Clinical trial · Interventional
Promise Women Project
PROMIS WOMAN Education Program : ImProving ceRvical Cancer preventiOn Methods Among Muslim AmerIcans WOMEN
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer | Malignant Cervical Neoplasm | CURATED_EXACT | 0.92 |
| Human Papilloma Virus | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Promise women project (Promote Cervical Cancer Prevention Methods Among Muslim Women in Virginia ) | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- The single-arm trial with a pre- and post-test design
- description
- The Intervention Arm in the Promise Women Project evaluates a specific educational intervention program for Muslim women to promote cervical cancer prevention. It involves a one-time, 90-minute culturally and religiously tailored educational session with 20 participants. The session covers perceived risks of Human Papilloma Virus (HPV) infection, cervical cancer, and benefits of early screening and vaccination. Pre- and post-intervention surveys measure changes in participants' knowledge. This experimental arm assesses the intervention's effects on knowledge and acceptance of cervical cancer prevention.
- interventionNames
- Behavioral: Promise women project (Promote Cervical Cancer Prevention Methods Among Muslim Women in Virginia )
Primary outcomes (1)
- measure
- Number of Women Who Undergo Cervical Cancer Screening.
- timeFrame
- Baseline and Post Intervention (up to 1 week)
- description
- measured by tracking the number of women who schedule and attend
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available