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N/A Completed N=20 Prevention

Promise Women Project

Human Papilloma Virus · Cervical Cancer
Source: ClinicalTrials.gov NCT05862844 ↗
Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcomePrimary: Number of Women Who Undergo Cervical Cancer Screening. — 20 Participants

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Women Who Undergo Cervical Cancer Screening.
20
SECONDARY
Number of Women Enrolled
20

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05862844). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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