Recruiting

mNav & In-Person Navigation

Sponsor:

ISA Associates, Inc.

Code:

NCT07011836

Conditions

Uterine Cervical Neoplasms

Eligibility Criteria

Sex: Female

Age: 21 - 65

Healthy Volunteers: Not accepted

Interventions

mNav Interactive Video + Navigator

Educational Video

Study Details

Brief summary:

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

Conditions

Uterine Cervical Neoplasms

Study ID

NCT07011836

Start date

Jul 1, 2025

Status verified date

Apr, 2026

Completion date

Mar 31, 2027

Anticipated

Primary completion date

Jan 31, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 21 - 65

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

288 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

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.

Interventions

mNav Interactive Video + Navigator

A personalized, video-based tool paired with navigator support to address individual screening barriers.

Educational Video

A culturally tailored cervical cancer education video without additional support or tailoring.

Primary outcome measure

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

Central Contacts and Locations

Central contacts

Locations

Family and Medical Counseling Service, Inc.

Recruiting

Washington D.C., District of Columbia, United States, 20020

Contacts

More Information

Sponsor

ISA Associates, Inc.

Last update posted

Apr 21, 2026

Last verified

Apr, 2026

Keywords

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

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by ISA Associates, Inc. on 2026-04-21.