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Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05196113
Study type Interventional
Source Penn State University
Contact
Status Active, not recruiting
Phase N/A
Start date January 4, 2022
Completion date June 15, 2025

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