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N/A N=831 Randomized Screening

Community Collaboration to Combat COVID-19 (C-FORWARD)

Coronavirus Infection

Enrolled (actual)
831
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Uptake of SARS-CoV-2 Testing as Assessed by Proportion of Participants Who Complete Testing — 199; 205; 218; 78 Participants — p=0.67

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Fixed site standard of care testing (Behavioral); Community-based, mobile van testing (Behavioral); Self-collected, home-based testing (Behavioral)
Age
Pediatric, Adult, Older Adult · 5+ yrs
Sex
All
Sponsor
Johns Hopkins University
Primary completion
Jun 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Uptake of SARS-CoV-2 Testing as Assessed by Proportion of Participants Who Complete Testing
199; 205; 218; 78; 68; 63 0.67
SECONDARY
Time to Completion of SARS-CoV-2 Testing
7; 6; 7 0.14
SECONDARY
Time From SARS CoV-2 Testing to Receipt of Results
3; 3; 3 0.56

Summary

This is randomized trial where households will be randomized to identify the optimal SARS-CoV-2 (COVID-19) testing modality in a population-representative sample of households in Baltimore City, Maryland. 1,386 households in Baltimore City will be randomized 1:1:1 to one of three testing modalities: 1) fixed-site standard of care testing; 2) community-based mobile van testing; or 3) self-collected home, based testing.

Eligibility Criteria

Inclusion Criteria for households

  • Selected address within Baltimore City
  • At least one member of the household >18 years of age who speaks English and/or Spanish
  • At least one member of the household provides informed consent
  • At least one member of the household psychologically fit to complete survey

Inclusion Criteria for Individuals

  • Reports primary residence within the sampled household
  • Provides informed consent
  • For children (12 years of age or older), with child assent.

Exclusion Criteria for households:

  • Adult member of the household is under the influence of illicit substances, in the opinion of the phone interviewer
  • Residents of nursing homes, half-ways houses or shelters
  • Psychologically unfit to complete the survey
  • Not a selected household address

Exclusion criteria for individuals

  • Person providing informed consent is under the influence of illicit substances
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04673292). 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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