Comparing psychometric properties of two pain assessment scales
Phase 2
- Conditions
- pain.Pain, unspecified
- Registration Number
- IRCT2015062322881N1
- Lead Sponsor
- Vice chancellor for research, Ardabil University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients over 18 years old; Patients in intensive care units; patients on ventilators with endotracheal tube for more than 24 hours; able to listen and respond with shaking the head; eyebrows or eyes; the level of agitation and sedation between +1 and -3; according to Richmond Agitation Sedation Scale (RASS). Exclusion criteria: Patients with quadriplegia; those receiving muscular blocking agents or those with muscular dysfunction; Patients with Extensive injury in facial and arms; Patients with Drug addiction.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 15 minutes before non-nociceptive procedure, during non-nociceptive procedure, and 15 minutes after non-nociceptive procedure. Method of measurement: Two behavioural pain scales, BPS, NVPS.;Pain. Timepoint: 15 minutes before nociceptive procedure, during nociceptive procedure and 15 minutes after nociceptive procedure. Method of measurement: Two behavioural pain scales, BPS, NVPS.
- Secondary Outcome Measures
Name Time Method Physiological dimensions(Vital signs). Timepoint: 15 minutes before non-nociceptive procedure, during non-nociceptive procedure, and 15 minutes after non-nociceptive procedure. Method of measurement: Monitoring vital signs.;Physiological dimensions(Vital signs). Timepoint: 15 minutes before nociceptive procedure, during nociceptive procedure and 15 minutes after nociceptive procedure. Method of measurement: Monitoring vital signs.