MedPath

Fluid Intake Application to Reduce Kidney Stone Risks

Completed
Conditions
Kidney Stone
Interventions
Behavioral: iPhone Application
Behavioral: Android Application
Registration Number
NCT01928108
Lead Sponsor
University of North Carolina, Chapel Hill
Brief Summary

The purpose of this investigation is to prospectively evaluate the benefit of different methods of educating patients regarding their fluid intake through a readily available daily cellular phone application to improve overall urine output and reduce risk factors for stone recurrence.

Detailed Description

The prevalence of kidney stone disease in the United States is increasing. Recurrence of kidney stone disease has been reported as high as 50% at five years. Urine supersaturation is a predominant factor in the formation of crystallization and stone disease and is dependent on fluid volume. High fluid consumption that dilutes the urine has been shown both in vitro and in clinical studies to reduce the tendency for stone crystallization as well as effectively decrease stone recurrence. As a result, water intake greater than two liters per day is a common initial therapy for prevention of stone disease. However, studies have shown that despite physician counseling most patients are only able to modestly increase their urine volume through fluid intake. This finding may be due to a discrepancy in patient perception of their actual fluid intake and resulting urine volume. The purpose of this investigation is to prospectively evaluate the benefit of different methods of educating patient regarding their fluid intake through a readily available daily cellular phone application to improve overall urine output and reduce risk factors for stone recurrence.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  1. Patients ≥ 18 years old
  2. Seen in urology or nephrology clinic at UNC with a diagnosis of kidney stone
  3. Prior 24-hour urine result with volume less than 2 to 2.5 liters
Exclusion Criteria
  1. Patient without cellular phone capable of utilizing Android / Apple application
  2. Patient already using some form of monitoring fluid intake / volume
  3. Inability to take fluid by mouth
  4. Patient with urinary diversion, chronic diarrhea, bowel diversion or other forms of excessive fluid loss
  5. Inability to obtain informed consent
  6. Non-English speaking

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
iPhone ApplicationiPhone ApplicationParticipants using an iPhone will download the "waterlogged" application and use this to track daily water intake for 1 week.
Android ApplicationAndroid ApplicationParticipants using an Android cell phone will download the "water your body" application and use this to track daily water intake for 1 week.
Primary Outcome Measures
NameTimeMethod
24-hour urine volume7-10 days from baseline
Secondary Outcome Measures
NameTimeMethod
Actual 24-hour urine volume vs. patient perceived urine volume7-10 days from baseline
Ease and interest in monitoring fluid intake based on survey data7-10 days from baseline

Trial Locations

Locations (1)

North Carolina Memorial Hospital

🇺🇸

Chapel Hill, North Carolina, United States

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