Aim 1: Data collection methods, timing, and measures | |
Pre-site visit phone interviews—once at baseline | Organizational structure, key stakeholders, practice champion |
Approaches to delivery of adolescent preventive care services (such as immunizations) | |
Formal site visit—once at baseline | Baseline workflows; baseline patient data collection: eligible patient population, patient demographics, and other characteristics of the patient population; baseline immunization rates; baseline community partnership data: existing education programs and efforts and existing partnerships; use of ALERT IIS and EHR to capture and track immunizations |
Practice survey (PS)—once at baseline | Practice and practice’s patient demographics, practice change, payer mix, revenue and payments, and HPV vaccine priority |
ALERT IIS—at baseline | Patient demographics (age, race/ethnicity, vaccination status, insurance status, and other covariates) |
Aim 2: Data collection methods, timing, and measures | |
Quality Improvement Change Questionnaire (QICA)—every 12 months | Engaged leadership |
Organized, evidence-based care; quality improvement strategy; continuous and team-based healing relationships; care coordination | |
Site visits—monthly, for 18 months | Workflows; patient data collection: eligible patient population, patient demographics, and other characteristics of the patient population; quarterly immunization rates; quarterly community partnership data: existing education programs and efforts; existing partnerships |
Intervention data entries—monthly | PDSA cycle worksheets, workflow mapping, field notes |
Practice survey (PS), administered as needed to reflect change | Practice and practice’s patient demographics, practice change, payer mix, revenue and payments, HPV vaccine priority |
ALERT IIS—quarterly | Patient demographics (age, race/ethnicity, vaccination status, insurance status, and other covariates) |
Aim 3: Data collection methods, timing, and measures | |
Pre- and post-community partner group interviews | Acceptability of HPV vaccination |
Patient/parent surveys—every 6 months | Child and parents’ knowledge about cancer risk reduction and the HPV vaccine series; where and how information about HPV and cancer risk reduction via vaccination was sought; demographic information |