Loading clinical trials...
Loading clinical trials...
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.
The study uses a randomized controlled trial design with a 12-month intervention period and outcome assessments at baseline, 1, 3, and 12 months. Participants will be randomly assigned to groups. Both groups will receive usual care which involves education about fluid intake guidelines and encouragement to adhere to those guidelines from a clinician. The intervention group will additionally receive the sipIT intervention comprising a semi-automated fluid intake tracking system and context-sensitive, just-in-time notifications reminding them to drink.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
University of Michigan
Ann Arbor, Michigan, United States
Penn State Hershey Medical Center
Hershey, Pennsylvania, United States
Start Date
January 4, 2022
Primary Completion Date
April 28, 2025
Completion Date
April 28, 2025
Last Updated
September 16, 2025
216
ACTUAL participants
sipIT
BEHAVIORAL
Lead Sponsor
University of Michigan
Collaborators
NCT07275879
NCT06158620
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions