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Comparison between MSI and routine physiotherapy treatments in knee pain patients

The comparison of treatment using Movement System Impairment method with routine physical therapy in improving pain and function in patents with knee pain: A randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180627040251N5
Enrollment
40
Registered
2023-03-30
Start date
2023-03-28
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Condition 1: Knee pain. Condition 2: Chronic pain. Pain in knee Chronic pain syndrome

Interventions

Intervention 1: Intervention group: This group consists of patients with knee pain that are treatable with physiotherapy after initial assessment. In this group, patients are classified based on “Move

Sponsors

Kharazmi University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Knee pain at least 2 months before examination Pain between 30-70 based on "Numeral Rating Scale"

Exclusion criteria

Exclusion criteria: The confirmation of the need for surgery Systematic, Metabolic or Neurologic disease (such as radiculopathy) Pregnancy The need for analgesic or anti-inflammatory drugs during the treatment period

Design outcomes

Primary

MeasureTime frame
1) Pain score based on Numeral Rating Scale of 0-100. 100 shows the worst pain and 0 is the least amount of pain. Timepoint: At the start of the study (Before intervention) and 6 weeks after the start of the study (End of study). Method of measurement: Pain is evaluated by marking on a line which is divided to 100 points.

Secondary

MeasureTime frame
Knee alignment. Timepoint: At the start of the study (Before intervention) and 6 weeks after the start of the study (End of study). Method of measurement: Knee alignment is measured in standing, sitting, walking, standing on one leg, and stairs position.;Function based on questionnaire of Knee injury and Osteoarthritis Outcome Score. The score is a percentage score from 0 to 100, 0 representing extreme problems and 100 representing no problems. Timepoint: At the start of the study (Before intervention) and 6 weeks after the start of the study (End of study). Method of measurement: The function is measured by Knee injury and Osteoarthritis Outcome Score questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Hassan Sadeghi

Kharazmi University

Hassan.sadeghi81@yahoo.com+98 21 2222 8001

Outcome results

None listed

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