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Clinical Trials/NCT03764046
NCT03764046
Unknown
Not Applicable

Development and Validation of New "SNU Illustrated Pain Rating Scale" for Effective Assessment of Acute Postoperative Pain: a Comparative Study With Numeric Rating Scale

Seoul National University Hospital1 site in 1 country100 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain Measurement
Sponsor
Seoul National University Hospital
Enrollment
100
Locations
1
Primary Endpoint
Patient Satisfaction of Postoperative Pain Management
Last Updated
7 years ago

Overview

Brief Summary

The numeric rating scale (NRS), one of the most widely used pain scales in clinical practice, although convenient, is often subject to bias because it requires abstract thinking from both the patient and the evaluator. Compared to numbers, traumatic pain, when visualized appropriately, has potential advantage as a means to indicate and communicate the severity of pain. Given that they are standardized in terms of body parts, wound size, and bleeding volume, illustrations of traumatic pain along with external somatic stimuli that caused it can be used to serve as effective visual anchors to supplement a pain scale by giving more concrete information to the patient. The purpose of this study is to develop Seoul National University Illustrated Pain Scale(SNUIPS) using pictures of traumatic pain, and verify the validity and effectiveness of this scale in comparison with those of NRS.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
December 31, 2019
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jin-Tae Kim

Professor

Seoul National University Hospital

Eligibility Criteria

Inclusion Criteria

  • Adult patients undergoing a gynecological or orthopedic surgery under general anesthesia
  • Administered with intravenous patient-controlled analgesia for postoperative pain control
  • American Society of Anesthesiologists physical status class I-III patients

Exclusion Criteria

  • Contraindicated against fentanyl
  • Unable to communicate
  • Aged less than 18, or more than 79
  • Weighs less than 40kg or more than 89kg
  • Has severe heart disease(s)

Outcomes

Primary Outcomes

Patient Satisfaction of Postoperative Pain Management

Time Frame: 48 hours after surgery

Survey among patients on their level of overall satisfaction on postoperative pain management

Postoperative Pain Scores (NRS)

Time Frame: 48 hours after surgery

Self-reported pain intensity based on numeric rating scale evaluated after 48 hours after surgery for assessment of sensitivity to change. Each item is scored from 0 to 10 (0 = no pain; 10 = worst imaginable pain).

Postoperative Pain Scores (SNUIPS)

Time Frame: 48 hours after surgery

Self-reported pain intensity based on Seoul National University Illustrated Pain Scale evaluated after 48 hours after surgery. Each item is scored using illustrations that corresponds to 0-10 levels of traumatic pain, beginning from 'no injury and/or pain' to 'causalgia'.

Postoperative Consumption of Patient-Controlled and/or Rescue Analgesics

Time Frame: 48 hours after surgery

Amount of analgesics consumed through intravenous patient-controlled analgesia and/or administration of rescue analgesics

Understandability of Pain Scales

Time Frame: 48 hours after surgery

Survey among patients on understandability pain scales

Convenience of Pain Scales

Time Frame: 48 hours after surgery

Survey among patients on convenience of pain scales

Study Sites (1)

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