Feasibility of Using sipIT Tools to Increase Compliance With Fluid Consumption Guidelines in Urolithiasis-Prone Subjects

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. The study aims to: 1) deliver notifications regarding fluid consumption to the FitBit Versa and the participant's smartphone based on the participant's assessed fluid intake, and 2) determine the acceptability of using the sipIT tools to increase fluid consumption. It is hypothesized that receiving notifications regarding fluid consumption will lead to an increased compliance in attaining fluid consumption guidelines. Further, it is hypothesized that the frequency of notifications will diminish across the study duration.

Key facts

Study ID

NCT03787615

Run by

Penn State University

People needed

31

Starts

2018-11-19

Expected to finish

2019-12-01

Last updated by the study team

2021-03-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Fluent in spoken and written English, and capable of providing informed consent
• Own an iPhone (version 6 or higher)
• History of urolithiasis
• Willingness to complete all study procedures: completing questionnaires, participating in semi-structured interviews, tracking fluid consumption, wearing a FitBit Versa and receiving notifications on the FitBit and their smartphone for a three-month period

You may not qualify if…

• Any medical condition that interferes with regular fluid consumption

Where it is running

• The Pennsylvania State University — University Park, Pennsylvania, United States

Full record on ClinicalTrials.gov

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