Spasticity is a common consequence of injury to the central nervous system and can be a major problem in motor function and everyday activities. A method for treating spasticity that applies low-amplitude electrical stimulation through a garment with built-in electrodes, Mollii® (Elektrodress), has been developed. The garment is to be used in combination with individualized training and the stimulation is mainly given to antagonists of spastic muscles. The general objective of this study is to evaluate the efficacy of and costs associated with the Mollii® treatment of spasticity due to stroke or cerebral palsy. Primary objectives are; * to study whether treatment with the Mollii® improves function and activity * to evaluate the cost-effectiveness of the treatment, from both a health-care perspective and a societal perspective. Secondary objectives are; * to study whether there are differences in treatment effect between the stroke and the Cerebral Palsy groups in a subgroup-analysis * to assess compliance with treatment * to report any adverse effects.
This study is designed as a double-blinded, randomized, cross-over trial (RCT). This part of the study takes 12 weeks (6 weeks of active treatment and 6 weeks of non-active treatment) and is followed by a wash-out period of 6 weeks. An uncontrolled,open phase starts after week 18, where patients are followed one year after inclusion. 30 participants with spasticity due to Stroke and Cerebral Palsy will be included. Two centers are recruiting participants and are collecting data. Outcome measures are chosen to reflect the different dimensions in the International Classification of Functioning, Disability and Health (ICF) and patient reported outcome measures (PROM).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
31
Multifocal transcutaneous electrical stimulation incorporated into a whole-body garment in combination with training
Goal attainment scaling (GAS)
1 to 3 goals are defined and evaluated using the original GAS scale by Kiresuk
Time frame: 12 weeks
Arm-hand ability (ARAT + WMFT tasks 1&2)
Action Research Arm Test (ARAT)measuring grasp, grip, pinch and gross movement and this is complemented by Wolf Motor Function Test (WMFT) tasks 1 and 2 measuring active shoulder abduction
Time frame: 12 weeks
Mobility
10 meter walking test, divided into comfortable gait test (CGT) and fast gait test (FGT). Outcome is velocity, cadence and stride length. Timed Up \& Go (TUG)
Time frame: 12 weeks
Health related Quality of Life/QALY
SF-36 and EQ-VAS
Time frame: Baseline, week 6, 12, 18, 52
Self reported pain and spasticity
Numeric rating scale (NRS)
Time frame: Baseline, week 6, 12, 18, 52
Muscle hypertonicity (Spasticity)
Modified Ashworth scale (0-5)
Time frame: Baseline, week 6, 12, 18, 52
Range of Motion
Goniometer
Time frame: Baseline, week 6, 12, 18, 52
Costs
Costs directly related to intervention Baseline, week 6, 12, 18 Costs from a societal perspective at baseline and week 52
Time frame: Baseline, week 6, 12, 18, 52
Goal Attainment Scaling (GAS)
1 to 3 goals are defined and evaluated using the original GAS scale by Kiresuk
Time frame: 52 weeks
Arm-hand ability (ARAT + WMFT tasks 1&2)
Action Research Arm Test (ARAT)measuring grasp, grip, pinch and gross movement and this is complemented by Wolf Motor Function Test (WMFT) tasks 1 and 2 measuring active shoulder abduction
Time frame: 52 weeks
Mobility
10 meter walking test, divided into comfortable gait test (CGT) and fast gait test (FGT). Outcome is velocity, cadence and stride length. Timed Up \& Go (TUG)
Time frame: 52 weeks
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