Mollii Suit 60-minute trial in people with a Spinal Cord Injury
- Conditions
- Spinal cord injuryspasticityNeurological - Other neurological disordersPhysical Medicine / Rehabilitation - Other physical medicine / rehabilitationInjuries and Accidents - Other injuries and accidents
- Registration Number
- ACTRN12622000223730
- Lead Sponsor
- euroscience Research Australia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Participants will be included if they:
•have spinal cord injury
•have spasticity, defined as scoring at least 1 on the Modified Tardieu Scale
•are able to perform the Timed Up and Go test
•do not have implanted devices (e.g. pacemaker, Baclofen pump)
Participants will not be included if they:
•have a history of clinically significant autonomic dysreflexia in response to electrical stimulation
•have a history of hypotension in response to prolonged standing
•have a history of long-bone fracture, family history of fragility fracture or any disorders of the bone, such as Paget’s disease that prevents standing for up to 60 minutes
•have extensive lower limb contractures (limiting ROM by at least 30% within normal ranges required for ambulation)
•have any contraindications to electrical stimulation such as cardiac pacemaker, baclofen pump, pregnancy, or hardware near the stimulation site
•are actively participating in any other clinical trials or are still in the follow-up period of a clinical trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to complete the Timed Up and Go test will assess participants functional strength, balance and mobility. A chair of standard height and a digital stop watch will be used in this assessment.[ 2 weeks post-intervention commencement]
- Secondary Outcome Measures
Name Time Method