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Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems

M.D. Anderson Cancer Center · NCT06843720

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–65 · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
7100
US sites recruiting
1
Study start
February 17, 2025
Record last updated
June 23, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

To learn about the attitudes toward implementing self-collection among healthcare providers and staff, participants, and other stakeholders; and to inform the development of patient education and provider training materials to aid in the implementation of self-collection in clinical settings.

Being studied: HR-HPV Testing

Conditions: HR-HPV Testing

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

Populations involved in the research are

  • stakeholder advisory board members;
  • patients eligible for cervical cancer screening participating in the cluster randomized stepped-wedge trial;
  • patients and community members participating in formative research activities;
  • providers, clinic staff, and other health system stakeholders from partnering health systems;
  • Project ECHO Participants (providers, clinic staff, and other health system stakeholders from partner and non-partner institutions);
  • Other Clinical Networks (providers, clinic staff and other health system stakeholders from partner and non-partner institutions)

The eligibility criteria for each are

Patients eligible for cervical cancer screening:

  • Currently a resident in the state of Texas
  • Attend for care at a partner clinic enrolled in the study
  • Women and persons with a cervix
  • Age 25-65
  • Due or past due for cervical cancer screening

Patients and community members participating in formative research activities:

  • Purposively identified as a stakeholder for formative research by research staff

Providers, clinic staff, and other health system stakeholders from partnering health systems:

  • Employed at least part-time by a partnering health system
  • Age 18+

Project ECHO Participants

  • Participate in at least one Project ECHO session
  • Age 18+

Other Clinical Networks

  • Participate in at least one clinical network session
  • Age 18+

Exclusion Criteria

Patients eligible for cervical cancer screening:

  • Report being currently pregnant
  • History of total hysterectomy
  • History of cervical cancer

Other study populations

  • Unable to communicate in English or Spanish

Vulnerable Populations Participants/samples belonging to vulnerable populations (children, pregnant women, cognitively impaired adults, or prisoners) will be prohibited from participation.

Recruiting US locations

  • MD Anderson Cancer Center

    Houston, TX 77030

    Site contact: Jane R Montealegre, PHD · 713-745-5008 · jrmontealegre@mdanderson.org

Study contacts (from the official record)

  • Jane R Montealegre, PHD · 713- 745-5008 · jrmontealegre@mdanderson.org
All healthy volunteers studies in Texas →
Expanding Access to Cervical Cancer Screening Through Primary… (NCT06843720) | Bored Studies