Trials / Completed
CompletedNCT03898167
Prospective Evaluation of Self-Testing to Increase Screening
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
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 2,474 (actual)
- Sponsor
- Baylor College of Medicine · Academic / Other
- Sex
- Female
- Age
- 30 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
Regularly attending for Pap test cervical cancer screening in a clinic is often unfeasible and/or unacceptable to many women. This study 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.
Detailed description
Regularly attending for Pap test cervical cancer screening in a clinic is often unfeasible and/or unacceptable to many women. Using mailed self-sampling kits to test for high-risk human papillomavirus (HPV), the virus that causes cervical cancer, may overcome multiple barriers to clinic-based screening. This study is a randomized controlled trial to compare the effectiveness of three outreach interventions to increase primary screening participation and clinical follow-up among underscreened women a in a safety net health system. The three strategies that will be evaluated are: 1) telephone recall; 2) telephone recall with mailed self-sample HPV testing kits; and 3) telephone recall with mailed self-sample HPV testing kits and patient navigation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2020-02-13
- Primary completion
- 2024-03-01
- Completion
- 2025-03-31
- First posted
- 2019-04-01
- Last updated
- 2025-09-04
- Results posted
- 2025-09-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT03898167. Inclusion in this directory is not an endorsement.