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Active, Not Recruiting

NCT Number: NCT05355545

Virtually Supervised Exercise for Kidney Transplant Candidates

This study is examining whether a virtually supervised exercise program can improve physical function in persons who are awaiting kidney transplant. The investigators will compare the results to a similar group of persons who receive a health education program.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Conditions

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Stanford University

Palo Alto, California, 94304, United States

About this study

This study is examining if a virtually supervised exercise program can improve physical function in persons awaiting kidney transplant. A double-blind, parallel group randomized controlled clinical trial, this study will enroll 80 persons for 24 weeks. Our primary outcome is performance on the 30 second sit to stand test, and our secondary outcomes are changes in the Fatigue Severity Scale and the Beck Depression Inventory.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥ 18 years old
  • Listed for kidney transplant
  • Positive answers (e.g. yes) to one of the following:
  • current difficulty with climbing up 10 stairs,
  • has changed in the past year how they climb 10 stairs
  • current difficulty with walking a 0.5 mile (5-6 blocks)
  • has changed in past year in how they walk 0.5 mile (5-6 blocks)
  • documented performance of 430 meters or less on the six minute walk test in the past 12 months
  • documented performance of 9 points or less on the Short Physical Performance Battery in the past 24 months
  • documented performance of less than 3 points or less on the five times sit to stand test in the past 24 months
  • Demonstrated ability to stand up independently from a seated position and then sit back down without using their arms or an assistive device in the past 24 months

Exclusion criteria

  • Does not speak English or Spanish
  • Nursing home resident
  • Severe low vision (≥20/200 with corrective lens)
  • Severe hearing loss even with use of amplification preventing communication
  • Unstable angina or uncontrolled arrhythmia
  • Supplemental oxygen therapy
  • Myocardial infarction, major heart surgery, stroke, venous thromboembolism, hip fracture, hip or knee replacement in past six months (temporary exclusion)
  • ≥ 3 errors on the Six Item Screener

Treatment and study plan

Virtually supervised exercise

Behavioral

Participants will participate twice weekly in an live exercise program that they will access through a computer connected to the Internet.

Health Education

Behavioral

Participants will first participate in a once weekly live health education class that they will access through a computer connected to the Internet. During the second half of the study, participants will participate twice weekly in an live exercise program that they will access through a computer connected to the Internet.

Primary outcomes

  1. Change in performance on 30 second sit to stand test

    Time frame: Baseline through week 12

    Number of times that a person can stand up from a sitting position in 30 seconds

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
May 2, 2022
Registry last updated
Jul 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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