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Transcranial Electrical Polarization to Treat Focal Hand Dystonia

Primary Purpose

Dystonia, Focal Hand Dystonia, FHD

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Transcranial Electrical Polarization (TEP)
Sponsored by
National Institute of Neurological Disorders and Stroke (NINDS)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dystonia focused on measuring Electrical, Stimulation, Dystonia, Brain, Focal Hand Dystonia, FHD

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA: Subjects with focal hand dystonia 18 years old or older will be included. EXCLUSION CRITERIA: Exclusion criteria will include the standard exclusions for TEP as well as exclusions specific to this study. We will exclude subjects with: Any significant medical or psychiatric illness (other than FHD). Patients with a positive pregnancy test will be excluded because the effects of TEP on the fetus is unknown. A urine sample for pregnancy testing will be obtained prior to the TEP, and on the day of the first TEP session. History of epilepsy. Concurrent use of neuroleptic agents. Any other licit or illicit drugs other that could lower the seizure threshold. Metal implants. Who have received botulinum toxin injection within 10 weeks of starting the protocol. Secondary hand dystonia. Mentally impaired patients having no capacity to provide their own consent will be excluded from the study because such patients may have difficulty performing the required test. If participation in the study would, in the opinion of the investigators, cause undue risk or stress for reasons such as excessive fatigue, general frailty, or excessive apprehension. Unable or unwilling to refrain from alcohol for 24 hours prior to study days. Patients may continue taking muscle relaxants, artane and other anticholinergic drugs, L-DOPA and dopamine agonists.

Sites / Locations

  • National Institutes of Health Clinical Center, 9000 Rockville Pike

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

1

2

Arm Description

Real TEP

Sham Stimulation

Outcomes

Primary Outcome Measures

The Fahn Dystonia Scale before and after real and placebo TEP course.

Secondary Outcome Measures

Full Information

First Posted
March 29, 2005
Last Updated
June 30, 2017
Sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
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1. Study Identification

Unique Protocol Identification Number
NCT00106782
Brief Title
Transcranial Electrical Polarization to Treat Focal Hand Dystonia
Official Title
Placebo Controlled Study of the Therapeutic Effect of the Transcranial Electrical Polarization in Patients With Focal Hand Dystonia
Study Type
Interventional

2. Study Status

Record Verification Date
May 14, 2010
Overall Recruitment Status
Completed
Study Start Date
March 18, 2005 (undefined)
Primary Completion Date
May 14, 2010 (Actual)
Study Completion Date
May 14, 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Neurological Disorders and Stroke (NINDS)

4. Oversight

5. Study Description

Brief Summary
This study will evaluate the effect of transcranial electrical polarization (TEP), also called direct current (DC) stimulation, on focal hand dystonia in people with writer's cramp. In dystonia, muscle spasms cause uncontrolled twisting and repetitive movement or abnormal postures. Focal dystonia involves just one part of the body, such as the hand, neck or face. When people with focal hand dystonia make small and repeated movements with their hands, there is extra activity in the part of the brain called the motor cortex. TEP is a method of brain stimulation that slows down the activity of the nerve cells in the motor cortex. This study may help researchers develop new ways to treat focal hand dystonia. People 18 years of age and older with focal hand dystonia may be eligible for this study. Participants have a neurological examination and are randomly assigned to one of two treatment groups: TEP or placebo stimulation. The TEP group receives stimulation to the parts of the brain used for hand movement, and the placebo group receives sham stimulation, which does not affect any area of the brain. There are three TEP/placebo sessions over a period of 7 to 10 days. The first session may last up to 2-1/2 hours; the other two sessions last 1-2 hours. For TEP, sponge electrodes are placed on the scalp and an electrical current is passed through the scalp and skull to the outer part of brain. Before and after each session, participants have a neurological examination, including an evaluation of the rate and severity of their movement problems. For this assessment, participants do a writing test while the electrical activity of their hand muscles is recorded using surface electromyography (EMG). For EMG, small metal disks (electrodes) filled with a conductive gel are taped to the skin over the muscles being tested. Patients are followed in the clinic the day after the end of TEP treatment for evaluation of their movement abilities and the effects of therapy, such as improvement of handwriting.
Detailed Description
Objective: The treatment of focal hand dystonia (FHD) needs further improvement. A deficiency of inhibition was demonstrated in patients with writer's cramp. The passage of weak DC currents across the head, or transcranial electrical polarization (TEP) has been done for many years with numerous effects described in healthy subjects and mentally diseased patients. Recently, it has been shown by objective means, in controlled experiments, that this type of treatment has robust and lasting effects on the excitability of the motor cortex in healthy humans. Study population: 40 subjects with focal hand dystonia. Design: We hypothesize that TEP will have a beneficial effect on hand writing in patients with FHD because it will decrease the excitability of the motor cortex compensating the deficiency of inhibition. Specifically, we propose to look at the effect of 2 mA TEP with cathode position over the hand projection in the contralateral to the affected hand primary motor cortex. Anodes will be placed over the orbit and mastoid process ipsilateral to the affected hand (contralateral to the cathode). Over a two-year period, we will enroll 40 patients with FHD and evaluate the acute TEP effects over a period of 1 week (3 TEP sessions). Outcome measures: Symptoms will be evaluated by kinematic analysis of the handwriting and with dystonia scales.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dystonia, Focal Hand Dystonia, FHD
Keywords
Electrical, Stimulation, Dystonia, Brain, Focal Hand Dystonia, FHD

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Other
Arm Description
Real TEP
Arm Title
2
Arm Type
Other
Arm Description
Sham Stimulation
Intervention Type
Procedure
Intervention Name(s)
Transcranial Electrical Polarization (TEP)
Primary Outcome Measure Information:
Title
The Fahn Dystonia Scale before and after real and placebo TEP course.
Time Frame
1 week post-TEP

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: Subjects with focal hand dystonia 18 years old or older will be included. EXCLUSION CRITERIA: Exclusion criteria will include the standard exclusions for TEP as well as exclusions specific to this study. We will exclude subjects with: Any significant medical or psychiatric illness (other than FHD). Patients with a positive pregnancy test will be excluded because the effects of TEP on the fetus is unknown. A urine sample for pregnancy testing will be obtained prior to the TEP, and on the day of the first TEP session. History of epilepsy. Concurrent use of neuroleptic agents. Any other licit or illicit drugs other that could lower the seizure threshold. Metal implants. Who have received botulinum toxin injection within 10 weeks of starting the protocol. Secondary hand dystonia. Mentally impaired patients having no capacity to provide their own consent will be excluded from the study because such patients may have difficulty performing the required test. If participation in the study would, in the opinion of the investigators, cause undue risk or stress for reasons such as excessive fatigue, general frailty, or excessive apprehension. Unable or unwilling to refrain from alcohol for 24 hours prior to study days. Patients may continue taking muscle relaxants, artane and other anticholinergic drugs, L-DOPA and dopamine agonists.
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
3808255
Citation
Agnew WF, McCreery DB. Considerations for safety in the use of extracranial stimulation for motor evoked potentials. Neurosurgery. 1987 Jan;20(1):143-7. doi: 10.1097/00006123-198701000-00030.
Results Reference
background
PubMed Identifier
11733710
Citation
Antal A, Nitsche MA, Paulus W. External modulation of visual perception in humans. Neuroreport. 2001 Nov 16;12(16):3553-5. doi: 10.1097/00001756-200111160-00036.
Results Reference
background
PubMed Identifier
9339689
Citation
Chen R, Wassermann EM, Canos M, Hallett M. Impaired inhibition in writer's cramp during voluntary muscle activation. Neurology. 1997 Oct;49(4):1054-9. doi: 10.1212/wnl.49.4.1054.
Results Reference
background

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Transcranial Electrical Polarization to Treat Focal Hand Dystonia

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