Faith Moves Mountains: An Appalachian Cervical Cancer Prevention Project
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Sponsorii
Nancy Schoenberg
Colaboratori
National Cancer Institute (NCI)
STUDIU CLINIC: NCT01372241
BioSeek: NCT01372241
Cuvinte cheie
Abstract
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.
Descriere
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.
Datele
| Ultima verificare: | 05/31/2011 |
| Primul depus: | 06/07/2011 |
| Inscriere estimată trimisă: | 06/09/2011 |
| Prima postare: | 06/12/2011 |
| Ultima actualizare trimisă: | 04/19/2017 |
| Ultima actualizare postată: | 04/20/2017 |
| Data actuală de începere a studiului: | 11/30/2005 |
| Data estimată de finalizare primară: | 07/31/2009 |
| Data estimată de finalizare a studiului: | 07/31/2009 |
Stare sau boală
Cervical Cancer
Intervenție / tratament
Behavioral: Early Intervention
Fază
-
Grupuri de brațe
| Braţ | Intervenție / tratament |
|---|---|
| Experimental: Early Intervention This group served as the treatment group for analysis of the primary outcome. | Behavioral: Early Intervention The focus of the intervention was on reducing participants' self-identified barriers to obtaining Pap tests. |
| No Intervention: Delayed Intervention This group served as a wait-list control group, eventually receiving the intervention after the treatment group completed the intervention and the primary outcomes were assessed for both groups. |
Criterii de eligibilitate
| Vârste eligibile pentru studiu | 40 Years La 40 Years |
| Sexe eligibile pentru studiu | Female |
| Acceptă voluntari sănătoși | da |
| Criterii | 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 |
Rezultat
Măsuri de rezultate primare
1. Proportion of participants self-reporting receipt of Pap test [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.
