Video-Based Patient Navigation to Support Cervical Cancer Screening Among Black Women
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: mNav Interactive Video + Navigator, Educational Video.
- Who it may be relevant to
- Registry conditions: Uterine Cervical Neoplasms. Basic parameters: 21 years — 65 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Enhancing the Effectiveness of Community Health Workers to Reduce Cervical Cancer Disparities in African American Women
Overview
The goal of this clinical trial is to test whether an interactive, video-based patient navigation program can improve cervical cancer screening among African American women who are currently overdue for screening. The main questions it aims to answer are: Can an interactive video navigation tool (mNav), when paired with in-person navigation, improve screening adherence compared to a standard educational video alone? Does the intervention improve knowledge, reduce barriers, and increase intentions to get screened? Researchers will compare participants who receive both the interactive video (guided by an on-screen navigator) and in-person navigation to those who receive only a standard educational video to see if the tailored support increases screening rates. Participants will: Complete two phone surveys (one at the beginning and one six months later) Be randomly assigned to one of two groups: One group will receive an interactive video experience tailored to their concerns plus support from an in-person navigator The other group will receive a standard educational video designed for African American women Have their clinic records reviewed six months later to check for cervical cancer screening completion
Interventions
- Behavioral mNav Interactive Video + Navigator
A personalized, video-based tool paired with navigator support to address individual screening barriers. - Behavioral Educational Video
A culturally tailored cervical cancer education video without additional support or tailoring.
Primary outcome measures
- Completion of Cervical Cancer Screening [Time frame: Within 6 months of enrollment]
Secondary outcome measures (2)
- Cervical Cancer Screening Intention [Time frame: Baseline and 6-month follow-up]
- Cervical Cancer Knowledge Scale [Time frame: Baseline and 6-month follow-up]
Eligibility criteria
Inclusion criteria
- Black or African American woman
- Nonadherent to USPSTF cervical cancer screening guidelines (no Pap test in the past 3 years or no HPV test in the past 5 years)
- Age 21 to 65 years old
- Not currently pregnant
- No history of hysterectomy
- Access to a mobile phone capable of receiving text messages and watching video content
Exclusion criteria
\*None
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Prevention
Study locations
United States · 2 centers
- Family and Medical Counseling Service, Inc. — Washington D.C.
- ISA Associates — Arlington
Identifiers
NCT: NCT07011836 · MD015221 · 5R44MD015221-04