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Clinical Trials/NCT03164525
NCT03164525
Completed
Not Applicable

Validation of the Thai Version Critical Care Pain Observation Tool and Behavioral Pain Scale in Postoperative Mechanically Ventilated ICU Patients

Mahidol University1 site in 1 country27 target enrollmentOctober 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adult ICU Patients
Sponsor
Mahidol University
Enrollment
27
Locations
1
Primary Endpoint
construct validity
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The prospective study set forth to test Thai version CPOT and BPS for validity, reliability, and practicality. After translation, both pain scales were tested for concurrent validity, discriminant validity, criterion validity, and inter-rater reliability in patients who were intubated during the postoperative period. Opinions regarding practicality were elicited via questionnaires from nurses who had been using and were familiar with these two pain scales.

Detailed Description

The prospective study set forth to test Thai version CPOT and BPS for validity, reliability, and practicality. After translation, both pain scales were tested for concurrent validity, discriminant validity, criterion validity, and inter-rater reliability in patients who were intubated during the postoperative period. Opinions regarding practicality were elicited via questionnaires from nurses who had been using and were familiar with these two pain scales.

Registry
clinicaltrials.gov
Start Date
October 1, 2015
End Date
September 15, 2016
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Karuna Wongtangman

MD

Mahidol University

Eligibility Criteria

Inclusion Criteria

  • aged ≥18 years
  • be able to communicate in Thai
  • intubated during postoperative period.

Exclusion Criteria

  • quadriplegia
  • patients with limb or facial injuries
  • patients receiving neuromuscular blockers
  • patients with limb mobility adversely affected by stroke
  • patients with epidural catheter used for postoperative pain control

Outcomes

Primary Outcomes

construct validity

Time Frame: before and after analgesic given during 24 hours postoperative period

Secondary Outcomes

  • content validity, concurrent validity, inter-rater reliability, and practicality(24 hours after operation)

Study Sites (1)

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