Our Work Experience
Needs Assessment to Support MASLD: A Call to Action initiative
We designed and executed a national needs assessment to identify where clinician practice diverges from current MASLD/MASH* guidance and where education could most effectively drive change. In total, 751 gastroenterologists, hepatologists, endocrinologists, and primary care providers completed the needs assessment survey. The findings identified participants’ knowledge gaps related to screening, diagnosis, and management of the diseases; benchmarked diagnostic and treatment patterns against practice guidance; and identified the educational needs to improve implementation of guideline-based treatment.
* Metabolic dysfunction-associated steatotic liver disease (MASLD) is formely known as nonalcoholic fatty liver disease or NAFLD); metabolic dysfunction-associated steatohepatitis (MASH) is formerly known as nonalcoholic steatohepatitis or NASH.
Strategic Stakeholder Mapping and Prioritization
We helped a global pharmaceutical company to assess the current state of medical education in obesity and prioritize opportunities to expand obesity education through medical professional associations with non-metabolic specialties, health systems, and universities in thirteen Northwestern European countries. We conducted in-depth interviews with internal stakeholders in each country, identified 34 organizations to profile, developed analytical framework, and conducted desk research and follow up interviews with organizations. In the end, we identified top advocates for medical education in obesity in each country and opportunities for direct and indirect collaboration with the pharmaceutical company.
C4C conducted similar studies with other audience segments (e.g., patient advocacy organizations, government agencies and regulatory bodies, multi-stakeholder alliances) internationally and domestically.
Mobile Point-of-Care App for the Index of Severity for Eosinophilic Esophagitis
We conducted usability testing of a new point-of-care mobile application that enables clinicians to calculate the Index of Severity for Eosinophilic Esophagitis (I-SEE). Sixty clinicians, including adult and pediatric gastroenterologists and allergists, used the app with EoE patients in routine practice and participated in in-depth qualitative interviews. Despite limited prior exposure to I-SEE, clinicians reported that the app was intuitive, easy to navigate, and could be completed in just minutes during clinical encounters, resulting in high satisfaction across specialties. Qualitative insights identified clear opportunities to further reduce friction and strengthen clinical impact, including design enhancements, electronic medical record integration, clarification of pediatric versus adult scoring, and stronger connections between severity scores and treatment decisions.
Confidence in Hereditary Cancer Discussion for Primary Care Providers
In partnership with the Family Medicine Education Consortium and the National Association of Chronic Disease Directors, we developed a seven-part, AAFP-accredited CME series to strengthen family physicians’ confidence and skills in identifying and managing patients at increased risk for hereditary breast cancer. The Confidence in Hereditary Cancer Discussion for Primary Care Providers series addresses common barriers to screening, referral, and patient communication. Each 15-minute module focuses on a key practice area, including using narrative medicine to discuss genetic risk, integrating screening and referral into primary care workflows, collaborating with genetic counselors, and supporting patients’ concerns around insurance, disclosure, and family communication.
Spotlight Case Study: Supporting CDC’s Bring Your Brave Campaign
We supported the CDC’s Bring Your Brave campaign to strengthen how healthcare providers identify, discuss, and manage hereditary cancer risk.
What we did
Led the development of digital resources, including a patient-provider conversation simulation, to support discussions about hereditary cancer risk, genetic testing, and family communication.
Convened and collaborated with professional medical associations, government partners, and nonprofit advocacy organizations to co-create campaign resources and expand dissemination.
In partnership with the Family Medicine Education Consortium, launched a Hereditary Breast Cancer Narrative Medicine Learning Collaborative for family medicine residents and faculty, integrating Bring Your Brave materials to improve awareness, communication skills, and patient engagement.
Developed and implemented a Quality Improvement (QI) initiative across seven family medicine clinics, supporting physicians and residents to screen for hereditary breast cancer risk, refer eligible patients to genetic counseling, and connect patients with Bring Your Brave educational resources following genetic testing (including BRCA1/BRCA2 results).
Impact
9+ million social media impressions
500,000+ patients and healthcare providers reached through partner outreach
Improved screening, referral, and communication practices across participating clinics
Awarded the 2023 Gold Anthem Award for health impact and excellence
Connect with us today to explore how we can develop a custom solution to help your organization advance its education, communication, and promotional goals.