MedTrace Logo

Cervical Cancer Screening Project Part C

NCT01575444 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2017-12-12

No results posted yet for this study

Summary

This proposal has been developed through collaboration between the University of Minnesota and New American Community Services (NACS), and the research design is based on a needs assessment conducted by the community partner. The investigators will test the hypotheses that women who are offered home vaginal bio-specimen collection will have higher rate of cervical cancer screening completion than that of women referred for clinic-based Pap test. All participants will be given identical education materials on cervical cancer screening and HPV, currently in use by the Minnesota Sage Program.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Rahel Ghebre, M.D. · Masonic Cancer Center, University of Minnesota

Eligibility

Min Age
25 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2014-05-31
Completion
2014-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01575444 on ClinicalTrials.gov