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Evaluation of a Preoperative Education Class for Colorectal Surgery Patients

Withdrawn
Conditions
Colorectal Surgery
Interventions
Behavioral: Pedometer
Behavioral: Preoperative education class
Registration Number
NCT03237897
Lead Sponsor
Wake Forest University Health Sciences
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.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Scheduled to undergo surgical operations of the colon or rectum at Carolinas Medical Center Main
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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.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Class non-attendeesPedometerA cohort of patients who are scheduled to undergo colorectal surgical procedures and do not attend the scheduled preoperative education class. Patients will be affixed with a pedometer in the postoperative period until discharge.
Class attendeesPedometerA cohort of patients who are scheduled to undergo colorectal surgical procedures and attend the preoperative education class. Patients will be affixed with a pedometer in the postoperative period until discharge.
Class attendeesPreoperative education classA cohort of patients who are scheduled to undergo colorectal surgical procedures and attend the preoperative education class. Patients will be affixed with a pedometer in the postoperative period until discharge.
Primary Outcome Measures
NameTimeMethod
Mean number of stepsfrom time of surgery until the time of discharge, up to 90 days

mean number of steps taken daily as measured by pedometer

Time to ambulationfrom 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.

Secondary Outcome Measures
NameTimeMethod
Patient satisfaction scoredate of first postoperative follow-up appointment, up to 90 days following surgery

Patient satisfaction score assessed by satisfaction survey administered to patients

Knowledge leveldate 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

Patient anxiety leveldate of enrollment and date of discharge, up to 90 days following surgery

Patient anxiety level assessed by anxiety survey administered to patients

30-day readmission rate30 days following surgery
Inpatient length of stayfrom date of surgery until the date of discharge, up to 90 days

Inpatient length of stay measured in number of days

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