Ignite Creation Date:
2024-05-06 @ 7:00 PM
Last Modification Date:
2024-10-26 @ 2:58 PM
Study NCT ID:
NCT05862844
Status:
COMPLETED
Last Update Posted:
2023-12-06
First Post:
2023-05-08
Brief Title:
Promise Women Project
Sponsor:
Mark Dignan PhD
Organization:
University of Kentucky
Study Overview
Official Title:
PROMIS WOMAN Education Program ImProving ceRvical Cancer preventiOn Methods Among Muslim AmerIcans WOMEN
Status:
COMPLETED
Status Verified Date:
2023-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this study is to develop and test an intervention program to improve cervical cancer prevention among Muslim American women The main questions the investigators aim to answer are
Will the religiously tailored and culturally appropriate intervention program improve participants knowledge and acceptance of cervical cancer prevention
Is the intervention program feasible to conduct and acceptable to participants
Participants will be asked to
Attend focus group sessions to provide input on the development of educational materials
Complete pre- and post-intervention surveys to measure changes in knowledge and acceptance of cervical cancer prevention
Engage in the intervention program which includes education and experiential practicecommunication skills training
Provide feedback through satisfaction surveys Researchers will compare participant outcomes before and after the intervention to assess its effectiveness Additionally the programs feasibility and acceptability will be evaluated based on enrollment rates successful implementation participant engagement retention and satisfaction
Will the religiously tailored and culturally appropriate intervention program improve participants knowledge and acceptance of cervical cancer prevention
Is the intervention program feasible to conduct and acceptable to participants
Participants will be asked to
Attend focus group sessions to provide input on the development of educational materials
Complete pre- and post-intervention surveys to measure changes in knowledge and acceptance of cervical cancer prevention
Engage in the intervention program which includes education and experiential practicecommunication skills training
Provide feedback through satisfaction surveys Researchers will compare participant outcomes before and after the intervention to assess its effectiveness Additionally the programs feasibility and acceptability will be evaluated based on enrollment rates successful implementation participant engagement retention and satisfaction
Detailed Description:
This project involves creating special educational materials for Muslim women to learn about cervical cancer prevention The investigators will engage in discussions with 10 Muslim women during dedicated group sessions to ensure the suitability of the materials They will also seek input from Muslim religious leaders Subsequently they will conduct surveys before and after the program to assess the effectiveness of the materials in facilitating womens learning and comprehension of cervical cancer prevention To determine its efficacy and acceptability the investigators will implement the program with an additional 20 women and gather their feedback The goal of this project is to promote the health and well-being of Muslim women by providing them with culturally and religiously sensitive information regarding cervical cancer prevention
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 3P30CA177558-10S1 | NIH | None | httpsreporternihgovquickSearch3P30CA177558-10S1 |