Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems
Recruiting
N/AInterventional Study
HR-HPV Testing
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 65
Sex
Female
Study type
Interventional
Purpose
Screening
Participants needed
7,100 (estimated)
Sponsor
M.D. Anderson Cancer Center · Other
Who this trial is looking for
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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.
Trial Locations
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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. …
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.
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