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Clinical Trials/NCT04612660
NCT04612660
Completed
Not Applicable

Human Papillomavirus (HPV) and Cervical Cancer Intervention to Increase Cervical Cancer Screening for Underserved Asian Women

Temple University1 site in 1 country156 target enrollmentSeptember 2014
ConditionsCervical Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervical Cancer
Sponsor
Temple University
Enrollment
156
Locations
1
Primary Endpoint
the change in the rate of cervical cancer screening
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The study was to pilot test the feability of using HPV self-sampling testing to increase cervical cancer screening among under-served Asian women through engaging community-based organizations in the greater Philadelphia and New York City area, addressing a significant global cancer burden, the preventable infection-related cervical cancer.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
July 2015
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • gender: female
  • no current diagnosis of cervical cancer, and
  • have not participated in cervical cancer screening within the past 3 years.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

the change in the rate of cervical cancer screening

Time Frame: baseline, and 6-month follow up

Study Sites (1)

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