Evaluation of Long-term Effect of Resonator Therapy on Parkinson's Disease (PD)
Primary Purpose
Parkinson's Disease
Status
Completed
Phase
Locations
Study Type
Observational
Intervention
Resonator Device
Sponsored by
About this trial
This is an observational trial for Parkinson's Disease
Eligibility Criteria
Inclusion Criteria:
- Prior participation in pico-tesla pilot studies: NCT00779155 & NCT00863226
- Willing and able to abstain from partaking in non-essential new treatments for Parkinson's disease symptoms during the course of participation of the study.
- Will and able to abstain from all non-essential new medications that could affect PD and/or any of its associated symptoms for the duration of the study.
- Willing to notify the investigator right away of any changes in medication use or therapies that is prescribed and deemed necessary by the subjects physicians.
- Adequate contraceptive measures for female subjects
- Capable of giving full written informed consent
Exclusion Criteria:
- Not a participant in IRC#'s 07102 or 07021
- No active brain tumors, strokes, hydrocephalus
- Chronic pain not associated with PD
- Any other condition which might prevent subject from comfortably sitting for 1.5 hours
- Consumption of medications that can produce Parkinsonism type symptoms
- Major psychiatric disturbance
- Epilepsy
- HIv and other autoimmune disorders
- Cancer within last 2 years
- History of ECt
- Diabetic neuropathy
- Uncontrolled HTN
- Advanced Pulmonary disease
- Known heart conditions such as repetitive history of cardiac arrythmias
- Previous surgeries for PD
- Prosthetics comprised of ferrous materials
- Stents, only where there is also cardiac arrythmias, CHF, advanced valvular stenosis, unstable vital signs, extensive ischemic damage to heart muscle as a result of one or more heart attacks.
- Pacemakers
- Uncontrolled, unstable, or untreated medical illnesses which might potentially significantly affect the patient's health in the opinion of the investigator
- Consumption of more than 21 alcoholic drinks per week
- Pregnant, breast feeding or planning pregnancy
- Developmental disability or cognitive impairment
- Inability to maintain regular medication regime
- Inability to abstain from partaking in new non-essential PD tx., or medications
- Not willing to report physician mandated changes in medication and/or treatment
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Arm Label
Active Resonator magnetic field therapy
Arm Description
Administration of active magnetic fields with the Resonator Device
Outcomes
Primary Outcome Measures
Change in Parkinson's Disease Questionnaire-39 Single Index Score (PDQ-39SI)From Baseline to Study Endpoint of 11 Months
The Parkinson's Disease Questionnaire (PDQ-39) is a 39-item quality of life questionnaire for patients with Parkinson's Disease (PD) that evaluates the 8 dimensions of mobility, activities of daily living, emotional well-being, stigma, social support, cognition, and communication. The PDQ-39 Single Index (SI) score is the weighted addition of scores on all 8 dimension and ranges from 0 (no disease impact) to 100 (severe disease impact).
Secondary Outcome Measures
Full Information
NCT ID
NCT00862537
First Posted
October 22, 2008
Last Updated
June 9, 2011
Sponsor
pico-tesla Magnetic Therapies, LLC
1. Study Identification
Unique Protocol Identification Number
NCT00862537
Brief Title
Evaluation of Long-term Effect of Resonator Therapy on Parkinson's Disease (PD)
Official Title
An Open-label Extension Study for Subjects Previously Treated Either in Pilot I or Pilot II Studies of the Application of Magnetic Fields Using the Resonator for the Treatment of Parkinson's Disease.
Study Type
Observational
2. Study Status
Record Verification Date
June 2011
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
April 2011 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
pico-tesla Magnetic Therapies, LLC
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
An extension study for subjects with prior participation in previous resonator studies using low level magnetic fields to treat some of the symptoms of idiopathic Parkinson's Disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease
7. Study Design
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Active Resonator magnetic field therapy
Arm Description
Administration of active magnetic fields with the Resonator Device
Intervention Type
Device
Intervention Name(s)
Resonator Device
Intervention Description
active pico-tesla magnetic fields treatment for Parkinson's disease individuals
Primary Outcome Measure Information:
Title
Change in Parkinson's Disease Questionnaire-39 Single Index Score (PDQ-39SI)From Baseline to Study Endpoint of 11 Months
Description
The Parkinson's Disease Questionnaire (PDQ-39) is a 39-item quality of life questionnaire for patients with Parkinson's Disease (PD) that evaluates the 8 dimensions of mobility, activities of daily living, emotional well-being, stigma, social support, cognition, and communication. The PDQ-39 Single Index (SI) score is the weighted addition of scores on all 8 dimension and ranges from 0 (no disease impact) to 100 (severe disease impact).
Time Frame
baseline and 11 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
82 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Prior participation in pico-tesla pilot studies: NCT00779155 & NCT00863226
Willing and able to abstain from partaking in non-essential new treatments for Parkinson's disease symptoms during the course of participation of the study.
Will and able to abstain from all non-essential new medications that could affect PD and/or any of its associated symptoms for the duration of the study.
Willing to notify the investigator right away of any changes in medication use or therapies that is prescribed and deemed necessary by the subjects physicians.
Adequate contraceptive measures for female subjects
Capable of giving full written informed consent
Exclusion Criteria:
Not a participant in IRC#'s 07102 or 07021
No active brain tumors, strokes, hydrocephalus
Chronic pain not associated with PD
Any other condition which might prevent subject from comfortably sitting for 1.5 hours
Consumption of medications that can produce Parkinsonism type symptoms
Major psychiatric disturbance
Epilepsy
HIv and other autoimmune disorders
Cancer within last 2 years
History of ECt
Diabetic neuropathy
Uncontrolled HTN
Advanced Pulmonary disease
Known heart conditions such as repetitive history of cardiac arrythmias
Previous surgeries for PD
Prosthetics comprised of ferrous materials
Stents, only where there is also cardiac arrythmias, CHF, advanced valvular stenosis, unstable vital signs, extensive ischemic damage to heart muscle as a result of one or more heart attacks.
Pacemakers
Uncontrolled, unstable, or untreated medical illnesses which might potentially significantly affect the patient's health in the opinion of the investigator
Consumption of more than 21 alcoholic drinks per week
Pregnant, breast feeding or planning pregnancy
Developmental disability or cognitive impairment
Inability to maintain regular medication regime
Inability to abstain from partaking in new non-essential PD tx., or medications
Not willing to report physician mandated changes in medication and/or treatment
Study Population Description
Previous participants enrolled in one of two prior pico-tesla Magnetic Therapies Resonator device studies using magnetic fields for treating Parkinson's Disease (PD) symptoms.
Sampling Method
Non-Probability Sample
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jerry I Jacobson, PhD., DMD.
Organizational Affiliation
pico-tesla Magnetic Therapies, LLC
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Evaluation of Long-term Effect of Resonator Therapy on Parkinson's Disease (PD)
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