Effectiveness of an EHealth Intervention for Uptake of Cervical Cancer Screening in Hispanic Women (NCT06741241)
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Florida A&M University — Tallahassee, Florida
Age range: 21 Years to 65 Years
🧪 Interventions in This Study
- eHealth Promotora (BEHAVIORAL)
- eHealth Healthy Nutrition (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Florida A&M University — Tallahassee, Florida
📞 Contact the Study Coordinator
Phone: (850) 599-3214
Email: tanise.jackson@famu.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Cervical Cancer Screening
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- Developing and Implementing HPV SCREENED — New Brunswick, New Jersey
- A Mobile Web App Intervention to Promote Cervical Cancer Screening — Lake Andes, South Dakota
- Personalized Risk-based Follow-up of Cervical Cancer Screening in Practice, RCT — Boston, Massachusetts
- Comparing Effectiveness of Physician-assisted Versus Self-assisted Pap Smear Collection — Atlanta, Georgia
Explore by condition: All Cervical Cancer Screening clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.