Validation of the Thai Version CPOT and BPS in Postoperative ICU Patients

Adult ICU Patients Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03164525
• Other study ID #: Si553/2014
• Status: Completed
• Phase: N/A
• First received: May 22, 2017
• Last updated: May 22, 2017
• Start date: October 1, 2015
• Est. completion date: September 15, 2016

Study information

• Verified date: May 2017
• Source: Mahidol University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. completion date: September 15, 2016
• Est. primary completion date: July 15, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Adult ICU Patients

Intervention

Diagnostic Test:
• Critical care pain observation tool (CPOT)
test validity and reliability of Thai-version CPOT and BPS

Locations

Country	Name	City	State
Thailand	Faculty of Medicine Siriraj Hospital	Bangkok Noi	Bangkok

Sponsors (1)

Lead Sponsor	Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	construct validity		before and after analgesic given during 24 hours postoperative period
Secondary	content validity, concurrent validity, inter-rater reliability, and practicality		24 hours after operation