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An Appalachian Cervical Cancer Prevention Project


N/A
40 Years
64 Years
Not Enrolling
Female
Cervical Cancer

Thank you

Trial Information

An Appalachian Cervical Cancer Prevention Project


Project development relied on principles of community based participatory research.
Participants were recruited from faith institutions in four distressed Appalachian Kentucky
counties. Investigators at the University of Kentucky worked closely with local staff who
implemented study procedures in the field.


Inclusion Criteria:



- Outside of cervical cancer screening guidelines at the time of study initiation

- Able to provide informed consent

Exclusion Criteria:

- History of cervical cancer

- History of hysterectomy

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Prevention

Outcome Measure:

Proportion of participants self-reporting receipt of Pap test

Outcome Description:

This measure is obtained at multiple timepoints during the study, but as the primary outcome it will be analyzed at the timepoint one month following the Early Intervention group's completion of the intervention.

Outcome Time Frame:

One month post-intervention

Safety Issue:

No

Principal Investigator

Nancy Schoenberg, Ph.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of Kentucky

Authority:

United States: Institutional Review Board

Study ID:

R01CA108696

NCT ID:

NCT01372241

Start Date:

December 2005

Completion Date:

August 2009

Related Keywords:

  • Cervical Cancer
  • Papanicolaou test
  • Cervical cancer screening
  • Randomized controlled trial
  • Faith-placed
  • Appalachia
  • Uterine Cervical Neoplasms

Name

Location

Faith Moves MountainsWhitesburg, Kentucky