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Measuring Physical Frailty in People Being Evaluated for a Kidney Transplant

Tracks physical performance in adults evaluated for kidney transplant, before and after surgery.

Plain-language title generated from the registry record
Registry title: Physical Performance Assessment in Kidney Transplant Evaluation

Key facts

Where
Martin, SlovakiaSee the site

Where in Slovakia

  • Transplant-nephrology departmentMartin, SlovakiaTaking people

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Trial details

Who runs it
University Hospital, Martin
Trial code
NCT07338929
Record updated
14 January 2026
Original description
This prospective cohort study investigates physical frailty, assessed by the Short Physical Performance Battery (SPPB), in patients evaluated for kidney transplantation. The study aims to compare SPPB scores before listing, annually during the waiting period, and after transplantation at 6 and 12 months. It also includes a control group of dialysis patients not eligible for transplantation to evaluate differences in physical performance. The goal is to understand how frailty impacts transplant outcomes and patient recovery.Read full original descriptionShow less

Physical Performance Assessment in Kidney Transplant Evaluation Using the Short Physical Performance Battery (SPPB)

This prospective cohort study investigates physical frailty, assessed by the Short Physical Performance Battery (SPPB), in patients evaluated for kidney transplantation. The study aims to compare SPPB scores before listing, annually during the waiting period, and after transplantation at 6 and 12 months. It also includes a control group of dialysis patients not eligible for transplantation to evaluate differences in physical performance. The goal is to understand how frailty impacts transplant outcomes and patient recovery.

Inclusion: Adult patients (≥18 years) undergoing evaluation for kidney transplantation; Patients on dialysis; Ability and consent to participate.

Exclusion: Acute medical conditions prohibiting SPPB assessment; Non-adult patients; Patients unable to provide informed consent.

ClinicalTrials.gov NCT07338929