Cervical Cancer Screening Project Part C

Stopped early

Conditions studied: Cervical Cancer

In brief

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.

Key facts

Study ID

NCT01575444

Run by

University of Minnesota

People needed

10

Starts

2012-06-01

Expected to finish

2014-05-01

Last updated by the study team

2017-12-12

Who can join

Age: 25 and older, up to 70. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Somali female age 25-70 years
• have lived in the U.S. 10 years or less
• have not had a Pap test (by self report) in the last 3 years

You may not qualify if…

• Women with a self reported past history of any of the following will not be eligible:
• total hysterectomy
• cervical cancer
• active history of cervical dysplasia

Where it is running

• Masonic Cancer Center, University of Minnesota — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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