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the effect of subject specific Foot progression angle retraining in knee osteoarthritis.

the effect of subject specific Foot progression angle retraining on the kinetics, kinematic, muscle activation and functional ability during walking in patients with knee osteoarthritis.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20101017004952N8
Enrollment
36
Registered
2019-10-09
Start date
2019-10-23
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

knee osteoarthritis disease. Primary generalized (osteo)arthritis

Interventions

Intervention 1: Intervention group: gait retraining. Intervention 2: Intervention group:change the walking pattern(Toe in or Toe out) on the basis the first session assessment.

Sponsors

Tarbiat modares university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Definite OA Grade II & III as defined by the Kellgren-Lawrence scale in one knee or, if bilateral, being mild in one side BMI: Between 25 and 30 Ability to walk independently on an even surface without any assistive devices Minimum age 45 and maximum 65 years old

Exclusion criteria

Exclusion criteria: History of intra-articular injections over the past 6 months (such as hyaluronic acid, hydrocortisone and PRP) History of regular physical activity in the past 3 months (at least 2 or 3 times per week and at least half an hour each time History of musculoskeletal disorders and lower extremity joint injuries affecting balance Severe TI or TO (57/7 ± 5/7) Pes Planus (Flat foot) (rigid and flexible), Pes cavus (High arch) Any malalignment of lower extremity which is evident by observation (Varus angel > 5? and Valgus angel > 15?) History of knee and lower extremity surgery, severe muscle weakness in lower extremity, MMT lower than 3/5 History of neurological, vestibular, neuromuscular diseases (Diabetes and Neurapathy), chronic orthopedic disorders of the trunk and lower extremities (Rheumatoid Arthritis), visual impairments, inability to comprehend commands Osteoporosis Taking medications not prescribed by a Rheumatologist. Unwillingness to participate in the study for any reason

Design outcomes

Primary

MeasureTime frame
Knee adduction moment. Timepoint: before and after six-week retraining. Method of measurement: motion analysis system, nexus software.;Knee flexion moment. Timepoint: before and after six-week retraining. Method of measurement: motion analysis system, nexus software.;Muscle activation. Timepoint: before and after six-week retraining. Method of measurement: Electromyography.

Secondary

MeasureTime frame
Pain. Timepoint: before and after six-week retraining. Method of measurement: visual analog scale.;Quality of life. Timepoint: before and after six-week retraining. Method of measurement: SF-36 questionnaire and WOMAC.;Functional activity. Timepoint: before and after six-week retraining. Method of measurement: 8-walking test and Timed up and go test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGiti Torkaman

Tarbiat modares university

torkamang@yahoo.com+98 21 8288 4509

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 18, 2026