Multiple Sclerosis Clinical Trial
Official title:
A Feasibility Study Monitoring the Respiratory Status of Participants Receiving or Scheduled to Receive Intrathecal Baclofen (ITB)
The methodology is a feasibility study to determine the feasibility of assessing people in the community with a neurological condition before proceeding towards a full powered community trial evaluating the influence of intrathecal baclofen.
The purpose of this proposed research will evaluate a feasible method to assess the
respiratory status of people with neurological conditions receiving or scheduled to receive
Intrathecal Baclofen. The use of Intrathecal Baclofen to manage severe spasticity is a
developing treatment option with a limited research base, particularly when evaluating the
influence of intrathecal baclofen on the respiratory system. The proposed research is derived
from clinical practice and involves joint collaboration between clinical team, research
professionals and patients.
In order for the study to evaluate the influence of Intrathecal baclofen has on the
respiratory system, the proposed research will need to develop and evaluate a method of
assessing people in the community ensuring it's feasible for people with neurological
conditions. Prior to implementing a full powered community trial to evaluate the influence of
intrathecal baclofen on people with neurological conditions.
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