Assessing Dermatological Health Needs in Rural Communities

Background: Rural communities face significant barriers to dermatologic care, including geographic isolation and financial constraints. These challenges contribute to delayed diagnoses and suboptimal management of skin conditions, exacerbating health disparities. Rural student-run free clinics (SRFCs) provide essential dermatologic services to underserved populations, but limited data exist on the specific dermatologic needs and care barriers faced by these communities. This study aims to assess the dermatologic health needs, care barriers, and healthcare-seeking behaviors of patients attending an SRFC serving a rural population. Methods: An anonymous 19-question survey was distributed via REDCap to individuals aged 18 and older attending a rural SRFC. The survey collected data on demographics, dermatologic conditions, access to care, treatment and prevention strategies, and sources of dermatologic health education. Descriptive statistics were used to analyze trends in dermatologic care access, financial barriers, and information-seeking behaviors. Results: Among 42 participants, 26% were aged 26–35, and 69% identified as female. Acne (38.5%) and eczema (23.1%) were the most commonly reported conditions. Only 60% of those with a diagnosed condition had confirmed access to dermatologic care. Income did not correlate with care access (Spearman r = 0.27, p = 0.189). Geographic barriers persisted, as 50% of respondents were uncertain whether dermatology services were available locally. Younger participants (18–35) primarily relied on internet searches and social media for dermatologic information, while older participants (56+) consulted healthcare providers. Among participants earning $60,000–$90,000, 100% had access to dermatologic care, but 75% had never sought care regularly. Uncertainty about access was highest among lower-income groups. Conclusions: Rural populations experience significant uncertainty about dermatologic care availability, contributing to delayed treatment. Financial barriers and reliance on non-medical information sources hinder effective care utilization. Targeted educational initiatives and improved access strategies, such as SRFCs, can reduce care disparities.