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The effect of continues and every another day physical therapy on pain and function in subjects with knee osteoarthritis.

Evaluation of the effect of continues and intermittent physical therapy on amount of pain and function in subjects with moderate knee osteoarthritis (pilot randomized clinical trial)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171017036837N1
Enrollment
30
Registered
2018-09-18
Start date
2018-08-22
Completion date
Unknown
Last updated
2018-10-11

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

Conditions

Osteoarthritis. Osteoarthritis of knee, unspecified

Interventions

Intervention 1: Intervention group: 3 times a week, for 10 sessions every another day will be done. Conventional physiotherapy treatment includes these: 1. Transcutaneous electrical nerve stimulation(

Sponsors

Vice Chancellery of Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with primary knee osteoarthritis Having criteria of knee osteoarthritis according to American college of rheumatology Patients with grade 2 or 3 Kellgren-lawrence scale of moderate knee osteoarthritis Age more than 40 years Not being in the acute phase of the disease Able to write and read Men and women with moderate knee osteoarthritis Body mass index less than 35

Exclusion criteria

Exclusion criteria: Systemic rheumatoid arthritis Secondary knee osteoarthritis Active knee synovitis Severe knee trauma Surgery intervention on knee during 1 year ago Intra-articular injection of corticosteroids or hyaluronic acid for at least the last 6 months Performing a physiotherapy treatment in the last 3 months Taking of Non steroidal anti-inflammatory drug from a week before entering the study Musculoskeletal disorders in lower extrimities Disorders in lumbopelvic and hip region Bilateral involvement of knees which one of them is grade 4 Kellgren-lawrence scale

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: One day before the intervention and at the tenth session after the end of the treatment plan. Method of measurement: Visual Analogue Scale.;Function. Timepoint: One day before the intervention and at the tenth session after the end of the treatment plan. Method of measurement: Get up and go test.;Pain. Timepoint: One day before the intervention and at the tenth session after the end of the treatment plan. Method of measurement: Knee injury and osteoarthritis outcome score.;Pain. Timepoint: One day before the intervention and at the tenth session after the end of the treatment plan. Method of measurement: Intermittent and constant osteoarthritis pain.;Function. Timepoint: One day before the intervention and at the tenth session after the end of the treatment plan. Method of measurement: Six minute walk test.;Function. Timepoint: One day before the intervention and at the tenth session after the end of the treatment plan. Method of measurement: Knee injury and osteoarthritis outcome score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSayed Mohsen Mirbod

Esfahan University of Medical Sciences

mirbod@rehab.mui.ac.ir+98 31 3669 3089

Outcome results

None listed

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