BridgeMD
Tests treatment safety and results for HR-HPV Testing
Official title Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems
ClinicalTrials.gov ID: NCT06843720
What this study is testing
- What it's testing
- 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.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65, women only. Healthy volunteers may be eligible.
You may be able to join if
- Populations involved in the research are:
- stakeholder advisory board members;
- patients eligible for cervical cancer screening participating in the cluster assigned by chance stepped-wedge trial;
- patients and community members participating in formative research activities;
- providers, clinic staff, and other health system stakeholders from partnering health systems;
You likely can't join if
- 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...
See the full eligibility criteria
- Populations involved in the research are:
- stakeholder advisory board members;
- patients eligible for cervical cancer screening participating in the cluster assigned by chance 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+
- 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...
The study team makes the final eligibility decision.
Where it's taking place
- Houston, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Houston, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.