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phil,
i am interested in learning more about this study, live in the dc area
so travel is not a great problem.  However, i was recently diagnosed
with msa. fortunately i am in the 25% who responds to parkinson's
medication.  would i be elegablle for this study?

thank you.
cathy  52/dx pd 47/dx msa 52


Phil Gesotti wrote:
>
> As some of you know, I have been working on a non-invasive device to
> relieve PD symptoms. Our recruitment poster is now approved and I am
> authorized to post it on this forum. It is essentially a tactile cueing
> device that I have found effective in relieving my sympotoms. The next
> stage is to determine how effective it can be for other patients.
>
> Phil Gesotti 52/dx 46
> ***************************************************************************
>
> Volunteers with Parkinson's disease needed to test effects of a physical
> device on motor symptoms
> In conjunction with Lockheed Martin Corporation and NIH, doctors at the
> Johns Hopkins University School of Medicine are seeking volunteer
> patients with Parkinson's disease (PD) who experience "freezing" or
> start hesitation to participate in a clinical trial to assess the
> effects of a physical device on the motor symptoms of PD.
>
> Detailed ad:
> PD patients needed for clinical trial of a physical device for symptoms
> of PD
> Volunteers are needed for a clinical trial to test whether a device,
> referred to as a Transcutaneous Electrical Movement Timing Stimulator
> (TEMTS), improves the motor symptoms of Parkinson's disease (PD),
> including bradykinesia (slowed movements), akinesia (inability to
> initiate movements), rigidity, and tremor.  The TEMTS device was modeled
> after a transcutaneous electrical nerve stimulation (TENS) unit, a safe
> and commonly used device to treat pain symptoms.  The TEMTS used in this
> trial is a lightweight portable battery-operated machine (<2 pounds)
> that is inserted into a pouch attached to a belt and worn around the
> waist.  The device provides alternating pulses of low-level stimulation
> to cutaneous electrodes that are placed on the skin over a given
> extremity according to the task performed.  The purpose of this clinical
> trial is to test the effects of the TEMTS device on quantified measures
> of motor initiation, speed, tremor, and tone.
>
> This clinical trial will be limited to patients who experience
> disruptive slowness of movement or difficulty initiating movements (also
> known as "freezing" or start hesitation).   In addition, participants
> must be over age 20 (male or female), have a diagnosis of mild to
> moderately severe PD (Hoehn and Yahr stage II-IV), be on a stable
> regimen of antiparkinsonian medications, and not experience disabling
> memory impairment.   Subjects with a pacemaker or brain-stimulating
> device are not eligible for the study.
>
> The study will take place at Johns Hopkins Hospital and will require
> about 4 hours of testing.  The testing can take place over two separate
> days.  Participants will be provided free parking and compensated $20
> for their time and the costs of traveling to Johns Hopkins.  If you are
> interested in participating, please contact Melissa Gerstenhaber, R.N.,
> M.S.N., Research Nurse Coordinator for the Morris K. Udall Parkinson's
> Disease Research Center of Excellence at Johns Hopkins (410-614-1242) or
> email her at [log in to unmask]  The principal investigator of this
> study is Laura Marsh, M.D..  Lockheed Martin Corporation and the
> National Institutes of Health are providing financial support for the
> study.
>
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