Effect of online rehabilitation intervention in home versus control group on the rehabilitation of patients after total knee arthroplasty

Effect of online rehabilitation intervention in home versus control group on the rehabilitation of patients after total knee arthroplasty: a randomized clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N558

Enrollment

Registered

2025-05-04

Start date

2025-05-15

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Total knee arthroplasty. Presence of artificial knee joint

Interventions

Intervention 1: Intervention group: Routine care after total knee arthroplasty plus online training of an exercise program 3 times a week for 2 weeks (including quadriceps sets, straight leg raises, a

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age 18 to 75 years Patient candidate for total knee arthroplasty Literacy Access to cyberspace and the Internet

Exclusion criteria

Exclusion criteria: Inability to perform sports exercises

Design outcomes

Primary

Measure	Time frame
Quality of life. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the SF-36 Quality of Life Questionnaire.;Mean score of pain. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the Visual Analog Scale (VAS).;Range of motion level. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: By clinical examination.;6-minute walk test score. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the 6-minute walk test.	—

Measure

Time frame

Quality of life. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the SF-36 Quality of Life Questionnaire.;Mean score of pain. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the Visual Analog Scale (VAS).;Range of motion level. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: By clinical examination.;6-minute walk test score. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the 6-minute walk test.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mobin Ahmadi Niaz

Hamedan University of Medical Sciences

ahmadimobin74@yahoo.com+98 81 3838 0572

Outcome results

None listed

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