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New treatment option for Cervical Cancer
Official title Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening
ClinicalTrials.gov ID: NCT07453459
What this study is testing
- What it's testing
- This study is testing and implementing an equity-focused, community-based intervention that improves women's access to cervical cancer screening and adherence to follow up after an abnormal result. The study's objective is to assess and compare the feasibility of different methods of distributing at-home HPV testing kits for cervical cancer screening among individuals who are under-screened.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 25 to 65, women only. Healthy volunteers may be eligible.
You may be able to join if
- Are age 25-65
- Has an intact cervix
- Self-reports that they have not been screened for cervical cancer within the last 3 years
- Has a smartphone
- Has access to the internet to engage with the Teal Health mobile app and complete a Zoom interview
You likely can't join if
- Abnormal vaginal bleeding or discharge
- A history of cancer of the reproductive system
- A compromised immune system
- Prior Diethylstilbestrol (DES) exposure
- Currently pregnant or are within 6 weeks of giving birth
- Treatment for a cervical precancer (e.g., loop electrosurgical excision procedure or conization) in the last 25 years.
See the full eligibility criteria
- Are age 25-65
- Has an intact cervix
- Self-reports that they have not been screened for cervical cancer within the last 3 years
- Has a smartphone
- Has access to the internet to engage with the Teal Health mobile app and complete a Zoom interview
- Can read, speak, write and understand English well enough to take a survey and complete an interview
- Abnormal vaginal bleeding or discharge
- A history of cancer of the reproductive system
- A compromised immune system
- Prior Diethylstilbestrol (DES) exposure
- Currently pregnant or are within 6 weeks of giving birth
- Treatment for a cervical precancer (e.g., loop electrosurgical excision procedure or conization) in the last 25 years.
The study team makes the final eligibility decision.
Where it's taking place
- St Louis, Missouri, 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, 25 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 St Louis, Missouri, 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.