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Clinical Trials/NCT05862844
NCT05862844
Completed
Not Applicable

PROMIS WOMAN Education Program : ImProving ceRvical Cancer preventiOn Methods Among Muslim AmerIcans WOMEN

Mark Dignan, PhD4 sites in 1 country20 target enrollmentSeptember 25, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Human Papilloma Virus
Sponsor
Mark Dignan, PhD
Enrollment
20
Locations
4
Primary Endpoint
Number of Women Who Undergo Cervical Cancer Screening.
Status
Completed
Last Updated
last year

Overview

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 practice/communication skills training.
  • Provide feedback through satisfaction surveys. Researchers will compare participant outcomes before and after the intervention to assess its effectiveness. Additionally, the program's 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 women's 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.

Registry
clinicaltrials.gov
Start Date
September 25, 2023
End Date
October 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Mark Dignan, PhD
Responsible Party
Sponsor Investigator
Principal Investigator

Mark Dignan, PhD

Professor

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria:
  • Female Muslim individuals above 18 years old.
  • Able to speak and understand English.
  • Have not had a hysterectomy.
  • Have not had a cervical cancer diagnosis.
  • Willing to participate in the educational program and undergo cervical cancer screening.
  • Physically well, able to give consent form.

Exclusion Criteria

  • Under age 18
  • Not Muslim
  • Unable to provide consent
  • Participated in a pilot study

Outcomes

Primary Outcomes

Number of Women Who Undergo Cervical Cancer Screening.

Time Frame: Baseline and Post Intervention (up to 1 week)

measured by tracking the number of women who schedule and attend

Secondary Outcomes

  • Number of Women Enrolled(Baseline and Post Intervention (up to 1 week))

Study Sites (4)

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