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ABSTRACT: Background
Both prolonged-release fampridine (PRF) and enabling active motor training (EAMT) are beneficial in multiple sclerosis (MS) patients. Their combined effect is, however, understudied.Objective
The objective of this paper is to determine if PRF augments the beneficial effect of EAMT in MS patients as opposed to placebo.Method
This is a pilot, randomized, placebo-controlled, double-blind 14-week study. Participants were randomly assigned to receive PRF 10 mg BID (n = 21) or placebo (n = 20). All patients underwent EAMT during the first six weeks. Patients were assessed at -4, 0, 6 and 14 weeks.Results
Both groups remained stable between -4 to 0 weeks and showed statistically significant improvements for the six-minute walk and the five-times-sit-to-stand test at weeks 6 and 14. The PRF-treated group achieved a greater mean percentage improvement and a higher incidence of responders in all three tasks at both time points. The study was, however, underpowered to reach statistical significance.Conclusion
Our results confirm previous studies demonstrating that MS patients, despite significant disability, do benefit from a rehabilitation program. Our study is the first to show a trend suggesting that PRF in MS patients appears to enhance the benefit of EAMT. Further studies are required to confirm this.Clinical trial registration number with Clinicaltrial.gov: NCT02146534.
SUBMITTER: Jacques F
PROVIDER: S-EPMC5846958 | biostudies-literature | 2018 Jan-Mar
REPOSITORIES: biostudies-literature
Jacques François F Schembri Adrian A Nativ Avi A Paquette Chantal C Kalinowski Pawel P
Multiple sclerosis journal - experimental, translational and clinical 20180101 1
<h4>Background</h4>Both prolonged-release fampridine (PRF) and enabling active motor training (EAMT) are beneficial in multiple sclerosis (MS) patients. Their combined effect is, however, understudied.<h4>Objective</h4>The objective of this paper is to determine if PRF augments the beneficial effect of EAMT in MS patients as opposed to placebo.<h4>Method</h4>This is a pilot, randomized, placebo-controlled, double-blind 14-week study. Participants were randomly assigned to receive PRF 10 mg BID ( ...[more]