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Battery-preserving Stimulation Patterns for Deep Brain Stimulation

Battery-preserving Stimulation Patterns to Improve Symptoms in Parkinson's Disease and Essential Tremor

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02569021
Enrollment
30
Registered
2015-10-06
Start date
2014-05-31
Completion date
2016-09-30
Last updated
2016-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinsons Disease, Essential Tremor

Keywords

Parkinsons Disease, Essential Tremor, DBS, Depp Brain Stimulation

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.

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.

Interventions

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. 1. Current best/optimized DBS setting (considered baseline) 2. DBS off for 30 minutes as a washout period 3. Biphasic pulse stimulation mode (assessment at 0.5hr) 4. Biphasic pulse stimulation mode (assessment at 1hr) 5. Biphasic pulse stimulation mode (assessment at 2hr) 6. Biphasic pulse stimulation mode (assessment at 3hr)

UPDRS is used by neurologists to rate the motor impairment of people with Parkinson's Disease.

OTHERTremor Rating Scale

TRS is used by neurologists to rate the severity of a tremor.

DEVICEKinesia accelerometer

The kinesia accelerometer is used to analyze the tremor and slowness (bradykinesia) of the participants.

DEVICETrigno wireless system

The Trigno system measure muscle contractions.

OTHERGaitRite walking assessment.

GaitRite records a patients gait pattern.

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the efficacy of novel stimulation patterns by the Unified Parkinson's Disease Rating ScaleBaseline to Day 1The 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.
Evaluate the efficacy of novel stimulation patterns by the Tremor Rating ScaleBaseline to Day 1Tremor 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.
Kinesia accelerometer to measure motor dysfunctionBaseline to Day 1The 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.
Trigno wireless system to measure motor dysfunctionBaseline to Day 1This 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.
GaitRite walking assessment.Baseline to Day 1The GaitRite is an automated floor that when the subjects walk on the floor it records the gait pattern.

Secondary

MeasureTime frameDescription
Battery Consumption compared between pre and post settingsBaseline to Day 1Battery 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026