Novel Text-Messaging Bot in Patients Undergoing Joint Arthroplasty
Primary Purpose
Osteoarthritis, Knee, Osteoarthritis, Hip
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Automated Text Messaging (SMS) Bot (intervention group)
Routine perioperative education & teaching (control group)
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Total knee arthroplasty, Total hip arthroplasty
Eligibility Criteria
Inclusion Criteria:
- Inclusion criteria consisted of patients over 18 years of age, scheduled for primary total hip & knee arthroplasty, with smart phone capability, and proficiency in English.
Exclusion Criteria:
- Patients less than 18 years of age, no smart phone capability, poor English proficiency.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Text Messaging (SMS) Bot
Routine Perioperative Instructions
Arm Description
Patients undergoing total joint (hip & knee) arthroplasty will be enrolled in their physician's automated 'Text Messaging (SMS) Bot' in addition to receiving the routine perioperative education and instructions.
Patients undergoing total joint (hip & knee) arthroplasty will receive only their 'Routine Perioperative Instructions'.
Outcomes
Primary Outcome Measures
Time Participating in Home-Based Exercises
Stretching, strengthening, and other rehab-specific exercises counted toward their home-based exercises, while walking was excluded.
Secondary Outcome Measures
Knee Range of Motion
Degrees of flexion and extension of the operative knee will be measured at 3 and 6 weeks after surgery.
Use of Narcotics/Opiates
Medications designated as "narcotics" included any medications that contained: hydrocodone, oxycodone, codeine, morphine, or tramadol. Patients were instructed to record their responses during the same two-hour window each day in a daily diary.
Visual Analog Scale (VAS) mood score
VAS mood scores were collected from patients on the standard ten-point validated scale. If a patient circled two adjacent numbers on their daily diary, an average of the two numbers were assigned for that day.
Calls to the Office
The number of patient calls to their physicians office were tracked and recorded.
Patient Satisfaction
Patients were asked to fill out a satisfaction survey six weeks after surgery.
Visits to the Emergency Department (ED)
The number of visits to the ED were tracked and recorded.
Full Information
NCT ID
NCT03388502
First Posted
December 24, 2017
Last Updated
January 2, 2018
Sponsor
Rush University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03388502
Brief Title
Novel Text-Messaging Bot in Patients Undergoing Joint Arthroplasty
Official Title
Effectiveness of a Novel Text-Messaging Bot in Patients Undergoing Total Joint Arthroplasty: A Prospective Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
November 21, 2016 (Actual)
Primary Completion Date
August 1, 2017 (Actual)
Study Completion Date
October 1, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rush University Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the addition of an automated physician-specific text-messaging (SMS) bot in patients undergoing total joint arthroplasty. Half of the patients received the traditional perioperative education and instructions (control group), while the other half were enrolled in their physician's SMS bot (intervention group).
Detailed Description
In an era of value-based reimbursement and high-volume surgery, the patient experience is becoming increasingly important. Despite publicized efforts to place a greater emphasis on patient-centered care, patients often report poor access to their physician, lack of effective perioperative education, and frustration as their care is commoditized.
A text-messaging (SMS) bot has the potential to help fill some of these voids. Bots are computer programs that are inherently automated to simulate human-like tasks. While a physician may wish he or she could contact each of their patients daily, it would be an impossible undertaking for most. An SMS bot could make daily contact possible by automating it, potentially improving patient education and engagement before and after surgery. Standard SMS has been previously reported to be an effective means for delivering timely information, increasing patient compliance and outcomes (medication adherence, decrease surgical infections with antiseptic showers), and reaching a socioeconomically diverse patient population. Further benefits may be seen with an SMS bot due to its automated capabilities.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee, Osteoarthritis, Hip
Keywords
Total knee arthroplasty, Total hip arthroplasty
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
159 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Text Messaging (SMS) Bot
Arm Type
Experimental
Arm Description
Patients undergoing total joint (hip & knee) arthroplasty will be enrolled in their physician's automated 'Text Messaging (SMS) Bot' in addition to receiving the routine perioperative education and instructions.
Arm Title
Routine Perioperative Instructions
Arm Type
Active Comparator
Arm Description
Patients undergoing total joint (hip & knee) arthroplasty will receive only their 'Routine Perioperative Instructions'.
Intervention Type
Other
Intervention Name(s)
Automated Text Messaging (SMS) Bot (intervention group)
Intervention Description
Patients will be enrolled in an 'Automated Text Messaging (SMS) Bot (intervention group)' which is a computer program that sends patients timely reminders, instructions, and videos to help them prepare and recover from surgery.
Intervention Type
Other
Intervention Name(s)
Routine perioperative education & teaching (control group)
Intervention Description
Patients will receive the 'Routine perioperative education & teaching (control group)' and will not be enrolled in the physician-specific SMS bot.
Primary Outcome Measure Information:
Title
Time Participating in Home-Based Exercises
Description
Stretching, strengthening, and other rehab-specific exercises counted toward their home-based exercises, while walking was excluded.
Time Frame
over a six-week time period after arthroplasty surgery
Secondary Outcome Measure Information:
Title
Knee Range of Motion
Description
Degrees of flexion and extension of the operative knee will be measured at 3 and 6 weeks after surgery.
Time Frame
over a six-week time period after arthroplasty surgery
Title
Use of Narcotics/Opiates
Description
Medications designated as "narcotics" included any medications that contained: hydrocodone, oxycodone, codeine, morphine, or tramadol. Patients were instructed to record their responses during the same two-hour window each day in a daily diary.
Time Frame
over a six-week time period after arthroplasty surgery
Title
Visual Analog Scale (VAS) mood score
Description
VAS mood scores were collected from patients on the standard ten-point validated scale. If a patient circled two adjacent numbers on their daily diary, an average of the two numbers were assigned for that day.
Time Frame
over a six-week time period after arthroplasty surgery
Title
Calls to the Office
Description
The number of patient calls to their physicians office were tracked and recorded.
Time Frame
over a six-week time period after arthroplasty surgery
Title
Patient Satisfaction
Description
Patients were asked to fill out a satisfaction survey six weeks after surgery.
Time Frame
over a six-week time period after arthroplasty surgery
Title
Visits to the Emergency Department (ED)
Description
The number of visits to the ED were tracked and recorded.
Time Frame
over a six-week time period after arthroplasty surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Inclusion criteria consisted of patients over 18 years of age, scheduled for primary total hip & knee arthroplasty, with smart phone capability, and proficiency in English.
Exclusion Criteria:
Patients less than 18 years of age, no smart phone capability, poor English proficiency.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kevin J Campbell, MD
Organizational Affiliation
Rush University Medical Center
Official's Role
Study Director
12. IPD Sharing Statement
Learn more about this trial
Novel Text-Messaging Bot in Patients Undergoing Joint Arthroplasty
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