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Clinical Trials/NCT01317303
NCT01317303
Completed
Not Applicable

Comparison of Measures of Plasticity

The University of New South Wales1 site in 1 country16 target enrollmentMarch 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
The University of New South Wales
Enrollment
16
Locations
1
Primary Endpoint
amplitude of motor evoked potentials
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Neuroplasticity refers to the ability of the nerve cells to modify their structure or function in response to injury or insult, or other environmental stimuli, with these changes outlasting the period of exposure. Plasticity may be observed as short term or long term changes. In humans, neuroplasticity can be readily assessed in the motor cortex, as excitability changes are demonstrated in the degree to which peripheral muscles are activated, seen through changes in motor-evoked potentials (MEPs). In this study, a number of approaches to assessing neuroplasticity will be evaluated: Paired-associative stimulation (PAS), Theta Burst Stimulation (TBS), which is a form of transcranial magnetic stimulation (TMS) and protocols that combine these two. In addition, participants will complete a computerised 'rotor pursuit task' designed to provide a measure of motor learning.

The investigators aim to find the most efficacious (defined by greatest number of responders and effect size as seen in an increase in MEP amplitude) brain stimulation protocol. The investigators will expose the same participants to four excitatory conditioning stimulation paradigms, with each session separated by at least a week.

Our hypotheses include:

The four conditioning stimulation protocols should increase motor cortical excitability, the investigators therefore expect there to be a significant increase in participant MEPs, with a positive correlation in the increase ofMEP amplitude of the protocols. The investigators do however expect that due to the principles of homeostatic metaplasticity, that the protocols preceded by cTBS will show greater MEP change, due to the lowering of the threshold for LTP plasticity induction. In addition, the investigators expect that an increase in the motor learning manifest by the rotor pursuit task and for there to be a correlation in participants between the increase in MEP amplitude and the improvement in time on target (TOT) shown in the motor learning task (MLT).

Registry
clinicaltrials.gov
Start Date
March 2011
End Date
November 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Colleen Loo

Professor

The University of New South Wales

Eligibility Criteria

Inclusion Criteria

  • healthy controls
  • those suffering depression

Exclusion Criteria

  • Significant Neurological illness, including epilepsy
  • Alcohol use above NHRMC guidelines
  • Illicit drug use
  • Electronic implant; such as cochlear implant or pacemaker
  • Musculoskeletal disorder

Outcomes

Primary Outcomes

amplitude of motor evoked potentials

Time Frame: 60 minutes post brain stimulation protocol intervention

Secondary Outcomes

  • motor learning through performance on a 'rotor pursuit task'(time frame relates to 5 blocks of 5 trials for each participant)

Study Sites (1)

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