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临床试验/NCT04992195
NCT04992195已完成不适用

Impact of COVID-19 Vaccines on Cerebrovascular Health - a Population-based Study

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 415 人开始时间: 2021年7月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
415
试验地点
1
主要终点
Imaging markers

研究概览

简要总结

Safe and effective severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines may reduce the transmission of and achieve population immunity against the COVID-19 pandemic, which accounted for more than 3.75million deaths worldwide. With World Health Organization's (WHO) effort on ensuring equitable access to COVID-19 vaccines, vaccination rate may increase in the near future.

On the other hand, vaccination hesitancy has emerged as a major hindrance on the global vaccination campaigns in certain areas due to safety concerns, social factors, and public health policies. For instance, a recent survey conducted in Hong Kong showed a low vaccine acceptance rate of 37%. Long-term safety concerns and post-vaccination events relayed by the social media maybe reasons for vaccination hesitancy. Among which, cerebrovascular accidents (CVA) after vaccination were one of the most frequently reported post-vaccination events. These reports ranged from ischemic strokes in elderly patients with multiple cardiovascular co-morbidities, to hemorrhage strokes in otherwise "young-and-fit" adults. While many of these events were investigated by the COVID-19 immunization expert committee, an important premise to address the apprehension of CVA after vaccination is the provision of evidence-based information of the impact of COVID-19 vaccines on brain health.

In this prospective, longitudinal, observational study, we aim to elucidate the relationship between COVID-19 vaccines and cerebrovascular health in healthy citizens in a population-based cohort.

详细描述

We shall recruit all consecutive citizens from a prospective, population-based cohort from the CUHK Brain Health Longitudinal Study free of clinically evident neurological diseases. The CUHK Brain Health Longitudinal Study cohort comprises of an epidemiologically representative sample from all socio-economic classes in the 18 districts of Hong Kong with reference to government census data. All citizens received baseline cognitive assessment and evaluation of metabolic risk factors. Baseline micro- and macro-cerebrovascular abnormalities were evaluated by MRI brain on recruitment.

We shall phone contact the citizens who met the inclusion criteria to enquire their vaccination plan. Citizens who received COVID-19 vaccination (SinoVac or BioNTech) and willing to join the study, our services coordinator, co-investigator or principal investigator will interview and explain the study in details and obtain the participant's consent. After signing the consent, the participant shall undergo a 2nd MRI brain 16 weeks (+/-4 weeks) after the 2nd dose of vaccination. The control group is defined as citizens who have not received any COVID-19 vaccines nor clinically/serologically evident SARS-CoV-2 infection.

We shall collect the following information for the vaccination group:

Demographic data ; Medical co-morbidities ; Laboratory tests at baseline and 16 weeks (+/-4 weeks) after 2nd dose of vaccine and serological testing for IgG antibody. We shall conduct a face-to-face assessment 16 weeks (+/-4 weeks) after the 2nd dose of COVID-vaccine for evaluation of any clinical events, followed by a phone visit every 6 months. Cognitive assessment by MoCA will be performed at baseline, 16 weeks (+/-4 weeks) then every 12 months after the 2nd dose of COVID-19 vaccine.

On the other hand, we shall collect the following information for the control group:

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •All consecutive citizens in the CUHK Brain Health Longitudinal Study cohort who received baseline MRI brain.

排除标准

  • •Citizens with clinically evident stroke or dementia prior to recruitment; or
  • •Citizens who are unable to provide an informed consent; or
  • •Citizen with contraindications to MRI brain, e.g., non-MRI compatible implants, claustrophobia, etc; or
  • •Citizens who had no baseline MRI brain assessment.

研究组 & 干预措施

Vaccination Group

Citizens who received baseline cognitive assessment and evaluation of metabolic risk factors from the CUHK Brain Health Longitudinal Study. Baseline micro- and macro-cerebrovascular abnormalities were evaluated by MRI brain on recruitment and received COVID-19 vaccination (SinoVac or BioNTech).

干预措施: Laboratory tests and Montreal Cognitive Assessment (Diagnostic Test)

Control Group

Citizens who received baseline cognitive assessment and evaluation of metabolic risk factors from the CUHK Brain Health Longitudinal Study. Baseline micro- and macro-cerebrovascular abnormalities were evaluated by MRI brain on recruitment and have not received any COVID-19 vaccines nor clinically/serologically evident SARS-CoV-2 infection.

干预措施: Laboratory tests and Montreal Cognitive Assessment (Diagnostic Test)

结局指标

主要结局

Imaging markers

时间窗: December, 2026

We shall perform cranial MRI examinations in a 3-Tesla scanner (MAGNETOM Prisma; Siemens AG, Munich, Germany). The scanning protocol will employ a standard stroke protocol MRI scan with axial T1-weighted, T2-weighted, FLAIR, susceptibility weighted imaging, diffusion weighted imaging, and time-of-flight magnetic resonance angiography (MRA) sequences.

Imaging analysis

时间窗: December, 2026

Blinded to the time sequence, clinical outcomes and the vaccination status, an experienced neuro-radiologist and an experienced stroke neurologist shall independently evaluate the imaging markers (as stated in endpoint assessment above). Disparity will be resolved by discussion. White matter hyperintensity volume will be gauged by FMRIB's Software Library Brain Intensity Abnormality Classification Algorithm (BIANCA), a fully automated, supervised method for white matter hyperintensities detection. Brain volume will be measured by FMRIB's Software Library voxel-based morphometry analysis.Siemens AG, Munich, Germany). The scanning protocol will employ a standard stroke protocol MRI scan with axial T1-weighted, T2-weighted, FLAIR, susceptibility weighted imaging, diffusion weighted imaging, and time-of-flight magnetic resonance angiography (MRA) sequences.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. IP Yiu Ming Bonaventure

Clinical Lecturer

Chinese University of Hong Kong

研究点 (1)

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