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N/A N=2,778

You and Me COVID Free

COVID-19

Enrolled (actual)
2,778
Serious AEs
Results posted
Jun 2023
Primary outcome: Primary: Main Reason for Testing for COVID-19 — 1632; 493; 238; 343 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Behavioral questionaires (Behavioral)
Age
Pediatric, Adult, Older Adult · 12+ yrs
Sex
All
Sponsor
Duke University
Primary completion
Mar 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Main Reason for Testing for COVID-19
1632; 493; 238; 343; 118; 152
PRIMARY
Number of Positive COVID-19 Test Results
269
PRIMARY
Number of Participants Who Responded That They Have Received a COVID Vaccine
850
SECONDARY
Number of Participants Who Indicated That They Have Access to Necessary Personal Protective Equipment in Work Place
475
SECONDARY
Number of Participants Who Indicated They Have Tested Positive for COVID in Their Lifetime
237
SECONDARY
Number of Participants Who Report Knowing Where to Get COVID-19 Tests in the Community
757
SECONDARY
Number of Participants Who Report COVID Symptoms During Previous Week
627
SECONDARY
Likelihood of Future COVID-19 Vaccination
119; 140; 59; 92; 79
SECONDARY
Reasons for Not Getting a COVID-19 Vaccine
5; 22; 3; 47; 7; 34
SECONDARY
Reasons for Getting a COVID-19 Vaccine
712; 477; 557; 135; 86; 378
SECONDARY
Perspective on Easiest Way to Obtain Free Oral COVID-19 Medications
503; 526; 189; 1225; 209; 87
SECONDARY
Method Used to Test for COVID-19
783; 15; 4; 17; 2

Summary

Observational, study that distributes rapid at-home, self-administered, SARS-CoV-2 antigen testing kits to households within pre-selected communities.

Eligibility Criteria

Inclusion Criteria

  • Self- reported primary residence within the pre-identified communities
  • Age >12 years at enrollment
  • Provision of signed and dated informed consent form

Exclusion Criteria

-None if above are met

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05212883). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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