Pride in Prostate Care (PPC) collects various types of anonymous data to inform program development, evaluate its effectiveness, and contribute to the broader understanding of the unique experiences and needs of gay and transgender people with prostate cancer. The data collected is valuable for high-impact, peer-reviewed article creation, as it has the potential to fill knowledge gaps and inspire further research and clinical investigation.


Types of data that PPC collects include:

  1. Demographic data: Information about participants’ age, race, ethnicity, sexual orientation, and socioeconomic background can help identify potential disparities and trends in the population of gay men with prostate cancer.
  2. Clinical data: Information on the stage and type of prostate cancer, treatment options pursued, side effects experienced, and outcomes (e.g., survival rates, recurrence rates, quality of life) can help researchers understand the specific needs and challenges faced by this population and evaluate the effectiveness of the program.
  3. Patient-reported outcomes: Data on patient satisfaction with healthcare experiences, mental health, coping strategies, and overall quality of life can provide insights into the effectiveness of the culturally competent healthcare provider training, support groups, and online resource center.
  4. Provider-reported outcomes: Healthcare providers participating in the specialized training can report on their perceived improvements in cultural competence, changes in their approach to patient care, and any barriers they face in providing care to gay men with prostate cancer.
  5. Policy-related data: Information on changes in insurance coverage and healthcare policies at local, state, and federal levels can help evaluate the effectiveness of PPC’s policy advocacy efforts and their impact on access to care and support services.


By collecting and analyzing this data, PPC contributes to developing high-impact, peer-reviewed articles that address knowledge gaps and provide evidence-based recommendations for improving care and outcomes for gay men with prostate cancer. The data collected is used to:

  1. Assess the effectiveness of the program’s initiatives, leading to continuous improvement and refinement of the PPC program.
  2. Identify specific areas where interventions or policy changes have the most significant impact on reducing disparities and improving health equity.
  3. Contribute to the broader understanding of the unique needs and experiences of gay men with prostate cancer, fostering a more inclusive healthcare environment for this population.

Through the publication of high-impact articles, PPC raises awareness about the importance of addressing the unique needs of gay men with prostate cancer, inspires further research, and ultimately contributes to achieving greater health equity for all individuals affected by cancer.