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
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