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NCT06577220 · ClinicalTrials.gov registry record · NA
Prospective Evaluation of Self-Testing to Increase Screening (PRESTIS) Asian/Asian American Women Supplement
A NA study of Cervical Cancer and Human Papillomavirus Infection, sponsored by Baylor College of Medicine.
- Active
- Registry status
- NA
- Development phase
- 111
- Enrollment target
- 1
- Study location
NCT06577220 is a NA study of Cervical Cancer and Human Papillomavirus Infection that is active but no longer recruiting, run by Baylor College of Medicine. The registered enrollment target is 111 participants, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06577220, a NA study of Cervical Cancer and Human Papillomavirus Infection, is active but no longer recruiting, sponsored by Baylor College of Medicine.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 111 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- BEHAVIORAL Patient Navigation
- BEHAVIORAL Telephone Recall
- BEHAVIORAL Mailed HPV Self-Sampling Kit
Study Locations (1)
Texas
- Harris Health System - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 111 participants |
| Start Date | 2023-09-28 |
| Est. Completion | 2026-01-24 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06577220
The ClinicalTrials.gov registry entry for NCT06577220 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 111 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (81% lower). The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cervical Cancer appearing as the primary indexed condition, and to 3 interventions - of which Patient Navigation is the first listed.
NCT06577220 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06577220 about?
NCT06577220 is a clinical study titled "Prospective Evaluation of Self-Testing to Increase Screening (PRESTIS) Asian/Asian American Women Supplement". 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 ...
What is the current status of trial NCT06577220?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 111 participants. The study started on 2023-09-28. Estimated completion is 2026-01-24.
What conditions does trial NCT06577220 study?
This clinical trial studies the following conditions: Cervical Cancer, Human Papillomavirus Infection.
What interventions are being tested in trial NCT06577220?
The interventions under investigation include: Patient Navigation (BEHAVIORAL), Telephone Recall (BEHAVIORAL), Mailed HPV Self-Sampling Kit (BEHAVIORAL).
Who is sponsoring clinical trial NCT06577220?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06577220 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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