Video and PDF for Knee Arthropathy

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Knee Arthropathy+4 MoreOpioid education in person - Other
Eligibility
18 - 80
All Sexes
What conditions do you have?
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Study Summary

The goal of this experimental study is to compare different education intervention on opioid education for patients undergoing total knee arthroplasty. The specific research questions to address are: Does perioperative education pathway reduce opioid refill requests? Is education pathway that focuses on pain management provided in-person and via video in repeated sessions more effective than current standard of care education consisting of a single exposure given as part of a broader preoperative presentation covering multiple topics? Is there a difference between education provided in-person vs video? Does perioperative education improve compliance with multimodal analgesia? Does perioperative education improve appropriate opioid storage? Does perioperative education improve appropriate opioid disposal? Enrolled patients will be assigned at random to one of 3 study groups. Group 1 (control): Patients are referred to the hospital's standard 1-hour virtual patient education webinar prior to surgery. Group 2 (in-person): Patients will receive two in-person education sessions (1st session before surgery and 2nd session after surgery). Patients will also receive portable document format (pdf) handouts about opioid and pain management. Group 3 (video): Patients will receive two video education sessions (1st session before surgery and 2nd session after surgery). Patients will also receive pdf handouts about opioid and pain management.

Eligible Conditions
  • Knee Arthropathy
  • Postoperative Pain
  • Opioid Use Disorder
  • Opioid Addiction
  • Opioid Abuse

Treatment Effectiveness

Effectiveness Progress

1 of 3

Study Objectives

2 Primary · 7 Secondary · Reporting Duration: Post-operative day 1, Post-operative day 7, Post-operative day 14

Week 1
Hospital length of stay
Post operative day (POD) 30
Opioid refill at POD 30
Post operative day (POD) 60
Opioid refill at POD 60
Day 14
Numerical Rating Scale
Opioid consumption
Day 14
Rates of compliance with multimodal regimen
Post-operative day 21
Opioids
Post-operative day 7
Rates of proper opioid storage
Day 14
Patient's health and recovery status following their surgery

Trial Safety

Safety Progress

1 of 3

Trial Design

3 Treatment Groups

Control Group
1 of 3
Video and PDF
1 of 3
In-person and PDF
1 of 3

Active Control

Experimental Treatment

36 Total Participants · 3 Treatment Groups

Primary Treatment: Video and PDF · No Placebo Group · N/A

Video and PDF
Other
Experimental Group · 1 Intervention: Opioid education via video · Intervention Types: Other
In-person and PDF
Other
Experimental Group · 1 Intervention: Opioid education in person · Intervention Types: Other
Control GroupNoIntervention Group · 1 Intervention: Control Group · Intervention Types:

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: post-operative day 1, post-operative day 7, post-operative day 14

Who is running the clinical trial?

Hospital for Special Surgery, New YorkLead Sponsor
225 Previous Clinical Trials
60,718 Total Patients Enrolled
1 Trials studying Knee Arthropathy
86 Patients Enrolled for Knee Arthropathy
Bradley H Lee, MDPrincipal InvestigatorHospital for Special Surgery, New York
1 Previous Clinical Trials
128 Total Patients Enrolled

Eligibility Criteria

Age 18 - 80 · All Participants · 3 Total Inclusion Criteria

Mark “Yes” if the following statements are true for you:
You are between the ages of 18 and 80 years old.
References