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Effect of educational program on pain intensity and range of motion in patients undergoing joint replacement

Effect of mixed educational program on pain intensity and range of motion in patients undergoing hip and knee joint replacement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014111619980N1
Enrollment
64
Registered
2015-01-09
Start date
2015-01-13
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 and hip joint replacement. Presence of orthopaedic joint implants

Interventions

Intervention 1: Intervention group: The patient in addition to the usual treatments will receive the training sessions for 30 minutes which includes 20 minutes face to face training and 10 minutes qu
Rehabilitation
Intervention group: The patient in addition to the usual treatments will receive the training sessions for 30 minutes which includes 20 minutes face to face training and 10 minutes questions and answ
Control group: just received their usual treatment

Sponsors

Vice Chancellor for Research of Ahvaz Jundishapor University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The inclusion criteria : ability to understand Persian language; 18 years and older; elective surgery; no history of mental illness and addiction to opioids; lack of sensitivity to non steroidal anti-inflammatory drugs and analgesics. The exclusion criteria : the patient do not want to continue cooperating on the project; postoperative complications that affect the patients motor function.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: second day, third day, fourth day, fifth day and one month after intervention. Method of measurement: Numerical scale vas.;Range of motion. Timepoint: Discharge time, two weeks and one month later. Method of measurement: Goniometer.

Secondary

MeasureTime frame
Hip motor function. Timepoint: Before surgery, one month and three months after surgery. Method of measurement: Womac score(hip) questionnaire.;Knee motor function. Timepoint: Before surgery, one month and three months after surgery. Method of measurement: Womac score(knee) questionnaire.;Quality of life. Timepoint: Preoperatively and 3 months postoperatively. Method of measurement: Short 12-question questionnaire quality of life.;Anxiety. Timepoint: Before the intervention, and preoperative. Method of measurement: Spielberger scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Amirmohseni

Ahvaz Jundishapor University of Medical Sciences

amirmohseni.l@ajums.ac.ir+98 61 3377 7966

Outcome results

None listed

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