This study will be the third phase of a larger study intended to increase screening for cervical cancer among women of Mexican descent who are rarely or never screened.
AIM 1: To examine the efficacy of the AMIGAS program.
AIM 2: To characterize the effectiveness of the major components of the program (with promotoras).
AIM 3: To conduct a process evaluation to ensure appropriate delivery of the intervention.
AIM 4: To conduct a cost-effectiveness analysis of the intervention to assess: Recruit 200 women of Mexican origin (who are not compliant with CC screening guidelines) from each of three areas: 1. El Paso (US-México border) 2. Houston (urban) 3. Yakima Valley, Washington (rural).
For more information on this project, contact the Principal Investigator:
Theresa L. Byrd
Centers for Disease Control and Prevention