Centre for Addiction and Mental Health
Toronto, Ontario, M5T 1R8, Canada
Location status: Recruiting
Location contact
Ariel Graff, MD, PhD
CONTACT
416-535-8501 ext. 34834
Philip Gerretsen, MD, PhD
CONTACT
416-535-8501 ext. 39426
NCT Number: NCT05435300
This study will examine changes in synaptic density with transcranial direct current stimulation (tDCS) in the brains of patients with schizophrenia. Synaptic density levels will be measured using a novel positron emission tomography (PET) radiotracer [18F]SDM-8, which is currently the best-in-class method to quantify synaptic density in humans. This will be a companion study to a parent study by our group examining the effects of tDCS on treatment adherence in schizophrenia (REB #103-2018).
Interested in participating?
Request Info18 year and older
All sexes
Observational
Toronto, Ontario, M5T 1R8, Canada
Location status: Recruiting
Ariel Graff, MD, PhD
CONTACT
416-535-8501 ext. 34834
Philip Gerretsen, MD, PhD
CONTACT
416-535-8501 ext. 39426
The aim of our study is to examine if tDCS induces synaptic density changes in patients with schizophrenia using [18F]SDM-8. Our study will help elucidate the mechanism through which tDCS affects the brain.
PET scans will be offered to participants that meet the inclusion and exclusion criteria at the initial screening visit. Participants will be scanned with the novel PET tracer [18F]SDM-8 to quantify synaptic density levels. PET scans will be timed to coincide to the two time-points, before and after 2-weeks of tDCS treatment that is completed under the parent study protocol (REB #103-2018). Clinical assessments will be done at the same time.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Enrolment in the tDCS-adherence parent study (REB# 103-2018). The parent study inclusion criteria are:
Exclusion criteria
The exclusion criteria for this study will be the same as the parent study (REB 103-2018). The parent study exclusion criteria are:
Additional exclusion criteria for this companion study are:
Participants will undergo two PET scans throughout the study.
Time frame: PET scans will be timed to coincide to the two time-points, before and after 2-weeks of tDCS treatment that is completed under the parent study protocol (REB #103-2018)
The primary outcome measure is the [18F]SDM-8 standard uptake value (SUV) and distribution volume ratio (DVR) in cortical and subcortical gray matter regions, measured by PET Scans
Contact information is provided by the study sponsor or research team.
Ariel Graff, MD, PhD
CONTACT
416-535-8501 ext. 34834
Philip Gerretsen, MD, PhD
CONTACT
416-535-8501 ext. 39426
Centre for Addiction and Mental Health
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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