New program aims to fight fatigue in kidney disease patients
NCT ID NCT06768983
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This small pilot study tested a cognitive behavioral program to help reduce fatigue in people with chronic kidney disease. Five adults with moderate-to-severe kidney disease took part in remote sessions. The goal was to see if the program was acceptable and to gather data for a larger future study.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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5 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Interest in participating in a fatigue study * Age ≥18 years old * Estimated glomerular filtration rate (eGFR) 15-44 mL/min/1.73 m2 * Ability and willingness to provide informed consent * Ability to speak English * Ability to walk * Ability to join remote study sessions via WebEx Exclusion Criteria: * Current involvement in an activity/exercise program * High likelihood of a kidney transplant within 6 months (assessed via the medical record) * Any safety concerns about increased walking (assessed via the medical record)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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NYU Langone Health
New York, New York, 10016, United States
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Other studies related to the condition(s) this trial covers.
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