Attainment of Person-centred Goals After Botulinum Toxin Treatment for Upper Limb Spasticity in Real Life Practice

Status:	Active, not recruiting
Conditions:	Neurology
Therapuetic Areas:	Neurology
Healthy:	No
Age Range:	18 - Any
Updated:	1/9/2019
Start Date:	January 2015
End Date:	May 2019

An International, Multicentre, Observational, Prospective, Longitudinal Cohort Study to Assess the Impact of Integrated Upper Limb Spasticity Management Including the Use of BoNT-A- Injections on Patient-centred Goal Attainment in Real Life Practice

The primary purpose for this study is to understand the effect of botulinum toxin as a
treatment integrated in the management of spasticity (stiffness) in the arm and/or hand,
arising from any neurological condition. The study will look at the types of goals that
people choose for treatment, and the extent to which these are achieved in different
individuals.

Inclusion Criteria:

- Adult patients with ULS, in whom a decision has already been made to inject botulinum
toxin A (BoNT A).

- Patient has provided written informed consent for collection of the data.

Exclusion Criteria:

- Participation in any interventional clinical study of ULS within the 12 weeks prior to
the inclusion visit (Visit 1).

- Patient has already been included in the current study, but was subsequently
withdrawn.

We found this trial at

sites

Vanderbilt University

2201 West End Ave
Nashville, Tennessee 37232

(615) 322-7311