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Effect of subtalar strap and high top shoes in medial knee compartment osteoarthritis

Assessment and comparison of the effects of lateral wedge insole with subtalar strap versus lateral wedge insole with high-top shoe on pain and function in patients with medial knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250405065209N1
Enrollment
32
Registered
2025-04-06
Start date
2025-04-07
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

Medial knee osteoarthritis. Osteoarthritis of knee

Interventions

Intervention 1: Intervention group 1:Lateral wedge insoles for these patients will be manufactured using CAD-CAM technology. Initially, a plantar pressure scan will be taken from the patient using a P

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to No maximum

Inclusion criteria

Inclusion criteria: The diagnosis of symptomatic unilateral MKOA will be made according to Kellgren-Lawrence classification grades I, II, or III WOMAC total score will be =31 out of 100 Moderate activity: at least 1 hour per week of sustained physical activity at any intensity, and 2 times per week. =2° of varus knee alignment in the affected limb. 2-mm radiographic medial joint space narrowing.

Exclusion criteria

Exclusion criteria: Advanced-stage knee osteoarthritis (grade IV according to the Kellgren-Lawrence classification). Any other inflammatory arthritis (rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis). Avascular necrosis of the knee joint. Injection (intra-articular or soft-tissue) in the affected knee in the past 2 months.

Design outcomes

Primary

MeasureTime frame
Pain score on the Visual Analog Scale. Timepoint: Before, immediately after, and four weeks after wearing the orthoses. Method of measurement: The Visual Analogue Scale (VAS) will be a 100 mm line on which individuals will be asked to mark their level of pain. The researcher will then measure the distance from the starting point to the marked point in centimeters.

Secondary

MeasureTime frame
Time of timed up and go test. Timepoint: Before, immediately after, and four weeks after wearing the orthoses. Method of measurement: The Timed Up and Go (TUG) test will involve asking the individual to stand up from a seated position, walk a predetermined distance of three meters at their chosen speed and stride length, turn around, and walk the distance again until they reach the chair and sit down. The time taken to complete this series of activities will be the criterion for evaluation, measured with a stopwatch with an accuracy of 0.01 seconds.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhossein Mofidi

University of social welfare and rehabilitation sciences

amirhosseinmofidito@gmail.com009822180010

Outcome results

None listed

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