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Clinical Trial Summary

Cervical cancer is a disease that is preventable through vaccination against the virus that causes it, human papillomavirus (HPV), and through screening and treatment of cervical disease before it becomes cancet.


Clinical Trial Description

Primary Objectives: The overall purpose of this protocol is to evaluate the feasibility and acceptability of CHW-delivered selfsample HPV testing (CHW-SS) to increase cervical cancer screening among women in RGV, a lowresource community in Texas. The specific aims of this protocol are to: Specific Aim 1: Determine the feasibility of CHW-SS in the RGV (i.e., reach, screening uptake, notification of test results). Specific Aim 2: Assess the acceptability and experiences of CHW-SS among under screened persons in rural, persistent poverty communities in the RGV. Secondary Objectives: Exploratory Aim 3: Assess attendance for clinical follow-up among individuals who participate in CHW-SS and test positive for HR-HPV. Exploratory Aim 4: Evaluate contextual fit of the intervention. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06109870
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Jane Montealegre, M D
Phone (281) 814-7118
Email jrmontealegre@mdanderson.org
Status Recruiting
Phase N/A
Start date October 30, 2023
Completion date August 31, 2030

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