Mollii - Personalized Suit for Treatment of Spasticity, GFMCS 3-5

Status Completed

Clinical Trial Summary

The objective of this study was to examine the effect on spasticity and function of multifocal transcutaneous electrical stimulation incorporated in a 2-piece (Mollii) suit.

Clinical Trial Description

In this prospective cohort study, the participants (children with predominantly spastic CP, GFMCS 3-5) wore the suit for 1 hour every second day for 24 weeks. The investigators evaluated level of spasticity using the modified Ashworth scale (MAS) and other related measures before initiation, after 4, 12, and 24 weeks. Two motor related smart goals were defined and evaluated by the goal attainment scale (GAS). GMFM-66 and posture and postural ability scale (PPAS) were performed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04322825
Study type	Interventional
Source	Hvidovre University Hospital
Contact
Status	Completed
Phase	N/A
Start date	June 1, 2017
Completion date	July 1, 2019

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