Colorectal Surgery
Conditions
Keywords
ERAS, Enhanced recovery after surgery
Brief summary
The purpose of the study is to evaluate the value and effectiveness of a newly-implemented preoperative education class for patients undergoing colorectal surgery.
Detailed description
This is a non-randomized study to be conducted in a cohort of patients who are scheduled to undergo colorectal surgical procedures at Carolinas Medical Center (CMC)-Main. The primary objective of this study is to determine the effect of preoperative education classes on postoperative compliance with mobilization guidelines. Secondary objectives of this study are to evaluate the effect of the preoperative education class on patient knowledge, anxiety, and satisfaction, and postoperative outcomes such as inpatient length of stay, postoperative complications, and 30-day readmission rates. Data will be compared between patients who are scheduled to attend the class and attend and those who are scheduled to attend the class and do not.
Interventions
BEHAVIORALPreoperative education class
The preoperative enhanced recovery after surgery education class will be offered twice a week in coordination with anesthesia preoperative appointments to minimize inconvenience for patients. Patients will need to attend only one class. All participants will be offered the class. This class will be one hour in duration and will be taught by a surgical advanced care practitioner familiar with the details of colorectal surgery. The class will include detailed information about preoperative care, intraoperative care, and postoperative care.
BEHAVIORALPedometer
A pedometer will be affixed to patients in the immediate postoperative period and removed at time of discharge
Sponsors
Wake Forest University Health Sciences
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* Scheduled to undergo surgical operations of the colon or rectum at Carolinas Medical Center Main
Exclusion criteria
* A medical condition, laboratory finding, or physical exam finding that precludes participation * Develop a significant intra- or postoperative complication that precludes or delays participation for longer than 4 weeks; or * Have anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Time to ambulation | from time of surgery until the time of first documented ambulation, assessed up to 90 days | time to first ambulation following surgery measured by pedometer and notations made by nursing staff in the patient records prior to patient discharge. |
| Mean number of steps | from time of surgery until the time of discharge, up to 90 days | mean number of steps taken daily as measured by pedometer |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Patient satisfaction score | date of first postoperative follow-up appointment, up to 90 days following surgery | Patient satisfaction score assessed by satisfaction survey administered to patients |
| Knowledge level | date of preoperative education class (up to 2 weeks prior to time of surgery) and date of first postoperative follow-up appointment (up to 90 days following surgery) | Knowledge level assessed by knowledge survey administered to patients |
| Inpatient length of stay | from date of surgery until the date of discharge, up to 90 days | Inpatient length of stay measured in number of days |
| 30-day readmission rate | 30 days following surgery | — |
| Patient anxiety level | date of enrollment and date of discharge, up to 90 days following surgery | Patient anxiety level assessed by anxiety survey administered to patients |
Outcome results
None listed