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Breast and Cervical Cancer Education Program

Not Applicable
Completed
Conditions
Health Behavior
Cervical Cancer
Breast 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
Inclusion Criteria
  • able to read and write in English
  • self-identify as HIV positive -
  • Black/African American.
Exclusion Criteria
  • Acutely ill

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Educational Single-groupEducational Intervention1 educational session on cervical cancer and one educational session on breast cancer
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
Number of participants who preferred virtual or in person sessionsImmediately Post intervention

Participant session attendance preference

Number of participants recruited from each community partnerImmediately Post intervention

Participants recruited from each community partner

Number of participants who needed help redeeming their gift codesImmediately post intervention

Participants needing help redeeming gift cards

Number of participants who were lost of follow upImmediately post intervention

Participants lost to follow up

Trial Locations

Locations (1)

Johns Hopkins University School of Nursing

🇺🇸

Baltimore, Maryland, United States

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