The effect of family educational on post operative pai
Phase 2
- Conditions
- Post operative pain.-
- Registration Number
- IRCT2016102816843N3
- Lead Sponsor
- Vice Chancellor for Research, Zanjan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Undergoing orthopedic surgery (upper or lower limbs); being older than 18 years; desire to participate in the study; ability to speak and read in Persian; healthy mental status; healthy visual status to see and understand VAS tool; being accompanied by a family member during hospitalization period. Exclusion criteria: history of previous surgeries; history of mental illnesses; using psychotropic drugs; history of drug abuse.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative pain. Timepoint: Every one hour during the waking time, for 2-3 days after surgery. Method of measurement: VAS (Visual analog Scale).
- Secondary Outcome Measures
Name Time Method Anexity. Timepoint: Before intervention and after second educational session. Method of measurement: Spielberger tool.