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Clinical Trials/NCT01372241
NCT01372241
Completed
Not Applicable

An Appalachian Cervical Cancer Prevention Project

Nancy Schoenberg1 site in 1 country345 target enrollmentDecember 2005
ConditionsCervical Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervical Cancer
Sponsor
Nancy Schoenberg
Enrollment
345
Locations
1
Primary Endpoint
Proportion of participants self-reporting receipt of Pap test
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to determine whether a faith-placed lay health advisor intervention is effective in increasing use of Pap smears among middle-aged and older Appalachian women.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
December 2005
End Date
August 2009
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Nancy Schoenberg
Responsible Party
Sponsor Investigator
Principal Investigator

Nancy Schoenberg

Sponsor/PI

University of Kentucky

Eligibility Criteria

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

Outcomes

Primary Outcomes

Proportion of participants self-reporting receipt of Pap test

Time Frame: One month post-intervention

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.

Study Sites (1)

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