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Evidence-Based Approach to Empower Asian American Women in Cervical Cancer Screening

NCT04557423 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 797

Last updated 2026-03-24

No results posted yet for this study

Summary

This is a randomized trial to evaluate the effects of a community-based intervention on increasing cervical cancer screening rates in underserved Asian American (Korean, Vietnamese, and Chinese) women. All women will receive an educational program and navigation assistance. Women in the intervention condition will also receive a self-sampling kit for self-collection of a cervical sample for HPV testing. The investigators will evaluate whether the inclusion of a self-sampling kit increases the proportion of Asian American women who participate in cervical cancer screening.

Conditions

  • Uterine Cervical Neoplasms

Interventions

BEHAVIORAL

Community-Based Education

A previously evaluated educational intervention delivered in community settings. Includes culturally- and linguistically-appropriate materials.

BEHAVIORAL

Navigation to Screening

Community health educators provide navigation assistance to access clinic-based cervical cancer screening.

BEHAVIORAL

HPV Self-Sampling

An HPV self-sampling kit will be provided for home-based collection of cervical samples. Samples will be sent for analysis of HPV subtypes.

Sponsors & Collaborators

  • Temple University

    collaborator OTHER

  • Fox Chase Cancer Center

    lead OTHER

Principal Investigators

  • Carolyn Y Fang, PhD · Fox Chase Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-08
Primary Completion
2025-11-30
Completion
2025-11-30

Countries

  • United States

Study Locations

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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 NCT04557423 on ClinicalTrials.gov