Breast and Cervical Cancer Education Program
- Conditions
- Health BehaviorCervical CancerBreast Cancer
- Interventions
- Other: Educational Intervention
- Registration Number
- NCT06365450
- Lead Sponsor
- Johns Hopkins University
- Brief Summary
The primary goal of this study is to improve cancer literacy in Black women living with HIV and ultimately improve breast and cervical cancer screening uptake. This study involves an educational intervention delivered virtually and in person, depending on the participants' preference.
- Detailed Description
The aims of this study are to:
1. develop educational materials on breast and cervical cancer screening;
2. administer the intervention using a PowerPoint presentation;
3. evaluate changes in breast and cervical cancer literacy levels after the intervention; and
4. assess participants'; satisfaction with the program
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 60
- able to read and write in English
- self-identify as HIV positive -
- Black/African American.
- Acutely ill
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Educational Single-group Educational Intervention 1 educational session on cervical cancer and one educational session on breast cancer
- Primary Outcome Measures
Name Time Method Health Literacy in Cancer Screening as assessed by the Assessment of Health Literacy in Cancer Screening (AHL-C) tool. Immediately Post intervention The dimensions of health literacy adapted from the AHL-C tool are:
1. Numeracy (2 items)
2. Familiarity (9 items)
3. Comprehension (1 item)
4. Navigation (7 items).
To determine health literacy scores of participants, each item will be scored on a scale of 0 to 1. A higher score would mean a better outcome. Items will be summed for each of the four sub-scales as well as the entire scale (AHL-C) and then determine the mean and standard deviation.
Assessment will be completed immediately post intervention (after two sessions on breast and cervical cancer)
- Secondary Outcome Measures
Name Time Method Number of participants who preferred virtual or in person sessions Immediately Post intervention Participant session attendance preference
Number of participants recruited from each community partner Immediately Post intervention Participants recruited from each community partner
Number of participants who needed help redeeming their gift codes Immediately post intervention Participants needing help redeeming gift cards
Number of participants who were lost of follow up Immediately post intervention Participants lost to follow up
Trial Locations
- Locations (1)
Johns Hopkins University School of Nursing
🇺🇸Baltimore, Maryland, United States