RecruitingNot applicableFemale onlyEN originalCervical cancer

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

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

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.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Wiek od 21 do 65 lat
  • •Identyfikacja się jako osoba pochodzenia hispańskiego
  • •Nigdy nie robiona cytologia szyjki macicy lub ostatnia cytologia była 3 lub więcej lat temu
  • •Brak historii raka szyjki macicy
  • •Nie przebyta usunięcie macicy

✗ Disqualifies

  • •Poniżej 21 lat lub powyżej 65 lat
  • •Brak identyfikacji jako osoba pochodzenia hispańskiego
  • •Ostatnia cytologia szyjki macicy była wykonana mniej niż 3 lata temu
  • •Historia raka szyjki macicy
  • •Przebyta operacja usunięcia macicy

Simplified criteria — AI translation

Trial details

Minimum age
21 Years
Maximum age
65 Years
Last updated (source)
September 21, 2026
Sex
Female only

Therapies / drugs in trial

Locations (1)

Florida A&M University

Tallahassee, United States

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 9/12/2026.

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