efficacy of AVP-923 in the Treatment of Central Neuropathic Pain in Multiple Sclerosis
|
Phase 2 | |
Completed |
NCT04546698 -
5-HT7 Receptor Implication in Inflammatory Mechanisms in Multiple Sclerosis
|
||
Active, not recruiting |
NCT04380220 -
Coagulation/Complement Activation and Cerebral Hypoperfusion in Relapsing-remitting Multiple Sclerosis
|
||
Completed |
NCT02835677 -
Integrating Caregiver Support Into MS Care
|
N/A | |
Completed |
NCT03686826 -
Feasibility and Reliability of Multimodal Evoked Potentials
|
||
Recruiting |
NCT05964829 -
Impact of the Cionic Neural Sleeve on Mobility in Multiple Sclerosis
|
N/A | |
Withdrawn |
NCT06021561 -
Orofacial Pain in Multiple Sclerosis
|
||
Completed |
NCT03653585 -
Cortical Lesions in Patients With Multiple Sclerosis
|
||
Recruiting |
NCT04798651 -
Pathogenicity of B and CD4 T Cell Subsets in Multiple Sclerosis
|
N/A | |
Active, not recruiting |
NCT05054140 -
Study to Evaluate Efficacy, Safety, and Tolerability of IMU-838 in Patients With Progressive Multiple Sclerosis
|
Phase 2 | |
Completed |
NCT05447143 -
Effect of Home Exercise Program on Various Parameters in Patients With Multiple Sclerosis
|
N/A | |
Recruiting |
NCT06195644 -
Effect of Galvanic Vestibular Stimulation on Cortical Excitability and Hand Dexterity in Multiple Sclerosis Patients
|
Phase 1 | |
Completed |
NCT04147052 -
iSLEEPms: An Internet-Delivered Intervention for Sleep Disturbance in Multiple Sclerosis
|
N/A | |
Completed |
NCT03591809 -
Combined Exercise Training in Patients With Multiple Sclerosis
|
N/A | |
Completed |
NCT03594357 -
Cognitive Functions in Patients With Multiple Sclerosis
|
||
Completed |
NCT02845635 -
MS Mosaic: A Longitudinal Research Study on Multiple Sclerosis
|