Comparison between MSI and routine physiotherapy treatments in knee pain patients

Not Applicable

Recruiting

Conditions: G89.4
Condition 1: Knee pain. Condition 2: Chronic pain.
Pain in knee
Chronic pain syndrome
M25.56

Registration Number: IRCT20180627040251N5

Lead Sponsor: Kharazmi University

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 40

Inclusion Criteria

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

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.