Impact of Ostom-i Alert Sensor on Quality of Life in Patients With Ileostomy

Not Applicable

Terminated

• Conditions: Ostomy
• Interventions: Other: No Ostom-i Alert Sensor; Device: Ostom-i Alert Sensor

• Registration Number: NCT02472639
• Lead Sponsor: Cedars-Sinai Medical Center

Brief Summary

The purpose of this study is to evaluate patient satisfaction and quality of life in patients with ileostomy managed with or without the novel Ostom-i Alert device.

Detailed Description

Patients with ileostomy have impaired quality of life related to their ileostomy (Person et al. DCR. 2012; 55: 783 - 787; Scarpa et al. Colorectal Dis. 2010; 12: 914 - 920). Although patients with ileostomy have better overall quality of life compared with colostomy patients (Silva et al. Worl J Surg. 2003; 27: 421-424), the liquid nature of the ileostomy effluent predisposes these patients to bag overfilling and dehydration more so than colostomy patients (Paquette et al. DCR 2013; 56: 974-979). This may be specifically important in populations with long term or permanent ileostomy. Overfilling and breakage/leakage of the ileostomy bag can also affect patient's ability to function in social environments, go out in public, have intimate relationships with significant others, and interfere with sleep patterns (due to high output and nighttime overfilling of the ileostomy bag).

The Ostom-i Alert is a novel device developed by a patient with ileostomy and now FDA approved in the United States. The device is a sensor that clips onto any ostomy bag and sends a Bluetooth signal to a mobile device app. An alarm lets the patient know before the stoma bag is at risk for overfilling and leaking. The potential advantage is that the device can prevent unexpected bag overfilling, breakage, and nighttime accidents. This may therefore lead to improved quality of life. The volume and output recordings can also be stored and emailed to the patient's health care providers, with potential to reduce ostomy related dehydration through more accurate volume recording and sharing.

While the device has many applications, the purpose of this research study is to specifically evaluate patient quality of life after application of the Ostom-i Alert compared with standard ostomy care.

Study Timeline

• Study Start: 2015-06-10
• Study First Submitted: 2015-06-12
• Study First Submitted QC: 2015-06-15
• Study First Posted: 2015-06-16
• Primary Completion: 2016-05-26
• Study Completion: 2016-05-26
• Results First Submitted: 2017-09-08
• Results First Submitted QC: 2017-09-08
• Status Verified: 2017-10
• Results First Posted: 2017-10-03
• Last Update Submitted: 2017-10-10
• Last Update Posted: 2017-11-09

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 7

Inclusion Criteria

1. Patients with ileostomies in place without a plan for ileostomy take down in the next 4 months.
2. Able to freely give written informed consent to participate in the study and have signed the Informed Consent Form;
3. Males or females, age 18 and older at the time of study screening;
4. Patients with loop or end ileostomy at least 1 month since ileostomy creation
5. No plan for stoma reversal for the next 4 months to allow adequate time for study inclusion
6. Patients who own an iPhone, iPod Touch, or Android device

Exclusion Criteria

1. Mentally incompetent or unable or unwilling to provide informed consent or comply with study procedures;
2. Children <18
3. Pregnant patients
4. Patients with planned ileostomy closure in the next 4 months
5. Patients with colostomy, more than one ostomy, or urostomy
6. Patients unable or unwilling to come in for in person Ostomi-I Alert teaching and screening visits
7. Patients without an iPhone, iPod Touch, or Android device

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
No Ostom-i Alert Sensor	No Ostom-i Alert Sensor	Patient will not wear Ostom-i sensor
Ostom-i Alert Sensor	Ostom-i Alert Sensor	Patients will wear Ostom-i sensor

Primary Outcome Measures

Name	Time	Method
Patient Quality of Life as Measured by the 20-item Stoma-QOL Questionnaire at 1 Month and 3 Month Follow-up After Using the Ostomi-I Alert Versus Standard Stoma Care Without the Ostom-i Alert.	up to 3 Months

Secondary Outcome Measures

Name	Time	Method
Overall Satisfaction With Ostom-i Device	3 months	Study was prematurely terminated. Data was not collected or analyzed due to issue with study compliance.
Number of Ostomy Bag Breakages During the Study Period	3 months	Study was prematurely terminated. Data was not collected or analyzed due to issue with study compliance.
Score on Additional QOL Questions Not Included in Stoma-QoL Questionnaire	3 months	Study was prematurely terminated. Data was not collected or analyzed due to issue with study compliance.
Dehydration Related Hospital Admissions During Study Period	3 months	Study was prematurely terminated. Data was not collected or analyzed due to issue with study compliance.