Understanding Community-based HIV/AIDS Service Organizations: An Invaluable Source of HPV-related Cancer Information for At-risk Populations.
Lisa Tisdale WigfallPatricia GoodsonGeorge B CunninghamIdethia Shevon HarveyTamika D GilreathMaurice AdairBambi W GaddistCarmen Hampton JuliousDaniela B FriedmanPublished in: Journal of health communication (2020)
To describe non-clinical HIV service providers (NCHSPs) as surrogate seekers and health information mavens for people living with HIV (PLWH), men who have sex with men (MSM), and other vulnerable populations.In May/June 2016, we recruited 30 NCHSPs from three community-based HIV/AIDS service organizations. NCHSPs completed a 118-item self-administered, paper-and-pencil survey about HPV, cancer, and health communication. Data were analyzed using Stata/SE 14.1.Almost all (97%) NCHSPs were surrogate seekers and had looked for HIV/AIDS (97%), STD (97%), and cancer (93%) information. Most (60%) cancer information seekers had looked for information about HPV. The Internet (97%) and healthcare providers (97%) were health information sources almost all NCHSPs trusted. Nearly all NCHSPs (93%) were completely or very confident about their ability to find health information. The mean health information mavenism score (17.4 ± 2.1) was significantly higher than the scale's high-score cutoff (15.0) (p < 0 .001).NCHSPs look for and share health information with the vulnerable populations (e.g., PLWH, MSM) they serve. More research is needed to understand what NCHSPs' know and think about the health information they are sharing with vulnerable populations.
Keyphrases
- health information
- hiv aids
- healthcare
- social media
- men who have sex with men
- antiretroviral therapy
- papillary thyroid
- hiv testing
- hiv positive
- human immunodeficiency virus
- mental health
- hiv infected
- high grade
- childhood cancer
- public health
- genetic diversity
- climate change
- young adults
- cross sectional
- deep learning
- electronic health record
- affordable care act