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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
Rush University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Total knee arthroplasty, Total hip arthroplasty

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    December 24, 2017
    Last Updated
    January 2, 2018
    Sponsor
    Rush University Medical Center
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    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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