Personalized Risk-based Follow-up of Cervical Cancer Screening in Practice, RCT

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age21-70
SponsorMassachusetts General Hospital

About this trial

The goal of this PREDICT is to assess a personalize approach to screening and management of cervical cancer testing. The investigators will evaluate patients who are due for a follow up cervical cancer screening in the primary care clinics in the Massachusetts General Brigham system. Patients will be randomized by clinic into three different arms (Arm 1: standard care, Arm 2: visit based reminders, Arm 3: visit based reminders and population health outreach)

Eligibility criteria

Qualifiers

have a cervix and are 21-70 years old

receive care at a participating primary care practice (i.e. PCP team visit within past 3 years)

have had a Pap and/ or HPV test within the past 3.5 years

has a CCSM result that suggest a 5-year risk of developing CIN3+ that warrants surveillance at 1 or 3 years, diagnostic colposcopy, or treatment (i.e., above average risk).

Disqualifiers

were diagnosed with cervical cancer/ CIN3+ prior to the most recent screening Pap or HPV test

have had their cervix removed

are not English or Spanish-speaking.

Trial design

Treatments tested in this trial

  • Visit-based IT reminders to patients and practitioners
  • Population outreach

Treatment groups

7,500 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators