Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
24 participants
INTERVENTIONAL
2007-05-31
2008-07-31
Brief Summary
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The goal of our research is to improve dystonia symptoms in patients with hand dystonia. We will attempt to achieve this goal by implementing an intensive training treatment that requires patients to attend to, and use touch information applied to specific fingertips. Previous work has attempted to alter touch perception using sensory training and improvements in motor control (hand writing) of dystonia patients were observed. For example, learning to read Braille improves tactile perception and handwriting in focal hand dystonia. A different approach to treat focal hand dystonia involves a technique called repetitive transcranial magnetic stimulation (rTMS), and this can also temporarily improve hand writing in dystonia patients. The proposed research will attempt to alter touch processing using touch training alone, or in combination with rTMS. Rather than train using Braille reading, the sensory training will be applied using a systematic, experimenter controlled stimulus set that focuses on touch stimuli applied to individual digits. Importantly patients will have to associate certain types of touch information with rewards and other touch input with the lack of a reward.
The study will first involve measuring the location and representation of the touch in the brain using multiple brain mapping tools. These tools include functional magnetic resonance imaging and magnetoencephalography; when both tools are used a very accurate picture of finger representation can be obtained, and we also know what brain areas respond to touch stimuli. Dystonia symptoms and touch perception will also be assessed. Next, patients will participate in a training intervention that involves 15 days(2.5 hr/day) of touch training applied to the fingertips of the dystonia affected hand. Patients will identify the touch targets amongst distractors and receive on-line performance feedback. The goal of the training is to provide the cortex with regular boundaries of fingers and in this way, attempt to re-shape the sensory cortex to accept these boundaries. Another group of patients will receive rTMS. The goal of the rTMS is to create an environment in sensory cortex that is open or 'ready' to accept changes induced by tactile stimulation. The rTMS will be immediately followed by the tactile training. A third group of patients will receive a placebo version of rTMS followed by tactile training. The latter group will allow us to understand if rTMS has a definite effect on the physiology of the patient. Following the 15-day training, we will assess the brains representation of fingertips, changes in dystonia symptoms and changes in the perception of touch stimuli.
This research will advance the treatment of focal hand dystonia and assist the design of precise remediation training tailored to the dystonia patient.
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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1
Tactile training + sham rTMS
tactile training for 2.5/hr/day for 15 days - this plus the sham rTMS
2
Tactile training + rTMS
tactile training 2.5/hr/day for 15 days plus daily 5Hz rTMS
Interventions
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Tactile training + sham rTMS
tactile training for 2.5/hr/day for 15 days - this plus the sham rTMS
Tactile training + rTMS
tactile training 2.5/hr/day for 15 days plus daily 5Hz rTMS
Eligibility Criteria
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Inclusion Criteria
* Writer's cramp,
* Musician's cramp,
* Dystonic cramp.
Exclusion Criteria
* Epilepsy
* Carpal tunnel or disorders of peripheral nerves
* Psychiatric illness
18 Years
ALL
No
Sponsors
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Dystonia Medical Research Foundation
OTHER
University Health Network, Toronto
OTHER
Responsible Party
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Toronto Western Research Institute, University of Waterloo
Principal Investigators
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Aimee J Nelson, PhD
Role: PRINCIPAL_INVESTIGATOR
Toronto Western Research Institute, University of Waterloo
Locations
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Toronto Western Hosptial
Toronto, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Aimee J Nelson, PhD
Role: primary
Carolyn Gunraj, MSc
Role: backup
Other Identifiers
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05-0959-A
Identifier Type: -
Identifier Source: secondary_id
05-0959-A
Identifier Type: -
Identifier Source: org_study_id