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DBS Virtual Learning Experience

U

University of Toronto

Status

Active, not recruiting

Conditions

Parkinson Disease

Treatments

Other: Educational Sessions

Study type

Interventional

Funder types

Other

Identifiers

NCT06436313
23-5018

Details and patient eligibility

About

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.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients of any age over 18 who are capable of understanding and granting informed consent.
  2. Consecutive enrollment of Parkinson's disease patients, eligible for DBS surgery who will be operated in Toronto Western Hospital.
  3. Targets of surgery (STN or GPi) equally in each study arm.
  4. Patients must be able to follow the assessment procedure.

Exclusion criteria

1. people with limited digital skills (to the discretion of the PI).

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Educational Group
Experimental group
Description:
Patients will receive two extra virtual educational sessions.
Treatment:
Other: Educational Sessions
Standard-of-Care
No Intervention group
Description:
Patients will not receive any extra educational sessions. Their education will be provided as per standard-of-care by the clinical team.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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