Actively Recruiting
Diaphragmatic Breathing Exercises As An Analgesia Adjunct in Total Knee Arthroplasty Patients in the Perioperative Period
Led by University of Southern California · Updated on 2024-08-27
50
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate diaphragmatic breathing exercises as a non-drug method to help manage pain after total knee arthroplasty, a common and often painful surgical procedure. The study focuses on patients undergoing this surgery at Keck USC Hospital, exploring whether these breathing exercises can improve pain control, reduce anxiety, and decrease opioid use during recovery. This pilot study will inform possible larger trials in the future. Participants will be taught diaphragmatic breathing exercises using handouts and videos before surgery and again in the recovery room. The study compares these participants' pain and anxiety levels, measured by the visual analog scale (VAS), and opioid consumption (morphine equivalents) to a control group of past patients who did not receive the breathing training. The control group data come from previous patients who had similar surgery and pain assessments but without the breathing intervention. During the study, pain, anxiety, and opioid use will be assessed at multiple timepoints: before the intervention, 15 minutes after, 6 hours after, and one day after. Researchers will monitor and compare these measures between the breathing exercise group and the control group. The total participation includes education before surgery, support in the recovery room, and follow-up assessments within one day. This observational study aims to understand how diaphragmatic breathing might support pain management after knee replacement surgery.
CONDITIONS
Brief Title
Diaphragmatic Breathing Exercises in Total Knee Arthroplasty Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing total knee arthroplasty with a continuous peripheral nerve block catheter
You will not qualify if you...
- Inability or unwillingness to perform diaphragmatic breathing exercises or participate in the study protocol
- Pregnant patients
- Patients without a continuous peripheral nerve block catheter
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From immediately post-surgery to 1 day after surgery
Participants perform diaphragmatic breathing exercises postoperatively as part of their pain management regimen.
1 baseline visit and multiple assessments within 1 day post-surgery
Duration - Up to 1 day after intervention
Participants’ pain, anxiety levels, and opioid usage are monitored after performing breathing exercises.
Assessments at 15 minutes, 6 hours, and 1 day after intervention
Trial Site Locations
Total: 1 location
1
Keck Hospital of USC
Los Angeles, California, United States, 90033
Actively Recruiting
Research Team
L
Linda J Rever, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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