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NCT03787615 · ClinicalTrials.gov registry record · NA
Feasibility of Using sipIT Tools to Increase Compliance With Fluid Consumption Guidelines in Urolithiasis-Prone Subjects
A NA study of Urolithiasis, sponsored by Penn State University.
- Completed
- Registry status
- NA
- Development phase
- 31
- Enrollment target
- 1
- Study location
NCT03787615 is a NA study of Urolithiasis that has completed, run by Penn State University. The registered enrollment target is 31 participants, below the 378-participant average among 11 other Urolithiasis trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03787615, a NA study of Urolithiasis, has completed, sponsored by Penn State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 31 participants
- Enrollment target
- 1
- Study location
Study 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. 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.
Conditions Studied
Interventions
- DEVICE sipIT tools
Study Locations (1)
Pennsylvania
- The Pennsylvania State University - University Park
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 31 participants |
| Start Date | 2018-11-19 |
| Est. Completion | 2019-12-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03787615
The ClinicalTrials.gov registry entry for NCT03787615 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 378-participant average among 11 other Urolithiasis trials with a reported enrollment target (92% lower). The listed sponsor is Penn State University, which has 219 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urolithiasis appearing as the primary indexed condition, and to 1 intervention - of which sipIT tools is the first listed.
NCT03787615 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT03787615 about?
NCT03787615 is a clinical study titled "Feasibility of Using sipIT Tools to Increase Compliance With Fluid Consumption Guidelines in Urolithiasis-Prone Subjects". 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) deliv...
What is the current status of trial NCT03787615?
This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2018-11-19. Estimated completion is 2019-12-01.
What conditions does trial NCT03787615 study?
This clinical trial studies the following conditions: Urolithiasis.
What interventions are being tested in trial NCT03787615?
The interventions under investigation include: sipIT tools (DEVICE).
Who is sponsoring clinical trial NCT03787615?
This trial is sponsored by Penn State University, which has 219 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03787615 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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