An Intervention to Reduce Sedentary Behavior for Black Adults with Chronic Kidney Disease

Description

RESET-CKD is evaluating an intervention to support Black adults with chronic kidney disease (CKD) to reduce their sedentary (e.g., sitting) time. Half of the participants will be randomized to the intervention, where the goal is to support individuals to reduce their sitting time, and the other half will be randomized to an attention control condition that provides CKD-related education not related to sedentary behavior. All participants will be followed for 12 weeks.

Conditions

Chronic Kidney Disease(CKD)

Talk to us

Study Overview

On this page

Study Details

Study overview

RESET-CKD is evaluating an intervention to support Black adults with chronic kidney disease (CKD) to reduce their sedentary (e.g., sitting) time. Half of the participants will be randomized to the intervention, where the goal is to support individuals to reduce their sitting time, and the other half will be randomized to an attention control condition that provides CKD-related education not related to sedentary behavior. All participants will be followed for 12 weeks.

Developing a Sedentary Reducing Intervention for Black Adults with CKD: RESET-CKD

An Intervention to Reduce Sedentary Behavior for Black Adults with Chronic Kidney Disease

Condition
Chronic Kidney Disease(CKD)
Intervention / Treatment

-

Contacts and Locations

Chicago

UI Health/University of Illinois Chicago, Chicago, Illinois, United States, 60612

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Self-identifies as Black or African American
  • * Age ≥35 to ≤80 years old
  • * CKD Stage 1-4
  • * Self-reported 6 or more hours/day of sedentary time
  • * Ability to speak/read/understand English
  • * Has access to a telephone
  • * Being unable to walk 1 block
  • * Being unable to stand from a seated position without assistance
  • * Using a wheelchair, walker, or cane for all of their ambulation
  • * Presence of a condition(s) or diagnosis, either physical or psychological, that precludes participation, including: Lower-extremity amputation (AKA or BKA) without prosthetic, Orthopedic condition that would preclude prompted sit-to-stand transitions or standing, Neurologic or psychiatric condition that would preclude prompted sit-to- stand transitions or standing, Severe cognitive impairment, Unstable coronary artery disease (i.e., angina with activity), Orthostatic hypotension
  • * Kidney transplant
  • * Any other condition that the investigator considers precludes participation in the trial
  • * Participated in the Patient Advisory Board

Ages Eligible for Study

35 Years to 80 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Illinois at Chicago,

Study Record Dates

2027-05