Theta Deep Brain Stimulation for Cognitive Enhancement in Parkinson's Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversity of British Columbia

About this trial

Cognitive impairment is common in Parkinson's disease. A recent study demonstrated 40% of people with PD suffer from mild cognitive impairment and \> 80% of patients develop dementia after a disease duration of 20 years. Cognitive impairment significantly impairs quality of life and has limited treatment options. While the pathophysiology of cognitive symptoms in PD is multifactorial, one contributing factor is dysfunction in subthalamic-cortical loops.

The subthalamic nucleus (STN) receives input from distributed regions of the cortex, forming partially segregated parallel networks with sensorimotor regions, associative (cognitive) cortical regions, and limbic cortical regions. These subthalamic-cortical networks are thought to play a domain general role in inhibitory control, which is a fundamental mechanism underlying flexible behavior across motor, cognitive, and affective domains. Information processing in these subthalamic-cortical networks is expressed through oscillatory activity within distinct frequency bands. For example, communication between the STN and prefrontal regions involved in executive function is thought to occur through coherence in the theta (4-8 Hz) frequency band. As a result of these observations, stimulation of the STN at a theta frequency has been investigated as a method of modulating cognitive processes.

Theta stimulation of the STN has been shown to enhance coherence in subthalamic-cortical networks, facilitating information processing and modulating behavior. For example, a recent study demonstrated that theta stimulation of the STN improved working memory performance in PD subjects, while no effect was seen for other frequency bands. The authors performed a post-hoc analysis and found that the effect may be mediated by connectivity between the stimulated STN region and the right dorsolateral prefrontal cortex (DLPFC). While these studies have demonstrated proof of principle, they are limited by small sample sizes and post-hoc analyses assessing the relationship between stimulation location and outcomes. Further research is needed to directly test the hypothesis that theta stimulation of the STN can improve executive control in PD patients by modulating associative STN circuitry.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Those with STN DBS devices

Those with pre- and post-operative imaging

Those that are at least 3 months post-operative

Disqualifiers

Those unable to complete the cognitive task (due to language barriers or dementia)

Those with significant DBS complications

Trial design

Design model

Crossover

Treatments tested in this trial

  • DBS On

    Device

    The DBS device will be turned on while the patient undergoes the working memory task.

  • DBS Off

    Device

    The DBS device will be turned off while the patient undergoes the working memory task.

Treatment groups

27 Participants
are divided into 4 treatment groups
Group A: Stimulation offSham comparator 1 intervention
Group B: Theta stimulation of associative STN regionExperimental treatment 1 intervention
Group C: Theta stimulation of STN sensorimotor regionActive comparator 1 intervention
Group D: High frequency stimulation of associative STN regionActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in working memory performance between conditions

Working memory performance will be assessed through a modified Sternberg task. Subjects will undergo the task with and without stimulation. Measures the main effect of stimulation condition, with hypothesis that theta stimulation of associative STN will improve performance compared to no stimulation. Outcome measured through percent of correctly recalled sequences.

Time frame
Immediately after task performance

Secondary outcomes

1

Interaction effect between groups and stimulation condition

A secondary analysis will categorize subjects into two groups: 1) those where differential targeting of the associative and sensorimotor STN networks was achieved and 2) those where differential targeting of these networks was not possible using the imaging-based criteria previously mentioned. The linear mixed-effect model will be repeated with the addition of an interaction term between group and stimulation condition. The hypothesis is that there will be a significant interaction effect between group and stimulation condition. Specifically, the investigators expect to observe an increase in working memory performance during the theta (6 Hz) stimulation of the associative STN network condition, within the subject group where differential targeting of the associative and sensorimotor STN networks was achieved.

Time frame
Immediately after task performance

Other outcomes

1

Correlation between working memory performance and STN connectivity

Connectivity of the stimulated STN region will be calculated with structural (streamline count and strength) and functional (Pearson Correlation) MRI data. The change in working memory performance will be correlated to the connectivity metrics with a linear regression. The hypothesis is that there will be a positive correlation between working memory change and connectivity strength of the STN to associative networks (higher connectivity will be related to higher working memory performance).

Time frame
Immediately after task performance

Sponsors and contacts

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