Clinical Trials Directory

Trials / Completed

CompletedNCT05055505

The School SPIT Study - Elementary Schools in Low COVID-19 Incidence Regions

The School SPIT Study (Saliva to Promote Improved Testing): A Prospective Evaluation of a Home Saliva Testing Program Implemented With a Stepped-wedge Cluster Randomized Design in Elementary Schools in Low SARS-CoV-2 Incidence Regions

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
The Hospital for Sick Children · Academic / Other
Sex
All
Age
2 Years
Healthy volunteers
Not accepted

Summary

This study will conduct an evaluation of a program that is being implemented SickKids / Toronto Public health that provides take-home saliva testing kits in schools. Operationally, there is a planned randomization so that all schools have an equitable chance to receive the intervention at various time periods during the planned operational roll-out, which will require a staggered implementation consistent with the stepped-wedge study design. This study will leverage this chance implementation to do a robust evaluation of the public health intervention. Schools that are not being rolled out to week one, will begin in the "control phase" (testing at an assessment center, primary care or acute care facility) and transition to the program "intervention phase" (take home saliva kits available at schools) at a randomly assigned time (wedge) over a 6-week period with all schools receiving the program by the end of the study. The investigators will evaluate the impact of the program on SARS-CoV-2 case identification in schools.

Detailed description

This is a prospective evaluation of a program that is being implemented using a stepped-wedge, cluster randomized design. Eligible elementary public schools Toronto Region in low SARS-CoV-2 incidence regions (quintiles 1,2 or 3) will be randomized. The study will occur over a 7-week period with a minimum of one-week of baseline data (control phase - testing at an assessment center, primary care or acute care center) and then schools will start the program in a stepwise manner (20 crossovers per week) with take-home saliva being available to all 120 schools by the end of the study period. The primary objective of the study is to assess whether the availability of take home saliva kits at schools for symptomatic testing leads to increased diagnosis of SARS-CoV-2 cases in the school.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTTake home saliva kitsSaliva kits will be made available at schools for pick up to support symptomatic testing using PCR for students, staff and family members.

Timeline

Start date
2021-09-14
Primary completion
2021-11-01
Completion
2022-06-30
First posted
2021-09-24
Last updated
2023-05-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05055505. Inclusion in this directory is not an endorsement.