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Comparison between EMG-Biofeedback controlled exercises and conventional exercises on knee osteoarthritis treatment, a clinical trial.

Clinical trial of comparison between effect of EMG-Biofeedback controlled exercises and effect of conventional exercises on knee osteoarthritis treatment.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015101024451N1
Enrollment
50
Registered
2015-11-22
Start date
2015-10-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Knee osteoarthritis. Gonarthrosis [arthrosis of knee]

Interventions

1-Received ten sessions of EMG-Biofeedback controlled knee osteoarthritis exercises.These exercises include: Strengthening exercises of Quadriceps muscles, Strengthening of Hip adductors, Closed Kinem
TENS(by CM mode,for twenty minutes on path of pain, HP(,for twenty minutes) and US( pulse method, one MHz frequency for five minutes0. Intervention 2: Control group
1-Conventional knee osteoarthritis exercises training to patients include
Strengthening exercises of Quadriceps muscles, Strengthening of Hip adductors, Closed Kinematic Chain exercises, Stretching exercises for Hamstring muscle and Properioception training by physical ther
TENS(by CM mode,for twenty minutes on path of pain, HP(,for twenty minutes) and US( pulse method, one MHz frequency for five minutes.
Rehabilitation
Intervention group
Control group

Sponsors

Vice Chancellor for research of Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Knee osteoarthritis according to criteria of American College of Rheumatology(ACR); Knee pain at least for 6 months; Absence of inflammatory joint disease or secondary osteoarthritis; No physical treatments program in the previous year; No intraarticular injections at the last three months; No history of knee surgery; Exclusion criteria; The tendency of patient to withdraw from the project at any time.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before intervention, one month after intervention, two months after intervention. Method of measurement: VAS (Visual Analogue Scale).;Symptoms and quality of life. Timepoint: Before intervention, one month after intervention, two months after intervention. Method of measurement: KOOS (Knee Injury and Osteoarthritis Outcome Score) questionnaire.

Secondary

MeasureTime frame
Vastus Medialis to Vastus Lateralis muscles mean force ratio. Timepoint: Before intervention , one month after intervention, two months after intervention. Method of measurement: by electromyography device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Yahyaei Bavil

Department of Physical Medicine and Rehabilitation, Iran University of medical sciences

yahyaei89@gmail.com+98 21 8214 1229

Outcome results

None listed

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