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N/A N=792 Randomized Double-blind Health Services Research

COVID-19 Self-Testing Through Rapid Network Distribution

Covid19

Enrolled (actual)
792
Serious AEs
0.0%
Results posted
May 2025
Primary outcome: Primary: Network Contact Test Uptake — 5; 2 Participants — p=0.45

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
COVID-19 self-test (Behavioral); COVID-19 test referral (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Pennsylvania
Primary completion
Nov 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Network Contact Test Uptake
5; 2 0.45
SECONDARY
Network Contact Test Uptake, End of Study
8; 2 0.11
SECONDARY
Number of Contacts Tested at 8 Weeks
23; 13
SECONDARY
Number of Contacts Tested
31; 16
SECONDARY
Number of Participants With at Least One Network Contact Who Tested Positive for COVID-19 at 8 Weeks
3; 0
SECONDARY
Number of Participants With at Least One Network Contact Who Tested Positive for COVID-19, End of Study
3; 0

Summary

COVID-19, the coronavirus disease caused by SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2), has led to a global pandemic and has exacerbated existing health inequities among vulnerable populations. Despite higher rates of COVID-19 in Black and Latinx individuals compared to White individuals, rates of testing in predominately non-White, low-income communities are significantly lower than in high-income areas. Self-testing, where individuals collect their own samples, is now feasible for the detection of SARS-CoV-2. One promising approach to increase test uptake is the secondary distribution of self-testing kits, where an individual distributes tests to contacts in their social network and encourages them to self-test. The central hypothesis of this clinical trial is that the secondary distribution of SARS-CoV-2 self-tests can significantly expand test uptake among underserved populations. To test this hypothesis, the investigators will conduct a 1:1 randomized controlled trial that will assess a self-testing intervention that promotes the secondary distribution of SARS-CoV-2 test kits compared with test referrals, with a focus on reaching underserved populations.

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Has a working telephone number
  • Willing and able to provide informed consent

Exclusion Criteria

  • Younger than 18 years of age
  • Does not have a working telephone number
  • Prior COVID-19 infection in the past 90 days
  • Previously received a COVID-19 test as part of this COVID-19 research study
  • Unable or unwilling to provide informed consent
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04797858). 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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