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Completed

NCT Number: NCT03164525

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

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.

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Key information

Conditions

Adult ICU Patients

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Faculty of Medicine Siriraj Hospital

Bangkok Noi, Bangkok, 10700, Thailand

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Critical care pain observation tool (CPOT)

Diagnostic Test

test validity and reliability of Thai-version CPOT and BPS

Other names: Behavioral pain scale (BPS)

Primary outcomes

  1. construct validity

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

Secondary outcomes

  1. content validity, concurrent validity, inter-rater reliability, and practicality

    Time frame: 24 hours after operation

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Official study title

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

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
May 23, 2017
Registry last updated
May 23, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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