sipIT2: Improving Adherence to Fluid Intake Guidelines for Kidney Stone Prevention
Completed · Not applicable
Conditions studied: Urolithiasis
In brief
The purpose of this study is to examine the feasibility of using sipIT tools (i.e., wrist-worn sensors, smart water bottles, mobile applications) to increase compliance with physician-recommended fluid consumption guidelines in participants with a history of urolithiasis.
Key facts
- Study ID
- NCT05196113
- Run by
- University of Michigan
- People needed
- 216
- Starts
- 2022-01-04
- Expected to finish
- 2025-04-28
- Last updated by the study team
- 2025-09-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- previous diagnosis of symptomatic kidney stone in past 5 yrs
- 24-hr urine volume ≤ 2.0 L/day,
- age 18 or older,
- own iOS or Android smartphone,
- proficient in English language,
- capable of providing informed consent, and
- willing to use a Fitbit smartwatch, connected water bottle, and mobile app for the study every day for a year, and receive text messages reminder to drink.
You may not qualify if…
- previous diagnosis with cystine stone,
- pregnant or planning to become pregnant in the next 12 months,
- concurrently participating in another study involving fluid intake or diet,
- plan to have surgery or relocate outside the area within the next year
- co-morbidities that preclude high fluid intake, conditions with high fluid losses (e.g., congestive heart failure, bariatric surgery, GI tract ostomy, short gut syndrome, chronic diarrhea including patients with ulcerative colitis/Crohn's disease, hyponatremia), or conditions that preclude ability to collect 24-hour urine (severe urinary incontinence),
- active medical treatments that would impair protocol compliance,
- chronic use of lithium, or
- psychiatric conditions impairing compliance with the study protocol.
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States
- Penn State Hershey Medical Center — Hershey, Pennsylvania, United States
Full record on ClinicalTrials.gov
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