Transcranial Magnetic Stimulation for Psychological Distress in Patients With Advanced Illness

NARecruitingINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

November 2, 2020

Primary Completion Date

January 20, 2025

Study Completion Date

January 20, 2025

Conditions
Depressive SymptomsDepression, AnxietyPsychological DistressTerminal Illness
Interventions
DEVICE

repetitive Transcranial Magnetic Stimulation (rTMS)

"The rTMS intervention will be performed in a dedicated rTMS patient room on the PC unit, where the patient can remain in their bed seated upwards at a 45 degree angle, or seated in a chair.~The stimulation intensity for treatment will be determined by measuring the resting and active motor threshold (rMT and aMT) using single pulse TMS over the motor cortex using standard techniques as in previous trials. Investigators will use left-sided intermittent theta burst stimulation (iTBS). The trained team member will locate the left DLPFC using the BeamF3 technique. For the open-label dose-finding study, this region will be stimulated intermittently at 3 TMS pulses every 200 milliseconds for 2 seconds (i.e. 30 stimulations). This procedure is repeated every 10 seconds for a total duration of 3 minutes during which 600 total pulses are delivered. Participants will receive up to 8 3-minute sessions daily at 45 minute intervals for 5 days (consecutively or in a seven-day window if need be)."

Trial Locations (1)

K1N5C8

RECRUITING

Elisabeth Bruyère Hospital, Ottawa

All Listed Sponsors
collaborator

Lotte & John Hecht Memorial Foundation

OTHER

collaborator

Bruyère Health Research Institute.

OTHER

collaborator

Canadian Cancer Society (CCS)

OTHER

lead

Ottawa Hospital Research Institute

OTHER