Clinical Trials Directory

Trials / Completed

CompletedNCT02261142

Efficacy and Cost-effectiveness of Spasticity Treatment With Multifocal TENS

Evaluation of Efficacy and Cost-effectiveness of Spasticity Treatment With Multifocal Transcutaneous Electrical Stimulation, Through a Garment With built-in Electrodes in Combination With Training.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Linkoeping University · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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).

Conditions

Interventions

TypeNameDescription
DEVICEMultifocal TENS garment (Mollii®)Multifocal transcutaneous electrical stimulation incorporated into a whole-body garment in combination with training

Timeline

Start date
2013-09-01
Primary completion
2015-02-01
Completion
2015-02-01
First posted
2014-10-10
Last updated
2015-07-13

Source: ClinicalTrials.gov record NCT02261142. Inclusion in this directory is not an endorsement.