RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2025-02-28
Study Completion:2027-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06754280

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.

Ages Eligible for Study:35 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-identifies as Black or African American
  2. * Age ≥35 to ≤80 years old
  3. * CKD Stage 1-4
  4. * Self-reported 6 or more hours/day of sedentary time
  5. * Ability to speak/read/understand English
  6. * Has access to a telephone
  1. * Being unable to walk 1 block
  2. * Being unable to stand from a seated position without assistance
  3. * Using a wheelchair, walker, or cane for all of their ambulation
  4. * 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
  5. * Kidney transplant
  6. * Any other condition that the investigator considers precludes participation in the trial
  7. * Participated in the Patient Advisory Board

Contacts and Locations

Study Contact

Mary Hannan, PhD
CONTACT
3123554838
mhanna22@uic.edu

Study Locations (Sites)

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

Collaborators and Investigators

Sponsor: University of Illinois at Chicago

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02-28
Study Completion Date2027-05

Study Record Updates

Study Start Date2025-02-28
Study Completion Date2027-05

Terms related to this study

Keywords Provided by Researchers

  • Sedentary

Additional Relevant MeSH Terms

  • Chronic Kidney Disease(CKD)