grant

Developing and establishing the content validity of a patient reported experience measure for the kidney transplant evaluation process

Organization UNIVERSITY OF WASHINGTONLocation SEATTLE, UNITED STATESPosted 1 Sept 2025Deadline 31 Aug 2027
NIHUS FederalResearch GrantFY2025Access to CareAdvisory CommitteesAreaCaringCenters for Medicare and Medicaid ServicesClinicClinicalClinical ResearchClinical StudyCollaborationsCommittee MembersCommunitiesComplexConceptual DomainDevelopmentDialysisDialysis procedureEffectivenessEmotionalEquityEvaluationFamilyFamily memberFocus GroupsFundingFutureGoalsGrafting ProcedureHealth Care Financing AdministrationHealth Services AccessibilityIncentivesIndividualInterviewKidneyKidney DiseasesKidney FailureKidney GraftingKidney InsufficiencyKidney TransplantationKidney TransplantsKidney Urinary SystemLearningMeasuresMedical centerMethodologyNIDDKNational Institute of Diabetes and Digestive and Kidney DiseasesNational Institutes of HealthNephrologyNephropathyOrgan TransplantationOrgan TransplantsOutcomeOutcome MeasureParticipantPatient Outcomes AssessmentsPatient RecruitmentsPatient Reported MeasuresPatient Reported OutcomesPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatientsPersonsPhasePhonePhysical Phenomena or PropertiesPoliciesProcessProfessional OrganizationsRenal DiseaseRenal FailureRenal GraftingRenal InsufficiencyRenal TransplantationRenal TransplantsReportingResearchResearch ActivityResearch SupportReview LiteratureSocial WorkersStructureSurvey InstrumentSurveysTask ForcesTelephoneTestingTranscriptTransplant RecipientsTransplantationUnited States Centers for Medicare and Medicaid ServicesUnited States Health Care Financing AdministrationUnited States National Institutes of HealthUniversitiesValidationWaiting ListsWashingtonWorkaccess to health servicesaccess to servicesaccess to treatmentaccessibility to health servicesadvisory teamavailability of servicescandidate selectioncare accesscognitive interviewconferenceconventioncostdesigndesigningdevelopmentaldialysis therapyexperiencehealth service accesshealth services availabilityimprovedinstrumentintervention designkidney developmentkidney disorderkidney txmeasurable outcomemembernephrogenesisorgan allograftorgan graftorgan xenograftoutcome measurementparticipant engagementparticipant recruitmentpatient engagementpatient oriented outcomesperson centeredphysical processprofessional associationprofessional membershipprofessional societypsychosocialrecruitrenalrenal disordersecondary analysisservice availabilitysummitsymposiasymposiumtherapy designtransplanttransplant centerstransplant patienttransplant registrytreatment accesstreatment designvalidationswaitlist
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Full Description

PROJECT SUMMARY/ABSTRACT
Transplant is a valuable treatment option for many people with kidney failure, but in order to receive a kidney,

patients must first be referred to a transplant center and complete a process of physical and psychosocial

evaluation. Nephrologists and dialysis organizations are increasingly incentivized to refer greater numbers of

patients with kidney failure to transplant centers in an effort to improve equitable access to this treatment. Such

efforts can also be expected to increase the number and clinical complexity of patients engaging in the

evaluation process. However, many patients will not ultimately receive a kidney and the evaluation process

itself can be demanding, opaque, and lengthy and can take an emotional and psychosocial toll for patients and

families. As more patients are drawn into this care process, multiple national stakeholder groups have

emphasized the importance of minimizing burdens and improving patient experience. However, efforts to

improve this patient experience are hampered by a lack of validated measures. In recent years, leading

professional societies, regulators, and patient communities have called for the development of patient-reported

outcome measures of the pre-transplant process.

The aim of the proposed work is to develop and establish the content validity of a Kidney Transplant Evaluation

Patient Reported Experience Measure (KTE-PREM). In Phase 1 (concept elicitation), we will perform a

structured literature review, analyze existing qualitative interview transcripts, and conduct focus groups with

patients who were referred to a transplant center, their family members, and clinicians who care for these

patients (including primary nephrologists, social workers, and transplant team members). Patients will be

recruited from Northwest Kidney Centers (a large non-profit dialysis organization based in Washington state

which typically refers patients to three regional transplant centers) and the University of Washington. These

sequential steps will result in a comprehensive set of concepts potentially relevant to a KTE-PREM. In Phase 2

(concept prioritization), we will identify items most relevant to patients to be included in a KTE-PREM by

conducting a national survey among patients receiving care at two large non-profit dialysis organizations

(Northwest Kidney Centers and Dialysis Clinic, Inc) who were referred to a kidney transplant center. In Phase 3

(instrument construction and refinement), we will design a draft KTE-PREM and iteratively refine the instrument

through cognitive interviews with a local group of patients who were referred to a kidney transplant center.

The proposed work directly extends from Dr. Butler’s recent NIH/NIDDK supported research (K23DK129777),

which has identified a need and opportunities to improve person centricity of the kidney transplant evaluation

process. Following development of the KTE-PREM, additional funding will be sought for validation. We

anticipate that this validated instrument will have applications in clinical, research, and policy work intended to

measure and improve patient experience in the kidney transplant evaluation.

Grant Number: 1R03DK144242-01
NIH Institute/Center: NIH

Principal Investigator: Catherine Butler

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