Evaluating The Effect of Using Two density Insoles with Lateral Wedge in the Elderly with Medial Compartment Knee Osteoarthritis

Evaluating The immediate Effect of Using Two density Insoles with Lateral Wedge Embedded inside a Novel Neoprene Sock on Pain, Quality of Life, and Biomechanical Parameters of the Knee Joint During walking in the Elderly with Medial Compartment Knee Osteoarthritis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230528058315N1

Enrollment

Registered

2023-08-12

Start date

2023-08-23

Completion date

Unknown

Last updated

2023-08-21

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

Conditions

osteoarthritis of the medial compartment of the knee joint. Unspecified osteoarthritis, unspecified site

Interventions

A pair of laced neoprene socks equipped with medical insoles will be provided to people with one-sided osteoarthritis of the internal compartment of the knee joint. The neoprene sock encompasses a med

Eligibility

Sex/Gender

All

Age

60 Years to 75 Years

Inclusion criteria

Inclusion criteria: unilateral osteoarthritis of the medial compartment of the knee joint

Exclusion criteria

Exclusion criteria: Any symptom caused due to the negative effect of the intervention receiving any simultaneous treatment in the form of intra-articular injection or physical therapy the presence of any accompanying injury such as problems in the wrist and hip joints low back pain rheumatoid arthritis

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: before and immediately after intervention. Method of measurement: visual analogue scale.;Quality of life. Timepoint: before and immediately after intervention. Method of measurement: Persian version of S-F36 questionnaire.;Spatiotemporal parameters of walking. Timepoint: before and immediately after intervention. Method of measurement: Qualysis motion capture system.;Ground Reaction Force. Timepoint: before and immediately after intervention. Method of measurement: Kistler Force platform.	—

Measure

Time frame

Pain. Timepoint: before and immediately after intervention. Method of measurement: visual analogue scale.;Quality of life. Timepoint: before and immediately after intervention. Method of measurement: Persian version of S-F36 questionnaire.;Spatiotemporal parameters of walking. Timepoint: before and immediately after intervention. Method of measurement: Qualysis motion capture system.;Ground Reaction Force. Timepoint: before and immediately after intervention. Method of measurement: Kistler Force platform.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Tafti

Hamedan University of Medical Sciences

N.Tafti@umsha.ac.ir+98 81 3838 1633

Outcome results

None listed

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