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HPV Self-Sampling in Somali Women (Isbaar Project)

NCT05453006 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3367

Last updated 2025-07-10

Study results available
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Summary

This study plans to assess the effect of implementing HPV self-sampling in primary care on uptake of cervical cancer screening in 30-65 year old Somali women who are due for cervical cancer screening.

Conditions

  • Cervical Cancer
  • Papillomavirus Infection
  • Uterine Diseases
  • Uterine Cervical Disease

Interventions

DEVICE

COPAN 552c.80 FLOQSwab

The study will implement HPV self-sampling as an option for cervical cancer screening alongside usual care for Somali women, and evaluate changes pre and post implementation, compared to Fairview non-intervention clinics.

Sponsors & Collaborators

Principal Investigators

  • Rebekah Pratt, PhD · University of Minnesota

  • Rachel Winer, PhD · University of Washington

Study Design

Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-20
Primary Completion
2024-05-19
Completion
2025-05-19

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05453006 on ClinicalTrials.gov