Video-Based Patient Navigation to Support Cervical Cancer Screening Among Black Women

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
ISA Associates, Inc.
Study ID
NCT07011836
Status
Recruiting
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Conditions

  • Uterine Cervical Neoplasms

Eligibility Criteria

Sex
FEMALE
Age
21 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • mNav Interactive Video + Navigator — BEHAVIORAL
    A personalized, video-based tool paired with navigator support to address individual screening barriers.
  • Educational Video — BEHAVIORAL
    A culturally tailored cervical cancer education video without additional support or tailoring.

Study Details

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

Key Dates

Start date
Jul 1, 2025
Status verified
Apr 2026
Primary completion
Jan 31, 2027
Completion
Mar 31, 2027

Study Design

Enrollment
288 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Experimental: Intervention Group
    Participants use an interactive, personalized video-based navigation tool (mNav) and receive navigator support.
  • Active Comparator: Education Control Group
    Participants view a general cervical cancer education video made for Black women, without personalized content or navigator support.

Primary Outcome Measure

Completion of Cervical Cancer Screening [ Time Frame: Within 6 months of enrollment ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Family and Medical Counseling Service, Inc.Washington D.C.District of Columbia20020
Vilma Kathy Argueta
[email protected]
(202) 800-4722
ISA AssociatesArlingtonVirginia22203
Mary Morcos, MPH
[email protected]
7032647223
Douglas Billings, PhD
[email protected]
7037390882

Find similar trials in Washington D.C., DC

By research site
Family and Medical Counseling Service, Inc.· Washington D.C., DCISA Associates· Arlington, VA

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