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Movement System Impairment classification approach at knee pain

The effect of movement system impairment-based classification treatment compared to routine physiotherapy on pain, disability, and alignment and movement impairments in individuals with tibiofemoral rotation syndrome: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210505051181N3
Enrollment
40
Registered
2022-05-28
Start date
2022-06-22
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Condition 1: Knee osteoarthritis. Condition 2: Patellofemoral pain.

Interventions

Intervention 1: Intervention group: Movement System Impairment based treatment. Intervention 2: Active control group: routine physiotherapy treatment.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: age between 18 and 40 years history of sudden or gradual pain at the knee complex or surrounding tissues a pain intensity of at least 3 points measured using a 0- to 10-point visual analog scale Pain during activities that include loading on a flexed knee; Such as: running, jumping, squatting, climbing and descending stairs Literacy for reading and writing Ability to understand Persian language

Exclusion criteria

Exclusion criteria: Musculoskeletal injuries other than patellofemoral pain; such as: meniscus injury, ligamentous injury, history of patellar dislocation, severe osteoporosis, progressive neurological disorders, lumbosacral radiculopathies History of any traumatic injury in the last 6 months History of any lower limb surgery in the last 6 months Any specific deformity in the spine and lower extremities; such as: scoliosis, kyphosis, femoral anteversion, tibial torsion Complaints of pain in the other joints of the lower limbs Constant severe pain that interferes with the testing process Taking the analgesic and anti-inflammatory drugs during the study The history of malignancy, cardiovascular disease Pregnancy

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: over the previous 24 hours and 1 week ago and immediately after the intervention. Method of measurement: Visual Analog Scale.;Disability. Timepoint: Before and immediately after the intervention. Method of measurement: Kujala Questionnaire.

Secondary

MeasureTime frame
Alignment and movement impairments. Timepoint: Before and immediately after the intervention. Method of measurement: alignment and movement impairments data form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyedeh Forouzan Mousavi

Iran University of Medical Sciences

mousavi.forouzan1995@gmail.com+98 21 2222 7124

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026