Actively Recruiting
The EXOPULSE Study - a Database for Routine Follow-up of Clinical Outcomes
Led by Exoneural Network AB · Updated on 2026-02-27
200
Participants Needed
1
Research Sites
97 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective is to explore the potential short and long-term impact of the EXOPULSE Mollii Suit and EXOPULSE Suit on subjects with CP, MS, stroke, fibromyalgia or other neurologic disorders which may cause such types of symptoms, and to identify high responders among the sub-categories of the diagnoses. The primary endpoint will be improvements in the Berg/Pediatric Balance Scale (BBS/PBS) as a measurement of balance and risk of falls.
CONDITIONS
Official Title
The EXOPULSE Study - a Database for Routine Follow-up of Clinical Outcomes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with cerebral palsy, multiple sclerosis, stroke, fibromyalgia, or other neurologic disorder causing similar symptoms
- Diagnosis made more than 6 months prior for MS or stroke, or more than 1 month prior for fibromyalgia
- Provided written informed consent
- Cognitively able to understand and follow verbal and/or written instructions
- At least 2 years old
You will not qualify if you...
- Any contraindications listed in the instructions for use of the EXOPULSE Mollii Suit or EXOPULSE Suit
- Starting new medication affecting neuromuscular activity during the study
- Use of botulinum toxin within 3 months before or during the study
- Height less than 100 cm and weight less than 13 kg
- Height over 205 cm and weight over 115 kg
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ottobock Care Sverige
Bergshamra, Stockholm County, Sweden, 170 73
Actively Recruiting
Research Team
M
Milana Mileusnic, PhD
CONTACT
S
Sanna Dünesius, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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