The Feasibility of Implementing Syphilis Point-of-care Testing Into a Prenatal Clinic for People Facing Barriers to Care

ConditionSyphilis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age13-49
SponsorMcMaster University

About this trial

The goal of this clinical trial is to learn if a finger-prick blood test for rapid diagnosis of syphilis infection can be implemented in a low-barrier prenatal clinic for people at risk of syphilis in pregnancy. The test gives results in 5 minutes and also tests for HIV.

The main questions the study aims to answer are:

* How often do pregnant people at risk of syphilis agree to the rapid test? * How well do healthcare providers perform the rapid test? * Does the rapid test speed up diagnosis and treatment of syphilis in pregnant people and their sexual partners?

Participants will:

* Give feedback about why they did or did not want to take the rapid test, and what their experience was taking the test; and * Share information about their health, pregnancy, and syphilis treatment (if applicable).

Eligibility criteria

Qualifiers

Pregnant people

Substance use or accessed addiction services in the past 1 year

Unstable housing in the past 1 year

Multiple sexual partners in the past 1 year

Disqualifiers

Previous syphilis diagnosis

Not competent to consent to study participation

Sexual partners

Sexual partners of pregnant clients who are newly diagnosed with syphilis

Trial design

Treatments tested in this trial

  • Rapid Syphilis/HIV point-of-care test

Treatment groups

77 Participants
are divided into 1 treatment group

Sponsors and collaborators

McMaster University

Lead sponsor

Canadian Institutes of Health Research (CIHR)

Collaborator