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临床试验/NCT05040659
NCT05040659进行中(未招募)不适用

Longitudinal At Home Smell Testing to Detect Infection by SARS-CoV-2

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2022年11月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,000
试验地点
1
主要终点
Aromha Longitudinal Smell Test

研究概览

简要总结

The purpose of this study is to learn more about how to better track smell recovery in people who have been infected with the SARS-CoV-2 virus (which causes COVID-19). Many people who have been infected by this virus develop changes in their sense of smell (olfaction). We are interested in measuring smell function objectively via smell cards that test odor intensity, identification, and discrimination. Objective and precise olfactory testing that can be performed in the convenience of one's home will help identify people with smell loss after infection by SARS-CoV-2. We will use results from this test to better understand the relationship between SARS-CoV-2 infection and recovery of olfactory function and to learn whether the AROMHA longitudinal smell test is a reliable olfactory function tracking tool to quantify smell loss in the context of COVID infection. These results may inform the design of therapeutic clinical trials to accelerate the recovery of smell function.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •For anosmic patients/healthy controls:
  • •Inclusion criteria
  • •Known anosmia (for anosmic patients only)
  • •Age greater than or equal to 18
  • •Access to phone, tablet or computer connected to the internet.

排除标准

  • •1. Known odor-evoked adverse effects, e.g. asthma.
  • •For asymptomatic participants:
  • •Inclusion criteria
  • •No symptoms of COVID infection at the time of enrollment.
  • •Age greater than or equal to 18
  • •Access to phone, tablet or computer connected to the internet.
  • •Exclusion criteria
  • •1. Known odor-evoked adverse effects, e.g. asthma.
  • •For participants with COVID-19-related smell loss:
  • •Inclusion criteria
  • •Past infection of SARS-CoV-2 virus as validated by a previous PCR or antigen test
  • •Age greater than or equal to 18
  • •Access to phone, tablet or computer connected to the internet.
  • •Exclusion criteria
  • •1. Known odor-evoked adverse effects, e.g. asthma.

研究组 & 干预措施

Anosmic patients

Anosmic patients will be recruited from Dr. Albers Smell Clinic at MGH and through past participation in research with known anosmia and permission to recontact. All consent and testing will occur on a phone/tablet app in the participant's home.

干预措施: AROMHA Longitudinal Smell Test (Device)

Asymptomatic participants / Healthy participants

Asymptomatic participants recruited in a hospital setting (eg. healthcare workers and household members of symptomatic patients who are potentially COVID positive). No symptoms of COVID infection at the time of enrollment. Potential or definite exposure to SARS-CoV-2 virus without symptoms of upper respiratory infection (smell loss, taste loss, fever, myalgia, cough, nasal congestion, runny nose, shortness of breath). All consent and testing will occur on a phone/tablet app in the participant's home.

干预措施: AROMHA Longitudinal Smell Test (Device)

Participants with a confirmed COVID-19 infection or related smell loss

Individuals who tested positive for SARS-CoV2 by an objective PCR or antigen test will be recruited to evaluate smell function weekly over 3 months. All consent and testing will occur on a phone/tablet app in the participant's home.

干预措施: AROMHA Longitudinal Smell Test (Device)

PASC

Known history of CSD (chemosensory dysfunction) associated with a COVID-19 infection characterized in Dr.Lora Bankova's clinical study (MGB) .

干预措施: AROMHA Longitudinal Smell Test (Device)

结局指标

主要结局

Aromha Longitudinal Smell Test

时间窗: 12 weeks

The Aromha Smell Test is a battery of 18 odors across 6 smell cards. The subject smells each of the 3 scents per card to determine smell intensity, identification, and discrimination. Increased number of correct responses indicates better sense of smell. We will evaluate previously diagnosed anosmic patients.

次要结局

  • Brief Smell Identification Test (BSIT)(12 weeks)

研究者

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

Mark W Albers

Frank Wilkens and Family Endowed Scholar/ Asst. Prof. Neurology

Massachusetts General Hospital

研究点 (1)

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