MST for Parkinson's Disease

Last updated: December 18, 2024
Sponsor: University of British Columbia
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Depression

Depression (Major/severe)

Tardive Dyskinesia

Treatment

Magnetic Seizure Theapy (MagPro XP MST)

Clinical Study ID

NCT04784494
H19-01049
  • Ages > 50
  • All Genders

Study Summary

This trial aims to test the feasibility of Magnetic Seizure Therapy (MST) for Depression in patients diagnosed with Parkinson's Disease.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Are outpatient or inpatient persons capable of providing informed consent;

  2. ≥50 years old;

  3. Confirmed diagnosis of Parkinson's disease based on UK Brain Bank criteria;

  4. Hoehn and Yahr stage between 1-4;

  5. MINI International Neuropsychiatric Interview diagnosis, Version 6 (MINI-6.0.)diagnosis of a current major depressive episode;

  6. IDS score of ≥22 (moderate/severe depression);

  7. Are on stable doses of psychotropic medication;

  8. Are considered to be appropriate to receive convulsive therapy as assessed by anattending psychiatrist and a consultant anaesthesiologist;

  9. Patient may or may not be on antidepressant medication, but If on antidepressantmedication, they should be agreeable to keep their current antidepressant treatmentconstant during the intervention;

  10. are able to adhere to the intervention schedule;

  11. meet the MST safety criteria;

Exclusion

Exclusion Criteria:

  1. Current diagnosis of major neurocognitive disorder other than PD (eg. MultipleSystem Atrophy, Lewy Body Dementia) or dementia (Montreal Cognitive Assessment (MoCA) <21)

  2. Current active psychosis;

  3. Have any of the cardiovascular risk factors listed on the Revised Cardiac Risk IndexScore

  4. Unstable medical conditions that, in the opinion of the Principal Investigator,carries significant risk of exacerbation by either of the study interventions;

  5. Psychotropic medication initiation <4 weeks prior to enrolment (two classes,antiparkinsonsian and antidepressant compounds);

  6. Have an intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlearimplants, or electrodes) or any other metal object within or near the head,excluding the mouth, that cannot be safely removed;

  7. Require a benzodiazepine dose > 2mg/day of lorazepam or equivalent dose or are onany anticonvulsant due to the potential of these medications to limit the efficacyof MST;

  8. Are unable to communicate in English fluently enough to complete theneuropsychological tests;

  9. Have a non-correctable clinically significant sensory impairment (i.e., cannot hearor see well enough to complete the neuropsychological tests).

  10. Have a non-correctable clinically significant sensory impairment (i.e., cannot hearor see well enough to complete the neuropsychological tests).

Study Design

Total Participants: 20
Treatment Group(s): 1
Primary Treatment: Magnetic Seizure Theapy (MagPro XP MST)
Phase:
Study Start date:
September 20, 2021
Estimated Completion Date:
February 28, 2025

Study Description

This is a phase II, single-arm open-label feasibility trial testing the feasibility of MST for dPD. The trial will occur over 18 months at one academic center in Canada (UBC). The enrollment goal is 20 patients with Parkinson's disease and comorbid moderate/severe depression. Research subjects will provide informed consent before enrollment and participation in any research procedures.The study design follows international CONSORT guidelines for the reporting of results in feasibility trials.

Treatment will be administered two days per week (Tuesday/Thursday). This frequency has been chosen as research indicates that depression outcomes at the end of a course of ECT are similar between twice and thrice a week session, but twice a week sessions are associated with fewer cognitive side effects. Depression symptoms will be assessed with the Inventory for Depressive Symptoms. Response and remission will follow standard definition of decrease ≥50% (response) and IDS < 10 (remission). Patients will receive a maximum of 16 treatments. This maximum treatment number was chosen as the number of ECT treatments for an index course in depression is 12, but available data on MST indicates that MST may require more treatment sessions to achieve remission.

Aim 1. To evaluate the feasibility of using MST to treat dPD in preparation for a future definite superiority trial comparing active MST vs. sham MST for depression in Parkinson's disease.

Hypothesis 1a: Enrollment will be ≥70% of the planned target (i.e. 14 out of 20 participants).

Hypothesis 1b: Retention rate of randomized participants will be ≥70%.

Aim 2. To characterize the side effect profile of MST in dPD, with particular emphasis on cardiovascular and cognitive side effects.

Hypothesis 2a: Drop out rates due to side effects during treatment will be ≤10%

Aim 3: To obtain mean, SD, and 95% confidence intervals of potential outcome variables for the future RCT to estimate the sample size of the future RCT.

Aim 4: To explore the use of EEG as a biomarker of treatment response and correlate of response to MST

Connect with a study center

  • University of British Columbia

    Vancouver, British Columbia V6T2A1
    Canada

    Site Not Available

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