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Advancing Cervical Cancer Screening Through the Emergency Department - IIS

Not Applicable
Not yet recruiting
Conditions
Cervical Cancers
HPV
Registration Number
NCT06796738
Lead Sponsor
University of Rochester
Brief Summary

Cervical cancer screening in the Emergency Department

Detailed Description

This will be an effort to deploy HPV self-sampling among Emergency Department patients. Emergency Department patients, in the US and worldwide, are disproportionally under-screened for cervical cancer relative to the general population.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
200
Inclusion Criteria
  • Cisgender women and transgender/non-binary individuals with a cervix,
  • Age 25-65,
  • Able to demonstrate decisional capacity to participate.
Exclusion Criteria
  • Past hysterectomy with cervical removal,
  • Known infection with HIV (as screening recommendations for people with HIV differ from the general population),
  • Non-English speaking.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Uptake of Cervical Cancer Screening150 days post initial intervention

All intervention participants will receive a follow-up call at 150 days to assess uptake of any cervical cancer screening and for completion of the cervical cancer screening process. "Any cervical cancer screening" is defined as uptake of any aspect of the cervical cancer screening process, including self-sampling and/or clinic-based screening. "Completion of the cervical cancer screening process" is defined as completion of recommended clinic-based screening (including colposcopy if HPV 16/18+ or indicated).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Rochester

🇺🇸

Rochester, New York, United States

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