DBS Virtual Learning Experience
The Value of Virtual Education on Deep Brain Stimulation for Surgical Candidates
1 other identifier
interventional
60
1 country
1
Brief Summary
The success of Deep Brain Stimulation (DBS) is more correlated to fulfillment of patients' expectations, than merely improvement of motor status1. Therefore, it is of utmost importance to inform the DBS candidates as good as possible to set realistic expectations. Currently, the patient - most of the time accompanied by a family member - is informed about the surgery and its benefits and risks during the outpatient consultation of the neurologist, and later on during the consultation of the neurosurgeon. Written information is provided in the form of a booklet that the patients take home. Due to the large amount of information, not all of it can be captured by the patient. Therefore, we would like to investigate whether an additional online immersive educational session on DBS would better educate the patient. The online session is a 1-hour video call with a small group of DBS candidates and their caregivers, lead by DBS experts, where testimonials of other patients are shown, together with multiple infographics. Two weeks later their will be a second online session summarizing the information and providing the opportunity for Q\&A.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable parkinson-disease
Started Sep 2023
Typical duration for not_applicable parkinson-disease
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2023
CompletedFirst Submitted
Initial submission to the registry
May 24, 2024
CompletedFirst Posted
Study publicly available on registry
May 31, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2026
CompletedSeptember 22, 2025
September 1, 2025
2.3 years
May 24, 2024
September 16, 2025
Conditions
Outcome Measures
Primary Outcomes (5)
The Parkinson's Disease Questionnaire (PDQ-39)
This questionnaire assesses how often people with Parkinson's experience difficulties. across 8 dimensions of daily living. The total score for each dimension ranges from 0 (never have difficulty) to 100 (always have difficulty). Lower scores indicate better quality of life.
Baseline, 3 months post op
MDS-UPDRS (Movement Disorders Society Unified Parkinson's Disease Rating Scale)
Is composed of 4 parts4. Part 1 in on the non-motor aspects of experiences of daily living, with the first half begin rated by the health care professional, based on input from the patient and the caregiver; and the second half a patient questionnaire. Part 2 is on the motor aspects of experiences of daily living, which is a questionnaire filled out by the patient and the caregiver. In the 3rd part the motor condition of the patient evaluated by the physician or nurse practitioner, in meds-ON and DBS-ON condition. The fourth and final part evaluates the motor complications and is rated by the health care professional, based on input from the patient and the caregiver. The total score on the MDS-UPDRS ranges from 0 to 260. The score indicates: 0: No disability 260: Total disability.
Baseline, 3 months post op
Parkinson Anxiety Scale (PAS)
is a 12-item observer or patient-rated scale with three subscales, for persistent and episodic anxiety, and avoidance behaviour. The total score on the PAS can range from 0 to 48. Higher scores indicate greater experiences of anxiety
Baseline, 3 months post op
The Beck Depression Inventory (BDI)
Is a 21-items questionnaire that is filled out by the patient to self-rate mood-related statements. The total score can range from 0 to 63. Higher scores indicate greater severity of depressive symptoms.
Baseline, 3 months post op
Structured survey
Assesses the level of knowledge (score range: 0-110), anxiety (score range: 0-100), expectation (score range: 0-100), satisfaction (score range: 0-80).
Baseline, one day before surgery, 3 months post op
Study Arms (2)
Educational Group
EXPERIMENTALPatients will receive two extra virtual educational sessions.
Standard-of-Care
NO INTERVENTIONPatients will not receive any extra educational sessions. Their education will be provided as per standard-of-care by the clinical team.
Interventions
Two online educational sessions will be organized before DBS surgery. These will be scheduled between consultation with the neurologist and the consultation with the neurosurgeon. Each virtual session will last about 1 hour. Patients can login from home, together with their caregivers. The virtual sessions will be held on MS Teams virtual platform. One of the sessions will include a DBS patient where patients will have the opportunity to ask peer-to-peer questions. The session includes testimonials from patient before and after their surgery. The second session (about two weeks later) is a summary presentation, a quiz and time for Q\&A. During one of the sessions (first or second), a DBS patient (who has been implanted) can be invited to participate togive the attendees the opportunity to ask peer-to-peer questions. The quiz contains questions to assess the patients' knowledge of DBS.
Eligibility Criteria
You may qualify if:
- Patients of any age over 18 who are capable of understanding and granting informed consent.
- Consecutive enrollment of Parkinson's disease patients, eligible for DBS surgery who will be operated in Toronto Western Hospital.
- Targets of surgery (STN or GPi) equally in each study arm.
- Patients must be able to follow the assessment procedure.
You may not qualify if:
- \. people with limited digital skills (to the discretion of the PI).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Movement Disorders Centre - Toronto Western Hospital
Toronto, Ontario, M5T 2S8, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Department of Medicine, Division of Neurology at University of Toronto, Toronto Western Hospital
Study Record Dates
First Submitted
May 24, 2024
First Posted
May 31, 2024
Study Start
September 1, 2023
Primary Completion
December 30, 2025
Study Completion
February 1, 2026
Last Updated
September 22, 2025
Record last verified: 2025-09