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NCT04568889

Minnesota COVID-19 Testing Project

Completed NA Last updated 14 October 2022
What this trial tests

NA trial testing A $10 Survey Incentive in Covid19 in 561 participants. Completed in 31 August 2022.

Timeline
28 September 2020
Primary endpoint
31 August 2022
31 August 2022

Quick facts

Lead sponsorHarvard University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposehealth services research
Enrollment561
Start date28 September 2020
Primary completion31 August 2022
Estimated completion31 August 2022
Sites10 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Harvard University

Who can join

18 and older, any sex, with Covid19 or Infectious Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this project is to help the state of Minnesota understand why individuals are not getting tested and potentially identify trusted individuals or organizations that could be used in follow-up work to send messages. Investigators focus on the first two issues of unit and item nonresponse, which is not random across the population and thus could lead to nonresponse bias. To do so, investigators are deploying flyers through 10 Twin City area food shelves and potentially through public housing units with information on how to answer an online questionnaire.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Covid19

Currently open trials in the same condition.

Other Harvard University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04568889.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing