Ostom-i Alert Sensor Quality of Life Validation
Trial ID or NCT#
The purpose of this study is to determine the usability and acceptance of the Ostom-i Alert Sensor. The investigators would like to see if is generally helpful to ostomy patients and whether it has a beneficial impact on living with an ostomy bag. Results from this study will be used to determine if a larger clinical study is feasible.
Validating the Use of a Novel Wearable Device in Improving Quality of Life of Ostomy Patients
- - 18-80 years of age
- - use of an ostomy bag for at least six months
- - must own an iPhone, iPod Touch, or Android
- - use of large urostomy bags
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Dara Rouholiman, BS
About this Clinical Trial
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