Somatosensory Processing in Focal Hand Dystonia

NCT ID: NCT00579033

Last Updated: 2007-12-21

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-05-31

Study Completion Date

2008-07-31

Brief Summary

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Patients with focal dystonia experience uncontrollable movements of the hand during certain types of skilled movements. Though the origin of the disorder is not fully understood, it is thought that brain areas involved in moving the hands and receiving touch information from the hands, are involved. For example, patients with dystonia affecting the hand show changes in their ability to perceive touch - this is something that typically escapes the patients own awareness. Further, the area of the brain receiving touch information has a disrupted representation of the finger skin surfaces.

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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Focal Hand Dystonia Musician's Dystonia Writer's Cramp Dystonic Cramp

Keywords

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somatosensory cortex neuroimaging tactile cortical plasticity dystonia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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1

Group Type SHAM_COMPARATOR

Tactile training + sham rTMS

Intervention Type OTHER

tactile training for 2.5/hr/day for 15 days - this plus the sham rTMS

2

Group Type ACTIVE_COMPARATOR

Tactile training + rTMS

Intervention Type OTHER

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

Intervention Type OTHER

Tactile training + rTMS

tactile training 2.5/hr/day for 15 days plus daily 5Hz rTMS

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of focal hand dystonia including any but not limited to the following:

* Writer's cramp,
* Musician's cramp,
* Dystonic cramp.

Exclusion Criteria

* Other neurological conditions
* Epilepsy
* Carpal tunnel or disorders of peripheral nerves
* Psychiatric illness
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dystonia Medical Research Foundation

OTHER

Sponsor Role collaborator

University Health Network, Toronto

OTHER

Sponsor Role lead

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

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Aimee J Nelson, PhD

Role: CONTACT

Phone: 416-603-5792

Email: [email protected]

Robert Chen, MD

Role: CONTACT

Phone: 416-603-5424

Email: [email protected]

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