Viewing Study NCT06350916



Ignite Creation Date: 2024-05-06 @ 8:21 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06350916
Status: COMPLETED
Last Update Posted: 2024-05-08
First Post: 2024-03-18

Brief Title: Application to Improve Patient Engagement and Decrease Postoperative Opioid Consumption in Patients for Colorectal Surgery
Sponsor: Wake Forest University Health Sciences
Organization: Wake Forest University Health Sciences

Study Overview

Official Title: An Educational Mobile Application to Improve Patient Engagement and Decrease Postoperative Opioid Consumption in Patients Enrolled in an Enhanced Recovery After Surgery ERAS Pathway for Colorectal Surgery
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate whether patient-centered educational material delivered before and immediately after surgery can help improve outcomes for patients undergoing colorectal surgery
Detailed Description: To analyze the impact of implementation of patient-centered educational material delivered the SeamlessMD mobile application on perioperative Enhanced Recovery After Surgery ERAS metric completion rates among patients undergoing elective colorectal surgery This is a non-interventional prospective feasibility study The planned study period will encompass adult patients 18 years scheduled to undergo an elective colorectal surgery procedure at CMC-Main during the six-month period of December 2020 to May 2021 Patients enrolling in SeamlessMD will be prompted by the mobile app to electronically complete a validated quality-of-life assessment the Quality of Recovery QoR-15 evaluation five days prior to surgery three days postoperatively and 30 days postoperatively

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
LCI-GI-CRC-SEAMLESS-2020 OTHER Atrium Health None