Effectiveness of an eHealth Intervention for Uptake of Cervical Cancer Screening in Hispanic Women

StatusRecruiting
PhaseNot applicable
Started

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Record History

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  1. Minor Start date changed from estimate of Sep 21, 2026 to Oct 7, 2026
  2. Notable Lead sponsor: Florida A&M University to Florida A&M University Show 4 more changesShow less
    • Start date pushed from Sep 3, 2026 to Sep 21, 2026
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 2 of 2 entries
    • Site details revised
  3. Notable Recruitment opened
    • Study completion date: Sep 2029 to Sep 30, 2029
    • Start date changed from estimate of Jul 1, 2026 to Sep 3, 2026
    • Site details revised
    v2
  4. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study will test the effectiveness of an eHealth promotora (lay health advisor) outreach strategy to increase cervical cancer screening in Hispanic women. The investigators will recruit 160 Hispanic women ages 21-65 who are not up to date with cervical cancer screening or have never been screened, with the goal to evaluate screening knowledge, behavior, and intervention effects on cervical cancer screening outcomes. The study will utilize a two-arm, cluster randomized trial design, and participants will be randomly assigned to the cervical cancer education intervention or a nutrition education control group. The cervical cancer education arm will utilize a promotora to deliver an educational session virtually to encourage cervical cancer screening and receive a resource list for screening sites. The control group will participate in an educational session virtually about the importance of healthy nutrition. The primary study outcome is receipt of cervical cancer screening measured six months following receiving the intervention. The secondary outcomes will include cervical cancer screening knowledge and self-efficacy (confidence to receive cervical cancer screening). The research objective is to test the eHealth promotora intervention effectiveness for promoting cervical cancer screening in an under-screened Hispanic population.
Trial Details
NCT Number NCT06741241
Lead Sponsor Florida A&M University
Collaborators: National Institute on Minority Health and Health Disparities (NIMHD)
Conditions
(from sponsor)
Cervical Cancer Screening
Enrollment 170 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov