Overview

ASPIRE Pilot: Comparing Self-collected HPV Testing With Visual Inspection With Acetic Acid Screening for Cervical Cancer

Status:
Completed
Trial end date:
2015-12-29
Target enrollment:
0
Participant gender:
Female
Summary
Cervical cancer remains a public health burden, particularly in developing countries such as sub-saharan Africa where the infrastructure for organized screening programs does not exist. As a result, other screening modalities (visual inspection with acetic acid) are the standard of care in such regions. It is now known, persistent infection with an oncogenic Human papillomavirus (HPV) type is a necessary precursor of cervical cancer and evidence is showing HPV testing is a potential, safe and effective alternative to cytology testing (The Pap smear). This study is evaluating the feasibility and acceptance of HPV self-collection vs. VIA in a cohort of women from Kisenyi, Uganda.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of British Columbia
Collaborator:
Makerere University
Treatments:
Acetic Acid
Retinol acetate
Criteria
Inclusion Criteria:

- Aged 30-65yrs

- Living or working in community of Kisenyi, Uganda

- Access to mobile telephone

- Fluent in Luganda, Somali or English

- Competent to provide informed consent

Exclusion Criteria:

- Known to be pregnant at study entry (self-reported)

- Complete hysterectomy

- Prior diagnosis or treatment of cervical dysplasia or cervical cancer