Effects of Thrice Weekly versus Home Dialysis on Cardiovascular Functional Capacity (ELDEN) Study

K
Kenneth Lim

Primary Investigator

Overview

The aim of this study is to compare the effects of home dialysis, peritoneal dialysis, and conventional three times a week dialysis on cardiovascular functional capacity (the parts of your body including the heart, blood vessels, and lungs that move air around your body and helps remove waste products).

All visits will take place in the cardiopulmonary exercise testing (CPET) lab and Fit Core which are located on the 5th floor of IU University Hospital.  Each study visit will take approximately 3 hours.  You will be required to also participate in the Musculoskeletal Function, Imaging and Tissue Resource Core (FIT) Core study.

Description

What is involved if i participate?
  • If you are determined to be eligible, your participation in the study would involve 2 separate outpatient visits (3 hrs each) at the Indiana Clinical Research Center at IU-Health University Hospital at 550 University Boulevard in Indianapolis. 
  • Each visit will occur after dialysis or on a non-dialysis day and will be 12 months apart.
  • Study visits will include the following: questionnaires, hand grip test, repeated chair stands, walking and balance tests, a cycling bike exercise test, echo (ultrasound of your heart), whole body fluid status with electric device (painless), and blood draws.
Will I be compensated?
  • Participants will receive a total of $200.00 for participation
How can I participate?

Eligibility

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    chronic kidney disease, CKD
  • Age: Between 18 Years - 100 Years
  • Gender: All

Inclusion Criteria:
  • All patients age 18 years or older.
  • All races and ethnicities. Both genders.
  • CKD stage 5D patients.
  • English speaking patients.
Exclusion Criteria:
  • Patients with malignancy requiring chemotherapy or metastatic disease.
  • Patients unable to exercise due to musculoskeletal issues.
  • Patients likely to not be available to complete all protocol-required study visits or procedures, and/or to comply with all required study procedures to the best of the patient, research team and Investigator’s knowledge.
  • Patients with active implanted medical devices (e.g. cardiac pacemaker, defibrillators).
  • Pregnancy or breastfeeding.
  • Weight > 300 pounds.

Updated on 04 May 2024. Study ID: 12808, NEPH-IIR-ELDEN
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Interested in the study?

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