Israni, Ajay K.Bruin, MarilynChu, SaumanMcKinney, Warren T.Schaffhausen, CorySchladt, David2024-08-152024-08-152024-08-15https://hdl.handle.net/11299/264970This record contains supplemental files only; they are the discussion guide used for interviews and focus groups. demographic/clinical questionnaire used for kidney patients, and demographic/clinical questionnaire used for the family members of kidney patients. The original data is sensitive in nature and will not be shared under any circumstances. It is preserved at the Principal Investigator's institution.Choosing a transplant center that will accept a particular candidate can be difficult and challenging for patients with end-stage organ failure. As transplant centers have varying levels of expertise, interests, and outcomes of solid organ transplant, patient health-related characteristics influence the variation in candidates centers will accept. Most transplant candidates undergo waitlist work-ups as outpatients and many undergo transplant at centers not closest to their homes. Some are listed at more than one center. Several studies suggest that patients have a choice of centers. The PI, as Deputy Director of the Scientific Registry of Transplant Recipients (SRTR), provides comparative information to the public about each solid organ transplant center in the United States. The risk adjusted outcomes, in the report cards, account for the transplant recipient's health-related characteristics, donor characteristics and transplant related factors. Many transplant centers provide a print-out of this SRTR report card to their candidates to comply with Centers for Medicare & Medicaid rules. Unfortunately, in their current format, the report cards are not designed for transplant candidates, many of whom may have low health literacy and numeracy. The proposed work aims to develop and evaluate a patient-centered website and printouts of the SRTR report cards that will effectively communicate comparative information to transplant candidates about their alternatives when choosing transplant centers. We will develop a novel tool to allow candidates to tailor the report cards to their clinical profiles based on their health-related characteristics and to communicate information on alternative transplant centers that perform transplants in patients like them. The website will also allow patients to self-refer to centers. Here, we provide copies of the interview / focus group guide as well as examples of the demographic / clinical questionnaires completed by study participants. We are releasing these materials to allow for greater insight into the study and to enhance reproducibility.Attribution-NonCommercial 4.0 InternationalOrgan TransplantationPatient-centeredQualitativeDecision MakingDatasethttps://doi.org/10.13020/BAGF-H278