Cervical Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
This trial involves several different groups of people. Depending on which group applies, the criteria are:
Patients eligible for cervical cancer screening:
- People who currently live in the state of Texas
- People who receive care at a clinic that is partnering with this study
- Women and people who have a cervix
- People aged 25 to 65
- People who are due or overdue for a cervical cancer screening
Patients and community members for formative research:
- People who research staff have specifically identified as a relevant stakeholder for this part of the study
Healthcare providers, clinic staff, and health system stakeholders:
- People who work at least part-time at a health system that is partnering with this study, and who are aged 18 or older
Project ECHO participants:
- People who take part in at least one Project ECHO session, and who are aged 18 or older
Other clinical network participants:
- People who take part in at least one clinical network session, and who are aged 18 or older
Who may not be able to join:
For cervical cancer screening patients:
- People who are currently pregnant
- People who have had a complete hysterectomy (full surgical removal of the uterus)
- People who have a history of cervical cancer
For all other groups:
- People who are not able to communicate in English or Spanish
- Children, pregnant women, adults with cognitive impairment, or people who are currently incarcerated are not permitted to participate in any part of the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 713- 745-5008
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Safety and Adverse Events (AEs). Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 4.03
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.