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The effectiveness of PEMF in improving physical function among Osteoarthritic (OA) patients remains a topic of debate, leading to the American College of Rheumatology not yet endorsing its use in OA treatment. Therefore, it's essential to investigate PEMF therapy's efficacy in alleviating joint pain, stiffness, and enhancing physical function in knee OA patients Our study objectives were to evaluate the effectiveness and safety of PEMF therapy and to compare its efficacy with TENS in knee OA management.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1: Patients treated with transcutaneous electrical nerve stimulation (TENS) | Active Comparator |
| |
| Group 2: Patients treated with magnetotherapy (PEMF) | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| comparing efficacy of TENS and PEMF in knee osteoarthritis | Device | Sessions will be conducted by a physiotherapist from the center, trained in the technique.Three sessions per week for three weeks. We used an Automatic Program (approximately 20 minutes). For each group, the physical therapy was given as below: G2: Patients treated with magnetotherapy: -Device used: a prototype of a Health magnetic therapy (H.M.T) generator developed by a group of engineering researchers at the University of Tunis El Manar, employing low-frequency electromagnetic waves. The chosen program is "Analgesia". An applicator containing magnets will be placed on the affected knees. The patient will sit on a chair bending knees. G1 : Patients treated with TENS -Device used: TENS from ECO2 from Schwa Medico, 2016, France. We chose the "Gate control" program (high frequency). The patient will sit with bent knees on a chair and adhesive patches will be placed on the affected knee. The intensity will be adapted to the patient's tolerance in both groups. |
| Measure | Description | Time Frame |
|---|---|---|
| response to physical therapy | a 20 percent decrease in the total score of WOMAC pain | one week before the beginning and 3 weeks after the finishing of the rehabilitation program |
| Measure | Description | Time Frame |
|---|---|---|
| reduction of pain | Reduction in visual analog scale (VAS) pain scores at rest and during activity. | one week before the beginning and 3 weeks after the finishing of the rehabilitation program |
| Consumption of paracetamol |
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Inclusion Criteria:
We included patients who had knee pain due to knee OA diagnosed according to the American College of Rheumatology including:
Knee pain AND presence of at least three of the following 6 criteria:
Exclusion Criteria:
For both groups, we did not include:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Emna RAZGALLAH, medical resident | Contact | 25484674 | +216 | emna.razgallah123@gmail.com |
| Maroua SLOUMA, Medical doctor | Contact | 55117316 | +216 | maroua.slouma@gmail.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Military Hospital of Tunis | Recruiting | Tunis | 1008 | Tunisia |
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| ID | Term |
|---|---|
| D020370 | Osteoarthritis, Knee |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
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|
| one week before the beginning and 3 weeks after the finishing of the rehabilitation program |
| assessing safety | occurrence of adverse effects requiring temporary or permanent discontinuation of the technique. | one week before the beginning and 3 weeks after the finishing of the rehabilitation program |
| assessing patients satisfaction | Satisfaction VAS | one week before the beginning and 3 weeks after the finishing of the rehabilitation program |
| stiffness and function improvement | • Improvement in all three domains of WOMAC and overall WOMAC score: Stiffness (2 questions) and function (17 questions) WOMAC subscales | one week before the beginning and 3 weeks after the finishing of the rehabilitation program |
| D012216 |
| Rheumatic Diseases |