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Novel Text-Messaging Bot in Patients Undergoing Joint Arthroplasty

Effectiveness of a Novel Text-Messaging Bot in Patients Undergoing Total Joint Arthroplasty: A Prospective Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03388502
Enrollment
159
Registered
2018-01-03
Start date
2016-11-21
Completion date
2017-10-01
Last updated
2023-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Hip, Osteoarthritis, Knee

Keywords

Total knee arthroplasty, Total hip arthroplasty

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.

Interventions

OTHERAutomated Text Messaging (SMS) Bot (intervention group)

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.

OTHERRoutine perioperative education & teaching (control group)

Patients will receive the 'Routine perioperative education & teaching (control group)' and will not be enrolled in the physician-specific SMS bot.

Sponsors

Rush University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Time Participating in Home-Based Exercisesover a six-week time period after arthroplasty surgeryStretching, strengthening, and other rehab-specific exercises counted toward their home-based exercises, while walking was excluded.

Secondary

MeasureTime frameDescription
Use of Narcotics/Opiatesover a six-week time period after arthroplasty surgeryMedications 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 Score6 weeks post-operativeVAS 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. Minimum score 0. Maximum score 10. Higher score is worse outcome (more pain).
Knee Range of Motionover a six-week time period after arthroplasty surgeryDegrees of flexion and extension of the operative knee will be measured at 6 weeks after surgery.
Number of Participants Reporting Satisfaction With Instruction Clarityover a six-week time period after arthroplasty surgeryPatients were asked to fill out a satisfaction survey six weeks after surgery
Visits to the Emergency Department (ED)over a six-week time period after arthroplasty surgeryThe number of visits to the ED were tracked and recorded.
Calls to the Officeover a six-week time period after arthroplasty surgeryThe number of patient calls to their physicians office were tracked and recorded.

Participant flow

Participants by arm

ArmCount
Text Messaging (SMS) Bot
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. Automated Text Messaging (SMS) Bot (intervention group): 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.
76
Routine Perioperative Instructions
Patients undergoing total joint (hip & knee) arthroplasty will receive only their 'Routine Perioperative Instructions'. Routine perioperative education & teaching (control group): Patients will receive the 'Routine perioperative education & teaching (control group)' and will not be enrolled in the physician-specific SMS bot.
83
Total159

Baseline characteristics

CharacteristicRoutine Perioperative InstructionsText Messaging (SMS) BotTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
28 Participants20 Participants48 Participants
Age, Categorical
Between 18 and 65 years
55 Participants56 Participants111 Participants
Age, Continuous60.9 years
STANDARD_DEVIATION 8.2
59.3 years
STANDARD_DEVIATION 8
60.2 years
STANDARD_DEVIATION 8.1
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Sex: Female, Male
Female
36 Participants35 Participants71 Participants
Sex: Female, Male
Male
47 Participants41 Participants88 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 760 / 83
other
Total, other adverse events
0 / 760 / 83
serious
Total, serious adverse events
0 / 764 / 83

Outcome results

Primary

Time Participating in Home-Based Exercises

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

ArmMeasureValue (MEAN)Dispersion
Text Messaging (SMS) BotTime Participating in Home-Based Exercises46.4 minutesStandard Deviation 17.4
Routine Perioperative InstructionsTime Participating in Home-Based Exercises37.7 minutesStandard Deviation 16.3
Secondary

Calls to the Office

The number of patient calls to their physicians office were tracked and recorded.

Time frame: over a six-week time period after arthroplasty surgery

ArmMeasureValue (MEAN)Dispersion
Text Messaging (SMS) BotCalls to the Office0.6 number of callsStandard Deviation 0.8
Routine Perioperative InstructionsCalls to the Office2.6 number of callsStandard Deviation 3.4
Secondary

Knee Range of Motion

Degrees of flexion and extension of the operative knee will be measured at 6 weeks after surgery.

Time frame: over a six-week time period after arthroplasty surgery

ArmMeasureValue (MEAN)Dispersion
Text Messaging (SMS) BotKnee Range of Motion111.9 degreesStandard Deviation 13.3
Routine Perioperative InstructionsKnee Range of Motion108.0 degreesStandard Deviation 12.8
Secondary

Number of Participants Reporting Satisfaction With Instruction Clarity

Patients were asked to fill out a satisfaction survey six weeks after surgery

Time frame: over a six-week time period after arthroplasty surgery

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Text Messaging (SMS) BotNumber of Participants Reporting Satisfaction With Instruction Clarity69 Participants
Routine Perioperative InstructionsNumber of Participants Reporting Satisfaction With Instruction Clarity38 Participants
Secondary

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.

Time frame: over a six-week time period after arthroplasty surgery

ArmMeasureValue (MEAN)Dispersion
Text Messaging (SMS) BotUse of Narcotics/Opiates22.5 daysStandard Deviation 13.4
Routine Perioperative InstructionsUse of Narcotics/Opiates32.4 daysStandard Deviation 11.8
Secondary

Visits to the Emergency Department (ED)

The number of visits to the ED were tracked and recorded.

Time frame: over a six-week time period after arthroplasty surgery

ArmMeasureValue (NUMBER)
Text Messaging (SMS) BotVisits to the Emergency Department (ED)0 visits
Routine Perioperative InstructionsVisits to the Emergency Department (ED)4 visits
Secondary

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. Minimum score 0. Maximum score 10. Higher score is worse outcome (more pain).

Time frame: 6 weeks post-operative

ArmMeasureValue (MEAN)Dispersion
Text Messaging (SMS) BotVisual Analog Scale (VAS) Mood Score7.5 score on a scaleStandard Deviation 1.8
Routine Perioperative InstructionsVisual Analog Scale (VAS) Mood Score6.5 score on a scaleStandard Deviation 1.7

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026