Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03551028 · ClinicalTrials.gov registry record · NA

HPV DNA Testing Through Mobile Mammography Unit

A NA study, sponsored by University of Virginia.

Completed
Registry status
NA
Development phase
33
Enrollment target

NCT03551028: Completed NA study, sponsored by University of Virginia.

NCT03551028 is a NA study that has completed, run by University of Virginia. The registered enrollment target is 33 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03551028, a NA study, has completed, sponsored by University of Virginia.

COMPLETED
Registry status
NA
Development phase
33 participants
Enrollment target

Study Summary

Invasive cervical cancer incidence and mortality can be dramatically reduced through early detection and treatment, but many women do not complete screening at recommended intervals. Many low-income women in Virginia remain uninsured and are at significant risk of being medically underserved and failing to complete regular cervical cancer screening. Self-collection of specimens for HPV testing is an innovative approach that may increase access to cervical cancer screening in populations that do not participate in traditional clinic-based screening. Innovative delivery models are needed to reach at-risk populations. This study seeks to explore the acceptability and feasibility of pairing self-collection of HPV samples for DNA testing with mobile mammography in women living in rural Virginia.

Primary Outcome

Assess the cultural acceptability of self-collection for HPV testing among under-screened women in Southwest Virginia specifically who were seeking a mammogram at an episodic clinic. The outcome measure of ACCEPTABILITY was measured through: participants who opted in, or uptake of HPV self collection (yes/no); and intention to follow up upon learning of result.

Interventions

  • DEVICE HPV self collection

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2016-07
Est. Completion 2021-03-31
Phase NA
University of Virginia

449 total trials

What the finished NCT03551028 record still lists

NCT03551028 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which HPV self collection is the first listed.

NCT03551028 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03551028 about?

NCT03551028 is a clinical study titled "HPV DNA Testing Through Mobile Mammography Unit". Invasive cervical cancer incidence and mortality can be dramatically reduced through early detection and treatment, but many women do not complete screening at recommended intervals. Many low-income women in Virginia remain uninsured and are at significant risk of being medically underserved and fai...

What is the current status of trial NCT03551028?

This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2016-07. Estimated completion is 2021-03-31.

What interventions are being tested in trial NCT03551028?

The interventions under investigation include: HPV self collection (DEVICE).

Who is sponsoring clinical trial NCT03551028?

This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03551028's enrollment target sits among peer trials

33 1574th of 2000 higher than 423 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02861898 · 33 participants · Phase 1

    Super-selective Intra-arterial Repeated Infusion of Cetuximab for the Treatment of Newly Diagnosed Glioblastoma

  • NCT04871607 · 33 participants · Phase 2

    Yttrium-90 Labeled Anti-CD25 Monoclonal Antibody Combined With BEAM Chemotherapy Conditioning for the Treatment of Primary Refractory or Relapsed Hodgkin Lymphoma

  • NCT05071937 · 33 participants · Phase 2

    ZEN003694 Combined With Talazoparib in Patients With Recurrent Ovarian Cancer

  • NCT05168618 · 33 participants · Phase 2

    Cabozantinib and Atezolizumab for the Treatment of Metastatic Castration-Resistant Prostate Cancer, The AtezoCab Trial

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT03551028, the US trial registry maintained by the National Library of Medicine. NCT03551028 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.