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Observational for Cervical Cancer
N/A
Recruiting
Led By Brittany A. Strelow, DSMc, PA-C
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline
Awards & highlights
Study Summary
This study evaluates barriers to cervical cancer screening among non-compliant women.
Eligible Conditions
- Cervical Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Identify barriers to cervical cancer screening
Trial Design
1Treatment groups
Experimental Treatment
Group I: ObservationalExperimental Treatment1 Intervention
Participants complete a survey on study.
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Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,208 Previous Clinical Trials
3,567,050 Total Patients Enrolled
Brittany A. Strelow, DSMc, PA-CPrincipal InvestigatorMayo Clinic in Rochester
Frequently Asked Questions
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