CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Symptoms entered into the CovidX applicationWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


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Name (Synonyms) Correlation

Correlated MeSH Terms (1)


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D004630 Emergencies NIH 0.18

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 Feasibility of Self-monitoring and Patient Decision Support for Suspected COVID-19 Patients After Emergency Department Discharge

This feasibility study is being conducted to understand how discharged emergency department patients who were tested for the SARS-CoV-2 virus (COVID-19) engage with a symptom-tracking web application. Study participants that are enrolled in the study will be asked to enter daily information about their health into the CovidX web application (app.). In addition, patients will answer questions regarding anxiety levels, use a pulse oximeter to record information (if you own one or are given one). The investigators predict that participants will be able to engage with the CovidX web application over several days to weeks for the purposes of symptom tracking, and may have decreased anxiety over the study period.

NCT04462783 COVID Covid-19 SARS-CoV 2 Other: Symptoms entered into the CovidX application
MeSH:Emergencies

Primary Outcomes

Measure: Change in the percent of participants using the CovidX web application (app) on 50% or greater of days

Time: baseline, up to 30 days

Measure: Average compliance rate with daily symptom tracking by day 30

Time: Day 30

Description: The proportion of patients approached for the study who enroll

Measure: Recruitment rate

Time: through study completion an average of 1 year

Secondary Outcomes

Description: The PROMIS Emotional Distress-Anxiety-Short Form 4a is a 4-item scale that assesses fear, anxiety, worry, and uneasiness. It uses a 5-point Likert scale (1 = never to 5 = always). Raw scores range from 4-20 with lower scores representing less endorsement of anxiety.

Measure: Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety short form 4a

Time: completed at baseline (enrollment), up to 30 days

Description: This is a 5- item questionnaire that assess anxiety related to the Coronavirus. Participants select from (0 = not at all to 4 = nearly every day over the last 2 weeks). The higher the total number the more anxiety.

Measure: Change in Coronavirus Anxiety Scale

Time: completed at baseline (enrollment), up to 30 days

Description: The questionnaire is a series of 8 questions answered on a 1-7 Likert scale, with lower numbers indicating better usability. There are also 2 open-ended questions about why participants did or didn't like the application and other feedback is collected.

Measure: CovidX web application usability and utility measured adapted by mHealth App Usability Questionnaire

Time: 30 days

Description: This will be measured by the compliance rates

Measure: Differences in CovidX web application engagement between patients who do and do not receive a pulse oximeter

Time: 30 days


No related HPO nodes (Using clinical trials)