Self-efficacy and pain control in the patients undergoing total knee arthroplasty

Not Applicable

• Conditions: Knee arthroplasty.; Presence of right artificial knee joint; Z96.651

• Registration Number: IRCT2015101224484N1
• Lead Sponsor: Vice Chancellor for Research of Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 98

Inclusion Criteria

Male and female patients aged 18 and over, patients undergoing total knee arthroplasty, patients with no history of chronic diseases and no drug addiction. Exclusion criteria: patient’s death, complications during and after surgery

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Self-efficacy. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: Pain Self-Efficacy Questionnaire.

Secondary Outcome Measures

Name	Time	Method
Pain control. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: Short-form McGill Pain Questionnaire.