RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Enhancing the Effectiveness of Community Health Workers to Reduce Cervical Cancer Disparities in African American Women

Quick Facts

Study Start:2025-06-24
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07011836

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 65 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Black or African American woman
  2. * Nonadherent to USPSTF cervical cancer screening guidelines (no Pap test in the past 3 years or no HPV test in the past 5 years)
  3. * Age 21 to 65 years old
  4. * Not currently pregnant
  5. * No history of hysterectomy
  6. * Access to a mobile phone capable of receiving text messages and watching video content
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Douglas Billings, PhD
CONTACT
7037390882
dbillings@isagroup.com

Study Locations (Sites)

Family and Medical Counseling Service, Inc.
Washington, District of Columbia, 20020
United States
ISA Associates
Arlington, Virginia, 22203
United States

Collaborators and Investigators

Sponsor: ISA Associates, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-06-24
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2025-06-24
Study Completion Date2026-06-30

Terms related to this study

Keywords Provided by Researchers

  • Early Detection of Cancer
  • Health Behavior
  • Patient Navigation
  • African Americans

Additional Relevant MeSH Terms

  • Uterine Cervical Neoplasms