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Intervention for COVID-19 (VIGIE-COVID Trial)
N/A
Waitlist Available
Led By Jean-Sébastien Paquette
Research Sponsored by Laval University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
VIGIE-COVID Trial Summary
Optimization of the Management of COVID-19 Through Tailored Recommendations to the Citizens
Eligible Conditions
- Citizen Self-Reported Symptoms
- Tailored Recommendations
- COVID-19
VIGIE-COVID Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
improvement in daily fruit consumption
improvement in hand washing behavior
improvement in mask wearing behavior
+3 moreSecondary outcome measures
Platform participation
Platform sustainability long term
Platform sustainability short term
VIGIE-COVID Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
The intervention arm are participants who will receive tailored recommendations about health prevention in a pandemic based on their answers in the survey.
Group II: ControlActive Control1 Intervention
The control group will receive general recommendations about health prevention in a pandemic.
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Who is running the clinical trial?
Réseau de recherche en santé des populations du QuébecUNKNOWN
Laval UniversityLead Sponsor
417 Previous Clinical Trials
171,072 Total Patients Enrolled
4 Trials studying COVID-19
7,885 Patients Enrolled for COVID-19
Réseau-1 QuébecUNKNOWN
1 Previous Clinical Trials
3 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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