ERAS APPtimize: a mobile application to involve patients in the pathway of a intestinal surgery
Not Applicable
Completed
- Conditions
- <p>Colorectal surgery</p>10017998
- Registration Number
- NL-OMON29410
- Lead Sponsor
- Academic Medical Center (AMC), Department of Surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 140
Inclusion Criteria
- Individuals scheduled to undergo colorectal surgery due to:
o Inflammatory bowel disease
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Palliative surgery or surgery with additional radio- or chemotherapy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcome is the overall compliance to the ERAS protocol measured as a mean of the percentages of the single ERAS protocol elements which patients are actively involved in.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Postoperative data < 30 days<br /><br>Length of hospital stay<br /><br>Overall morbidity < 30 days<br /><br>Complications - major<br /><br>Complications - minor<br /><br>Reoperations<br /><br>Readmission <30 days<br /><br>In-hospital mortality<br /><br>Gastrointestinal<br /><br>Tolerate solid food<br /><br>Absence of nausea<br /><br>Passage of first flatus<br /><br>Passage of first stool<br /><br>Weight - preoperative<br /><br>Weight - at discharge<br /><br>Activity<br /><br>Mean preoperative physical activity<br /><br>Postoperative physical activity<br /><br>Fatigue<br /><br>Pain<br /><br>Perceived pain daily postoperative - discharge<br /><br>Compliance with intake of (pain) medication<br /><br>PROMS<br /><br>General quality of life<br /><br>Gastro-intestinal quality of life<br /><br>Physical Activity<br /><br>Patient satisfaction</p><br>