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ACTIVE NOT RECRUITING
NCT06577220
NA

Prospective Evaluation of Self-Testing to Increase Screening (PRESTIS) Asian/Asian American Women Supplement

Sponsor: Baylor College of Medicine

View on ClinicalTrials.gov

Summary

Regularly attending for Pap test cervical cancer screening in a clinic is often unfeasible and/or unacceptable to many women and persons with a cervix. This study is a supplement to increase representation of Asian and Asian American women in a pragmatic clinical trial that evaluates if mailing and testing self-sampled kits for high-risk human papillomavirus (HPV) can cost-effectively increase screening participation among underserved minority women in a safety-net health system.

Official title: A Randomized Controlled Trial of Mailed Self-Sample HPV Testing to Increase Cervical Cancer Screening Participation Among Minority/Underserved Women in an Integrated Safety Net Healthcare System Asian/Asian American Women

Key Details

Gender

FEMALE

Age Range

30 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

111

Start Date

2023-09-28

Completion Date

2026-01-24

Last Updated

2025-10-14

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Telephone Recall

Participants receive a scripted telephone recall from a trained patient navigator.

BEHAVIORAL

Mailed HPV Self-Sampling Kit

Participants receive a mailed kit that allows them to self-collect a cervical sample in their home and return it to a laboratory for human papillomavirus (HPV) testing.

BEHAVIORAL

Patient Navigation

Participant receives telephone call from patient navigator within 3-5 days of receipt of self-collection kit. Patient navigator provides one-on-one education on cervical cancer screening and self-collection of cervical sample.

Locations (1)

Harris Health System

Houston, Texas, United States