Clinical trial · Interventional
Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening
Feasibility of Community-based Distribution of HPV Self-Collection Kits for At Home Cervical Cancer Screening
NCT07453459CI-TRIAL-00119385recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer | Malignant Cervical Neoplasm | CURATED_EXACT | 0.92 |
| HPV Infection | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Qualitative Interview | Behavioral | — | UNRESOLVED |
| Virtual Visit Standard Instructions | Behavioral | — | UNRESOLVED |
| Virtual Visit Standard Instructions + In-Person Registration Navigation | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Aim 1: Standard instructions
- description
- Participants will complete a sociodemographic questionnaire and will receive the standard instructions. After approximately 8 weeks, participants will be asked to participate in the qualitative interview.
- interventionNames
- Behavioral: Qualitative Interview
- Behavioral: Virtual Visit Standard Instructions
- type
- EXPERIMENTAL
- label
- Aim 1: Standard instructions + in-person guidance
- description
- Participants will complete a sociodemographic questionnaire and will receive the standard instructions and in-person navigation for registering for a consult to receive the at-home testing kit. After approximately 8 weeks, participants will be asked to participate in the qualitative interview.
- interventionNames
- Behavioral: Qualitative Interview
- Behavioral: Virtual Visit Standard Instructions + In-Person Registration Navigation
Primary outcomes (8)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 25 Years
Show eligibility criteria text
Inclusion Criteria: * Are age 25 or older * Has an intact cervix * Self-reports that they have not been screened for cervical cancer within the last 3 years for 25-64, 5 years for 65 or older * Has a cellphone that can receive texts (including verification codes) and an email account * 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 Exclusion Criteria: * 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.
References
Publications (0)
Data not yet available
No reference posted for this study.