Battery-preserving Stimulation Patterns for Deep Brain Stimulation

Sponsor
University of Florida (Other)
Overall Status
Completed
CT.gov ID
NCT02569021
Collaborator
(none)
30
1
28.1
1.1

Study Details

Study Description

Brief Summary

The purpose of this research study is to test effectiveness of different deep brain stimulation (DBS) stimulation patterns on symptoms that may also improve the life of the battery. If these patterns are effective, the implanted batteries will be drained more slowly and last longer than currently expected. An increase in battery life may reduce the number of surgeries needed to replace them.

Condition or Disease Intervention/Treatment Phase
  • Device: Biphasic DBS stimulation
  • Other: Unified Parkinson's Disease Rating Scale
  • Other: Tremor Rating Scale
  • Device: Kinesia accelerometer
  • Device: Trigno wireless system
  • Other: GaitRite walking assessment.

Detailed Description

Deep brain stimulation (DBS) is an effective surgical therapy for medication-refractory symptoms of Parkinson's disease, tremor, and dystonia. Patients implanted with DBS experience a significant improvement of their symptoms with relatively low risk of intolerable side effects. Implanted patients must undergo repeat surgeries to replace the Implantable Pulse Generators/batteries (IPG) approximately every 2 to 5 years. The DBS program (at the University of Florida) has studied battery consumption and has been interested in potential strategies to extend the life of the IPG to reduce the need for frequent battery replacement surgeries, while improving symptom-relief, patient satisfaction, and the potential associated financial burdens.

The research study will evaluate the effects of novel stimulation patterns on tremor, bradykinesia, rigidity and gait in Parkinson's disease and essential tremor patients.

Study Design

Study Type:
Observational
Actual Enrollment :
30 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Battery-preserving Stimulation Patterns to Improve Symptoms in Parkinson's Disease and Essential Tremor
Study Start Date :
May 1, 2014
Actual Primary Completion Date :
Apr 1, 2016
Actual Study Completion Date :
Sep 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Biphasic DBS stimulations

Subjects in this group will have Biphasic DBS stimulation setting performed, Unified Parkinson's Disease Rating Scale (UPDRS), Tremor Rating Scale (TRS), kinesia accelerometer assessment, Trigno wireless system (EMG) assessment and GaitRite walking assessment performed.

Device: Biphasic DBS stimulation
The following protocol will be followed for each subject. In between, baseline and novel stimulation settings there will be a 30-minute washout period with DBS in the off state. Current best/optimized DBS setting (considered "baseline") DBS off for 30 minutes as a washout period Biphasic pulse stimulation mode (assessment at 0.5hr) Biphasic pulse stimulation mode (assessment at 1hr) Biphasic pulse stimulation mode (assessment at 2hr) Biphasic pulse stimulation mode (assessment at 3hr)

Other: Unified Parkinson's Disease Rating Scale
UPDRS is used by neurologists to rate the motor impairment of people with Parkinson's Disease.
Other Names:
  • UPDRS
  • Other: Tremor Rating Scale
    TRS is used by neurologists to rate the severity of a tremor.
    Other Names:
  • TRS
  • Device: Kinesia accelerometer
    The kinesia accelerometer is used to analyze the tremor and slowness (bradykinesia) of the participants.

    Device: Trigno wireless system
    The Trigno system measure muscle contractions.

    Other: GaitRite walking assessment.
    GaitRite records a patients gait pattern.

    Outcome Measures

    Primary Outcome Measures

    1. Evaluate the efficacy of novel stimulation patterns by the Unified Parkinson's Disease Rating Scale [Baseline to Day 1]

      The Unified Parkinson's Disease Rating Scale (UPDRS) is used by neurologists to rate the motor impairment of people with Parkinson's Disease. The rater obtains the score by observation and questioning the participant. Higher scores represent greater impairment and scores range from 0-108. The subject will be videotaped and two raters blinded to conditions will score the UPDRS.

    2. Evaluate the efficacy of novel stimulation patterns by the Tremor Rating Scale [Baseline to Day 1]

      Tremor Rating Scale (TRS), consists of 11 items that evaluate tremor in the head, arms, and legs. The rater assigns a score of 0 to 4 for each item, in ascending order of severity. The subjet will be videotaped and two raters blinded to conditions will score the TRS.

    3. Kinesia accelerometer to measure motor dysfunction [Baseline to Day 1]

      The Kinesia system includes a unit worn by the subject and software that is used to collect, manage, and analyze data. The system measures three-dimensional motion using three orthogonal accelerometers and three orthogonal gyroscopes located in the sensor module.The digital data is received by the Receiver connected to a computer and processed by the Kinesia software package.

    4. Trigno wireless system to measure motor dysfunction [Baseline to Day 1]

      This system has sensors with a multi-function design and therefore along with recording of surface EMG signal, it allows Triaxial Accelerometry. This wireless EMG machine will measure muscle contractions.

    5. GaitRite walking assessment. [Baseline to Day 1]

      The GaitRite is an automated floor that when the subjects walk on the floor it records the gait pattern.

    Secondary Outcome Measures

    1. Battery Consumption compared between pre and post settings [Baseline to Day 1]

      Battery consumption will be calculated and compared between the new settings and subjects' baseline settings. The Medtronic battery estimator helpline will be used to calculate battery life, as well as the University of Florida calculator.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Diagnosis of Parkinson's disease or Essential Tremor by strict criteria

    • Deep brain stimulation (DBS) already implanted

    • Optimized Deep brain stimulation (DBS) settings (or at least 4 months of DBS programming)

    Exclusion Criteria:
    • Other neurological diagnoses (co-existent Alzheimer's or ALS)

    • No Deep brain stimulation (DBS)

    • less than 4 Deep brain stimulation (DBS) programming

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Center for Movement Disorders and Neurorestoration Gainesville Florida United States 32607

    Sponsors and Collaborators

    • University of Florida

    Investigators

    • Principal Investigator: Micheal Okun, M.D., University of Florida

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Florida
    ClinicalTrials.gov Identifier:
    NCT02569021
    Other Study ID Numbers:
    • IRB201501030
    First Posted:
    Oct 6, 2015
    Last Update Posted:
    Oct 24, 2016
    Last Verified:
    Oct 1, 2016
    Keywords provided by University of Florida
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 24, 2016