The primary objective of this study is to establish whether cerebellar patient populations can adapt and learn to maintain standing balance when sensory-motor relationships of balance are modified. By comparing patient behavior with age-matched…
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Source
Brief title
Condition
- Other condition
Synonym
Health condition
sensorimotor learning for standing balance in cerebellar patients
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameters are measures of standing balance behaviour (whole
body kinematics and kinetics) and evoked balance responses (probed with sensory
and/or mechanical stimuli).
Secondary outcome
Healthy controls and cerebellar patient participants will be asked to visit the
Department of Neuroscience at Erasmus at least one time for the selected
experiment. During the visit, they will perform tasks specific to each
experiment. The robotic balance simulator does not present significant
discomfort or risk for the participants.
Background summary
Recent studies have provided insights into the capabilities and mechanisms of
sensorimotor adaptation and learning in human standing balance. These include
establishing the underlying mechanisms for the nervous system to recalibrate to
novel sensory feedback, adjust control when sensory-motor relationships change,
and learn to maintain standing under conditions which are initially
destabilizing. However, it remains largely unclear which neural structures are
responsible for these adaptive learning processes. A candidate brain region is
the cerebellum, given its roles in multisensory integration and sensorimotor
prediction, though several questions regarding its involvement in adaptive
learning remain unanswered. What types of adaptive processes in standing
balance control does the cerebellum contribute to? If cerebellar function is
compromised, can other parts of the nervous system accommodate for the
dysfunction and facilitate sensorimotor learning? And if possible, under what
sensorimotor conditions can this be achieved? With the research proposed here,
we seek to understand whether compromised cerebellar function impairs
sensorimotor adaptation and learning in human standing balance. Furthermore, we
seek to determine what sensory feedback conditions are optimal for cerebellar
patients to adapt and learn new balance tasks.
Study objective
The primary objective of this study is to establish whether cerebellar patient
populations can adapt and learn to maintain standing balance when sensory-motor
relationships of balance are modified. By comparing patient behavior with
age-matched control participants, we will determine whether disrupted
cerebellar function impedes the sensorimotor learning processes involved in
standing balance.
Study design
All experiments will involve healthy controls and cerebellar patients
performing standing balance experiments on a robotic balance simulator. This
simulator is used to control, replicate, and modify the mechanics and
sensory-motor relationships for ongoing standing.
Study burden and risks
Healthy participants will visit the Erasmus MC at least once (up to 2 times)
and an experiment will last for a maximum of 2 hours. The total time spent
testing a subject will be limited to 4 hours regardless of experimental
protocol. In this study, the safety measures are applied as described in recent
human balance and sensory stimulation reviews. There are no serious risks
associated with this study. The discomfort and risks associated with the
experiments described in this proposal are minor but vary according to the
methods used for each experiment. The risks/discomfort for the various
techniques used are provided below.
Robotic balance simulator
Standing in the robotic balance simulator may cause vertigo and nausea for
participants who are particularly subject to those complaints. When a subject
indicates vertigo and/or nausea during any experiment and indicates that they
wish to end the experiment, this request will be granted immediately.
Dr. Molewaterplein 40
Rotterdam 3015 GD
NL
Dr. Molewaterplein 40
Rotterdam 3015 GD
NL
Listed location countries
Age
Inclusion criteria
For healthy controls:
• In overall good health
• Age: 18 - 90 years old
For patients:
• Adults between the age of 18 - 90 years old who have been diagnosed with a
cerebellar lesion.
• Patients will be invited to participate in the study within 3-12 months after
their initial diagnosis.
Exclusion criteria
For healthy controls:
• History of neurological or psychiatric disorders
• Taking acute or chronic psychoactive drugs
• Alcoholism
• History of balance problems
• Pregnant women or women currently breastfeeding
• A prior neuromuscular injury (regardless of source)
• Incompetence to give informed consent
For patients:
• Unable to walk 10 metres unaided
• Unable to stand freely for 10 seconds with the eyes closed
• Diagnosed with polyneuropathy
• Taking acute or chronic psychoactive drugs
• Alcoholism
• Pregnant women or women currently breastfeeding
• Incompetence to give informed consent
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL81081.078.22 |