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OpenTrials
Completed

NCT Number: NCT06284447

Barriers to Cervical Cancer Screening

This study evaluates barriers to cervical cancer screening among non-compliant women.

Completed

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Key information

About this study

PRIMARY OBJECTIVE:

I. To further identify barriers to cervical cancer screening in women, we will identify non-compliant patients and survey them to better understand barriers that have led to inadequate screening.

OUTLINE: This is an observational study.

Participants complete a survey on study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women between the ages of 21-65
  • Non-compliant for cervical cancer screening within Mayo Clinic Primary Care

Exclusion criteria

  • Women less than 21 or older than 65
  • Complaint for cervical cancer screening within Mayo Clinic Primary Care
  • Women who decline participation

Treatment and study plan

Non-Interventional Study

Other

Non interventional study

Primary outcomes

  1. Identify barriers to cervical cancer screening

    Time frame: Baseline

    Participants will receive a brief "Pap Smear Barriers Survey" (likely completed in 5-15 minutes) which asks yes/no/no preference questions regarding potential barriers to cervical cancer screening. Responses will be compared regionally and by Mayo Clinic Health System site.

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Feb 29, 2024
Registry last updated
May 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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