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

Randomized controlled trial of comparison of the self-efficacy and pain control in the patients undergoing total knee arthroplasty with and without empowerment program

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015101224484N1

Enrollment

Registered

2016-03-15

Start date

2016-03-20

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Knee arthroplasty. Presence of right artificial knee joint

Interventions

Intervention 1: In the intervention group, an empowerment program based on Linton cognitive-behavior and Bandura behavior changing models will be used which is implemented for 6 weeks (one session bef

Behavior

In the intervention group, an empowerment program based on Linton cognitive-behavior and Bandura behavior changing models will be used which is implemented for 6 weeks (one session before surgery and

The control group receives no intervention

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

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

Secondary

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNazila Mir-Maroofi

Tabriz University of Medical Sciences

nmirmaroofi@yahoo.com+98 41 3347 7379

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026