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Clinical Trial Summary

The aim of this study is to investigate two different modalities of functional electrical stimulation (FES) leg exercise in patients with spinal cord injury (SCI). The primary outcomes being compared are 1. FES-induced leg aerobic fitness, and 2. FES-induced leg strength. There will be two FES-leg training groups, and sub-acute patients with SCI will be randomised between the groups - high-short [HI-SHORT] and low-long [LO-LONG]. Both groups (n=10 per group) will exercise on the Hasomed RehaStimâ„¢ exercise ergometer for 6-8 weeks, three-four times per week (24 therapy sessions). [HI-SHORT] will perform 10 x 2-min of high-intensity interval training with a recovery of 1-2 min between exercise bouts. [LO-LONG] will perform 20+ min of continuous exercise at a low-moderate exercise intensity. Exercise intensity for [HI-SHORT] and [LO-LONG] will be titrated by neuromuscular stimulation characteristics. The primary outcomes will be assessed before training commences and after 6-8 weeks of training has been completed.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03621254
Study type Interventional
Source Swiss Paraplegic Research, Nottwil
Contact Glen M Davis, PhD
Phone +41 41 939 42 06
Email ines.bersch@paraplegie.ch
Status Recruiting
Phase N/A
Start date January 7, 2019
Completion date December 2024

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