Меню
Идёт набор NCT05435300

Does tDCS Change Synaptic Density in the Brains of Patients With Schizophrenia

— Наблюдательное Schizophrenia Schizoaffective

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: PET Scan.
Кому может быть актуально
Состояния в реестре: Schizophrenia, Schizoaffective. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Канада
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Не всё понятно в терминах? Прочитайте наш гид для пациентов →

Обзор

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).

Подробное описание

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.

Вмешательства

  • Другое PET Scan
    Participants will undergo two PET scans throughout the study.

Первичные конечные точки

  • Synaptic density changes [Срок оценки: 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)]

Критерии участия

Критерии включения

Enrolment in the tDCS-adherence parent study (REB# 103-2018). The parent study inclusion criteria are:

  • Male or female participants of any race or ethnicity
  • Inpatients or outpatients ≥18 years of age
  • DSM-V diagnosis of schizophrenia or schizoaffective disorder
  • Capable of consenting to participate in the research study
  • On a stable dose of oral antipsychotic drug and other concomitant medications for at least 2 months, and unlikely to undergo changes in dose during the study.

Критерии исключения

The exclusion criteria for this study will be the same as the parent study (REB 103-2018). The parent study exclusion criteria are:

  • Unwilling or incapable to consent to the study based on the MacArthur Test of Competence
  • Unstable medical or any concomitant major medical or neurological illness, including a history of seizures
  • Acute suicidal or homicidal ideation
  • Formal thought disorder rating ≥3 on the Positive and Negative Syndrome Scale (PANSS) P2 conceptual disorganization item
  • DSM-V substance dependence (except caffeine, nicotine, and cannabis/marijuana) within 1 month of entering the study
  • Positive urine drug screen except for cannabis/marijuana at the screening visit
  • Metal implants or pacemaker precluding an MRI scan or other contraindications to MRI (e.g., claustrophobia)
  • Pregnancy
  • Score <32 on the Wide Range Achievement Test-III

Additional exclusion criteria for this companion study are:

  • Unwilling or incapable to consent to the study based on the MacArthur Test of Competence
  • Exposure to long-acting injectable antipsychotics in the last 6 months
  • Exceeding allowed annual radiation exposure levels (20 mSv), as outlined by our PET Centre guidelines
  • Receiving treatment with medications such as levetiracetam that blocks SV2a binding
  • Disorders of coagulation or taking anticoagulant medication
  • Having completed multiple PET scans in the past, such that participation in this study would cause participant to exceed lifetime limit (8 PET scans)

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Только случаи

Центры проведения

Канада · 1 центр
  • Centre for Addiction and Mental Health — Toronto

Идентификаторы

NCT: NCT05435300 · 118/2020

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗