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Ostom-i Alert Sensor Quality of Life Validation
Trial ID: NCT02319434
Purpose
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.
Official Title
Validating the Use of a Novel Wearable Device in Improving Quality of Life of Ostomy Patients
Stanford Investigator(s)
Lawrence Chu, MD, MS
Professor of Anesthesiology, Perioperative and Pain Medicine
Eligibility
Inclusion Criteria:
- 18-80 years of age
- use of an ostomy bag for at least six months
- must own an iPhone, iPod Touch, or Android
Exclusion Criteria:
- use of large urostomy bags
Intervention(s):
device: Ostom-i Alert Sensor
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Dara Rouholiman, BS
6507236632