Tele-monitoring of Post Join Arthroplasty Outcomes: A Feasibility Study

Not Applicable

Completed

• Conditions: Post-Op Complication
• Interventions: Other: Telemedicine

• Registration Number: NCT04586296
• Lead Sponsor: University of Alabama at Birmingham

Brief Summary

The purpose of this study is to develop an effective telephone mediated follow-up system to reduce the number of unplanned readmissions and emergency department visits after total joint arthroplasty. This will help reduce costs related to unnecessary visits to the hospital as well as catch complications earlier on. The investigators plan to accomplish this by performing a pilot study that will compare the outcomes of using an Interactive Voice Response system through phone call in addition to the standard follow-up protocol. The outcomes of this group will be compared to those receiving the standard of care follow-up protocol.

Detailed Description

Upon patient education and consent to participate in this study, patients will be randomized via online randomizer during their baseline visit into either Treatment As Usual (TAU) or Integrated Voice Response (IVR) cohorts. During this baseline visit, the patients in the IVR group will be given specific information on the nature of the calls and what to expect. Both groups will fill out a form for assessing their baseline pain and functionality. Both groups will receive standard total joint arthroplasty. After this, the TAU group will receive the standard of care which involves appropriate pain management and scheduled clinic follow-ups lasting approximately 60 minutes at 2 weeks, 6 weeks, and 12 weeks along with additional visits if required. Clinic visits will assess pain via VAS scale, joint functionality via HOOS and KOOS scale, and quality of life via SF-36.

In addition to the standard of care follow-up visits as in the TAU group, the IVR group will also receive automated phone calls lasting up to 3 minutes, which will be the focus of this research study. These phone calls will be daily for the first week, every other day the second week, twice a week for weeks 3-6, and weekly for weeks 7-12. The content of these calls will assess pain management, wound healing and screen for potential complications through a series of questions (questionnaire script attached). At the completion of each call, the patient will be instructed to either continue standard treatment or visit the emergency department based on the content of their response. If there is reason for concern, the PI will automatically be informed.

Survey questions pertaining to the patients outcomes and satisfaction will be completed in clinic and collected by the PI. The responses and data relating to IVR calls will made available through computer software designed by our team on the secure REDcap network.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2020-10-06
• Study First Submitted QC: 2020-10-13
• Study First Posted: 2020-10-14
• Study Start: 2021-03-16
• Status Verified: 2023-08
• Primary Completion: 2023-08-15
• Last Update Submitted: 2023-08-15
• Study Completion: 2023-08-16
• Last Update Posted: 2023-08-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

• Participants eligible to undergo the TJA surgical procedure

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Exclusion Criteria

• Participants who are not eligible to undergo the TJA surgical procedure

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Telemedicine Group	Telemedicine	Group that will be receiving the telemedicine intervention in addition to the standard of care post-op.

Primary Outcome Measures

Name	Time	Method
Percentage of Patients with acceptable joint functionality as measured by hip disability and osteoarthritis outcome score (HOOS)	12 weeks	HOOS is a patient measured scores evaluating Hip function and creates a score out of 100, 100 indicating full functionality.
Percentage of Patients with acceptable quality of life as measured by Short Form Health Survey SF-36	12 weeks	The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability.
Percentage of Patients with acceptable pain control as measured by Visual Analogue scale	Baseline	VAS is a patient measured scale to evaluate pain, on a scale of 1-10 with 10 being the worst pain.
Percentage of Patients with acceptable joint functionality as measured by hip disability and osteoarthritis outcome score (HOOS) and knee disability and osteoarthritis outcome score (KOOS)	Baseline	KOOS is a patient measured score evaluating Hip function and creates a score out of 100, 100 indicating full functionality.
Percentage of Patients with acceptable joint functionality as measured by knee disability and osteoarthritis outcome score (KOOS)	12 weeks	KOOS is a patient measured score evaluating Hip and knee function and creates a score out of 100, 100 indicating full functionality.

Trial Locations

Locations (1)

UAB Highland Hospital; 🇺🇸 Birmingham, Alabama, United States