Multiple Sclerosis (MS) Clinical Trials

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Prospective, Placebo-controlled Study on the Functional and Quality of Life Effects of the Mollii Neuromodulatory Suit in Patients With Stroke and Multiple Sclerosis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

* Objective assessment of clinical symptoms resulting from stroke, as well as changes in mobility and quality of life, and determination of changes resulting from therapies * Objective assessment of the quality of life, functionality, and clinical symptoms of patients with multiple sclerosis (MS) and determination of changes resulting from therapies * Comparison of measured data from the two main neurological patient groups (stroke, multiple sclerosis) and follow-up of changes in relation to themselves and each other. * Mapping the role of the placebo effect in neuromodulation devices by comparing subjective and objective outcomes. * Analyzing the expectations and experiences of patients receiving placebo treatment using quality of life questionnaires. * Analyzing the effects of the Mollii suit among subgroups of MS and stroke patients. * Assessing the safety, possible side effects, and tolerability of the Mollii suit. * Mapping changes in gait pattern due to the effects of therapy using 3D motion analysis. * Examining the maintenance effects of neuromodulation during a 1-month follow-up.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

• suffered a first ischemic stroke, diagnosed by a neurologist based on CT or MR imaging

• neurological examination revealed mobility and postural limitations

• confirmed multiple sclerosis diagnosed by a neurologist based on MRI imaging

Locations
Other Locations
Hungary
Somogy County Kaposi Mór Teaching Hospital
RECRUITING
Kaposvár
Contact Information
Primary
Barbara Kopácsi
kbarbi0108@gmail.com
+36308340545
Backup
József Dr. habil. Tollár
tollarjozsef86@gmail.com
+36306994497
Time Frame
Start Date: 2026-01-12
Estimated Completion Date: 2028-08-01
Participants
Target number of participants: 40
Treatments
Experimental: Mollii Group
Receaving treatment with the stimulation program.
Placebo_comparator: Control Group
Receaving treatment without the stimulation program.
Related Therapeutic Areas
Sponsors
Leads: Somogy Megyei Kaposi Mór Teaching Hospital

This content was sourced from clinicaltrials.gov