Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2216 participants
OBSERVATIONAL
2023-03-23
2023-10-28
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Observational
Participants complete a survey on study.
Non-Interventional Study
Non interventional study
Interventions
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Non-Interventional Study
Non interventional study
Eligibility Criteria
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Inclusion Criteria
* Non-compliant for cervical cancer screening within Mayo Clinic Primary Care
Exclusion Criteria
* Complaint for cervical cancer screening within Mayo Clinic Primary Care
* Women who decline participation
21 Years
65 Years
FEMALE
Yes
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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Brittany A. Strelow, DSMc, PA-C
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic in Rochester
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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NCI-2024-00181
Identifier Type: REGISTRY
Identifier Source: secondary_id
22-004500
Identifier Type: OTHER
Identifier Source: secondary_id
22-004500
Identifier Type: -
Identifier Source: org_study_id
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