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Clinical Trials/NCT06350916
NCT06350916
Completed
Not Applicable

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

Wake Forest University Health Sciences1 site in 1 country75 target enrollmentJanuary 28, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Surgery
Sponsor
Wake Forest University Health Sciences
Enrollment
75
Locations
1
Primary Endpoint
30-day readmission
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 28, 2021
End Date
October 1, 2021
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patients (\>18 years old)
  • Scheduled to undergo an elective colorectal surgery procedure (for benign or malignant colon or rectal pathology) at CMC-Main by one of the 5 participating colorectal surgeons (Davis, Hill, Kasten, Salo, Squires)
  • Ability to provide informed consent

Exclusion Criteria

  • Emergent, non-elective colorectal procedures
  • Non-English speaking

Outcomes

Primary Outcomes

30-day readmission

Time Frame: 30 Days Following Hospital Discharge

Readmission to any hospital facility as inpatient within 30 days of surgery

Perioperative ERAS metric completion rate

Time Frame: 30 Days Following Hospital Discharge

Completion rate for perioperative ERAS metrics

Postoperative hospital length of stay

Time Frame: 30 Days Following Hospital Discharge

Postoperative hospital length of stay

Postoperative complications

Time Frame: 30 Days Following Hospital Discharge

Occurrence of postoperative complications within 30 days, classified as Clavien-Dindo Grade I-V

Secondary Outcomes

  • Postoperative Opioid Consumption(30 Days Following Hospital Discharge)

Study Sites (1)

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