Parkinson Disease
Conditions
Keywords
deep brain stimulation
Brief summary
Exploring directional lead
Detailed description
This is a single-centre, double-blinded cross-over study comparing the standard electrode configuration (ring-mode) vs. directional electrode configuration for steered stimulation of deep brain stimulation (DBS) patients. The study will follow 2 phases. Phase 1: Visit 1 Screening/Baseline (T0): As per current standard care for patients undergoing subthalamic deep brain stimulation (STN-DBS), participants will be screened 3-6 months before the DBS STN implant surgery (T0) according to the inclusion/exclusion criteria. Visits for standard practiced care for programing of DBS Between 1 to 3 months after the surgery, programing of the DBS system for the 20 patients will be done in an open label fashion in order to find the contact able to reduce the motor symptoms without the side effects. This will be done according to the standard of practice currently adopted at Toronto Western Hospital. Phase 2: Visit 1 Randomization: 4 months +/- 4weeks after the surgery, patients will be randomized to two type of stimulation: 1. Standard : The percentage of current allocated to the central split contacts will be evenly distributed in order to perfectly mimic a standard ring contact. All possible types of frequencies and pulse widths will be used. The same amount of current for each of the active contacts will be used. 2. Directional: contacts 1-8 will be used in any possible configuration and using different amount of current for each of the active one as well as different frequencies. In conclusion, all the capabilities of the DBS system will be used. Possible adjustments to stimulation parameters (e.g. pulse width, amplitude threshold) will be performed to achieve an optimal therapeutic window for each patient. Visit 2 Follow up visit at 6 months +/- 4 weeks of the surgery for neurological examination if required. Visit 3 (T1): Cross over : 7 months +/- 4 weeks after the surgery patients will be switched to the other type of stimulation . Raters and patients will be blinded to the group allocation. Visit 4: Follow up visit at 9 months +/- 4 weeks of the surgery for neurological examination if required. Visit 5 (T2): End of study visit at month 10 +/- 4 weeks after the surgery. There might be unscheduled visits in case of unexpected clinical conditions (i.e. occurrence of side effects or worsening of motor conditions). Participants will be in this study for a maximum of 16 months. Throughout the whole study, participants will visit the clinic without their regular medication as part of standard treatment practice. All the stimulation adjustment will be performed by the same unblinded physician or sub-investigator.
Interventions
DEVICEDeep brain stimulation
Steered stimulation using directional leads
Sponsors
University of Toronto
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Patients with a diagnosis of Parkinson's disease (PD) according to the British Parkinson's Disease Society Brain Bank criteria, who fulfilled the inclusion and
Exclusion criteria
proposed by the core assessment programme for surgical interventional therapies in PD panel 2. Male and female patients with idiopathic PD, who have symptoms responsive to L- dopa medications, but who have significant impairment related to PD that is no longer well controlled with pharmacotherapy (i.e., refractory to optimized medical therapy) 3. Patients considered as subthalamic nucleus deep brain stimulation (STN-DBS) candidates as per current standard of care. These patients will subsequently undergo STN-DBS surgery and maintain stimulation therapy. 4. Patients aged 18 to 80 years. 5. Quality of life and social functioning influenced by levodopa-responsive symptoms 6) No major comorbidities
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number/incidence of adverse events | Throughout the study, averaging 6 months | Number/incidence of adverse events |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Patients Global Impression of Change (PGIC) | After 3 months of each intervention | The PGIC evaluates all aspects of patients' health and assesses if there has been an improvement or decline in clinical status relative to baseline. This is a seven point scale, lower values indicating worsening and higher values, improvement. |
| Change in articulation rate of speech using a Phonetics Software | After 3 months of each intervention | Sample speeches will be recorded and digitalized at 44,000Hz using a microphone and analyzed with a Phonetics software. Articulation rate is calculated as the number of syllables produced/total time without pauses. |
| Change in dysfluency of speech using a Phonetics Software | After 3 months of each intervention | Sample speeches will be recorded and digitalized at 44,000Hz using a microphone and analyzed ina Phonetics software. Dysfluency is calculated as percentage of dysfluent words/total number of words. Dysfluent words are defined as part-words, word or phrase repetitions, revisions, hesitations or fillers. |
| Change in intelligibility of speech using a Phonetics Software | After 3 months of each intervention | Sample speeches will be recorded and digitalized at 44,000Hz using a microphone and analyzed in a Phonetics software. Intelligibility is a subjective measure of speech quality, and will be measured by a single rater trained in speech-language pathology. |
| Change in the Movement Disorders sponsored Unified Parkinson's disease Rating Scale (MDS-UPDRS), a measure of various motor and non-motor symptoms used to assess the clinical course of Parkinson's longitudinally. | After 3 months of each intervention | The MDS-UPDRS scores range from 0 to 272, with higher scores meaning more severe disease |
| Change in the presence and severity of depressive symptoms using the Beck Depression Inventory (BDI) | After 3 months of each intervention | The BDI is a 21-question multiple-choice self-report inventory for measuring the severity of depression. Scores range from 0 to 63, with higher scores meaning worse depression. |
| Walking speed measured with the Zeno Walkway | After 3 months of each intervention | The Zeno Walkway is a 20 feet walking mat containing 16-pressure sensing pads and circuitry that allows for measurement of various gait and balance variables during straight walking. Patients will be asked to walk on the mat at a self selected pace. Walking speed will be measured. |
| Change from baseline in a measure of health related quality of life and non-motor symptoms of Parkinson's disease using the Parkinson's disease Questionnaire (PDQ-39) | After 3 months of each intervention | The PDQ-39 assesses individuals experiences across 8 dimensions of daily living. Each dimension is scored from 0 to 100. Lower scores mean better quality of life. |
| Double support time measured with the Zeno Walkway | After 3 months of each intervention | The Zeno Walkway is a 20 feet walking mat containing 16-pressure sensing pads and circuitry that allows for measurement of various gait and balance variables during straight walking. Patients will be asked to walk on the mat at a self selected pace. Mean and coefficients of variation (standard deviation divided by the mean x 100) of double support time will be measured. The double support time is the the time during gait where both feet are in contact to the ground |
| Cadence measured with the Zeno Walkway | After 3 months of each intervention | The Zeno Walkway is a 20 feet walking mat containing 16-pressure sensing pads and circuitry that allows for measurement of various gait and balance variables during straight walking. Patients will be asked to walk on the mat at a self selected pace. Mean and coefficients of variation (standard deviation divided by the mean x 100) of cadence will be measured. Cadence is the number of steps per minute of walking. |
| Percentage of ON time without troublesome dyskinesias during waking hours | After 3 months of each intervention | ON time without dyskinesias is defined as the period of time is which patients have good mobility, associated with a good response to treatments and without troublesome involuntary movements (dyskinesias). This will be measured as percentage of ON time during the waking hours of the day, Patients will complete 24-hours motor diaries during 3 consecutive days, in which they are asked to rate their motor functions every 30 minutes. |
| Number of falls or near-falls | Collected after 3 months of each intervention, but assessing all intervention period, averaging 6 months | Participants will be asked to keep track of all falls and near-falls (an event in which a person feels a fall is imminent but avoids it by compensatory action, such as grabbing a nearby object or controlling the fall) on a written diary throughout the intervention period. |
| Change in levodopa equivalent daily dose (LEDD) | After 3 months of each intervention | LEDD is calculated using a conversion formula to transform all medications used for treatment of Parkinson's disease to an equivalent dose of levodopa |
| Measure of resting-state local field potentials and functional connectivity of the brain using magnetoencephalography (MEG) | After 3 months of each intervention | MEG will be used to measure the average absolute power and the power spectrum density of neuronal activity of the brain, both measures will be used to assess the effect of deep brain stimulation on the functional activity and oscillatory synchronization of various movement-related areas of the brain. |
| Step length measured with the Zeno Walkway | After 3 months of each intervention | The Zeno Walkway is a 20 feet walking mat containing 16-pressure sensing pads and circuitry that allows for measurement of various gait and balance variables during straight walking. Patients will be asked to walk on the mat at a self selected pace. Mean and coefficients of variation (standard deviation divided by the mean x 100) of step length will be measured. |
Countries
Canada
Outcome results
None listed