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The effect of Rehabilitation Education in patients Who undergo a Total knee Replacement

The effect of Rehabilitation Education on surgical outcomes in patients Who undergo a Total knee Replacement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091124002769N6
Enrollment
96
Registered
2018-06-18
Start date
2017-09-22
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

knee replacement in osteoarthritis patient. Primary generalized (osteo)arthrosis

Interventions

Intervention 1: Intervention group: 4 educational sessions including: the day before Intervention , 24 hours after surgery (after leaving the bed), 48 hours after surgery, and then during discharge, u

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: 50-70 years old Men and women with osteoarthritis undergoing total knee replacement No affection to acute anxiety disorder, depression and psychological problems and not taking psychoactive drugs before and after surgery. (According to the patient's statements and the diagnosis of physical and mental health by referring to the patient's medical records) Having no history of joint replacement or surgery on the knee Having a BMI of less than 30 kg / m Having reading and writing skills (and in case of no literacy, one of the literate carers should be involved in the patient's education process)

Exclusion criteria

Exclusion criteria: Pre-surgery infection that affects the outcome of the research Failure to co-operate with the patient in exercising and training Patients unable to walk and unable to attend exercises There are some underlying problems in the patient that make it impossible to attend rehabilitation sessions such as: severe heart and respiratory disease

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: before & 6 weeks afterintervention. Method of measurement: Spielberg state anxiety questionnaire.;Pain, stiffness and physical function. Timepoint: before & 6 weeks afterintervention. Method of measurement: WOMAC questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBatoul Atabaki

Iran University of Medical Sciences

shryda.atabaki@yahoo.com+98 21 86701

Outcome results

None listed

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