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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

RecruitingHealthy volunteers welcome

Who can join

Ages 18 to 65 · Women · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

Populations involved in the research are:

1. stakeholder advisory board members;
2. patients eligible for cervical cancer screening participating in the cluster randomized stepped-wedge trial;
3. patients and community members participating in formative research activities;
4. providers, clinic staff, and other health system stakeholders from partnering health systems;
5. Project ECHO Participants (providers, clinic staff, and other health system stakeholders from partner and non-partner institutions);
6. 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.

About the study

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.

What is being tested

Sponsor: M.D. Anderson Cancer Center · Participants: 7,100 · Started: Feb 17, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06843720

Locations in the U.S.

TexasMD Anderson Cancer Center, Houston

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.