An Intervention to Reduce Sedentary Behavior for Black Adults With Chronic Kidney Disease
NCT ID: NCT06754280
Last Updated: 2025-07-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
40 participants
INTERVENTIONAL
2025-03-13
2027-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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RESET-CKD
RESET-CKD is a 12-week intervention that consists of four major components to support decreasing sedentary behavior: (1) health coaching, (2) feedback charts on sedentary behavior, (3) a workbook, and (4) reminders and cues.
RESET-CKD
RESET-CKD is a 12-week intervention that consists of four major components to support decreasing sedentary behavior: (1) health coaching, (2) feedback charts on sedentary behavior, (3) a workbook, and (4) reminders and cues.
Attention Control
CKD-related education
Attention Control
CKD-related education
Interventions
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RESET-CKD
RESET-CKD is a 12-week intervention that consists of four major components to support decreasing sedentary behavior: (1) health coaching, (2) feedback charts on sedentary behavior, (3) a workbook, and (4) reminders and cues.
Attention Control
CKD-related education
Eligibility Criteria
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Inclusion Criteria
* 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
Exclusion Criteria
* 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
35 Years
80 Years
ALL
No
Sponsors
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National Institute of Nursing Research (NINR)
NIH
University of Illinois at Chicago
OTHER
Responsible Party
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Mary Hannan
Assistant Professor
Locations
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UI Health/University of Illinois Chicago
Chicago, Illinois, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2024-1410
Identifier Type: -
Identifier Source: org_study_id
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