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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03164525
Enrollment
27
Registered
2017-05-23
Start date
2015-10-01
Completion date
2016-09-15
Last updated
2017-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult ICU Patients

Keywords

Thai version, validated, Critical Care Pain Observation Tool, Behavioral Pain Scale, adult ICU patients

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.

Interventions

DIAGNOSTIC_TESTCritical care pain observation tool (CPOT)

test validity and reliability of Thai-version CPOT and BPS

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
construct validitybefore and after analgesic given during 24 hours postoperative period

Secondary

MeasureTime frame
content validity, concurrent validity, inter-rater reliability, and practicality24 hours after operation

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026