Magnetic Field Application in Patellofemoral Pain Syndrome
NCT ID: NCT06289400
Last Updated: 2024-12-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2024-03-01
2024-10-24
Brief Summary
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Detailed Description
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The main question it aims to answer is;
Is magnetic field therapy applied in addition to conventional treatment effective in reducing pain in individuals with Patellofemoral pain syndrome?
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Study Group
Conventional treatment+ Magnetic field application
Magnetic field application
The applicator (Size: 15x15 cm) has placed 1-3 cm above the skin surface at the painful area. During the treatment, treatment has applied with ready-made protocols included in the device.
Conventional treatment
Within the scope of conventional treatment, hotpack application, transcutaneous electrical stimulation (TENS), interferential current and ultrasound treatment modalities will be applied. In addition, strengthening exercises will be applied to the muscles around the hip and knee and stretching exercises will be applied to the short muscle groups.
Control Group
Conventional treatment
Conventional treatment
Within the scope of conventional treatment, hotpack application, transcutaneous electrical stimulation (TENS), interferential current and ultrasound treatment modalities will be applied. In addition, strengthening exercises will be applied to the muscles around the hip and knee and stretching exercises will be applied to the short muscle groups.
Interventions
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Magnetic field application
The applicator (Size: 15x15 cm) has placed 1-3 cm above the skin surface at the painful area. During the treatment, treatment has applied with ready-made protocols included in the device.
Conventional treatment
Within the scope of conventional treatment, hotpack application, transcutaneous electrical stimulation (TENS), interferential current and ultrasound treatment modalities will be applied. In addition, strengthening exercises will be applied to the muscles around the hip and knee and stretching exercises will be applied to the short muscle groups.
Eligibility Criteria
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Inclusion Criteria
* Volunteering to participate in the study
* Having pain for more than eight weeks
* Patients who did not undergo surgery
Exclusion Criteria
* Patients who have previously had steroid injections in the knee area
* Patients with entrapment neuropathy and deformity in the lower extremity
* Patients who are pregnant
* Patients suffering from scoliosis,
* Patients who use non-steroidal anti-inflammatory and antidepressant regularly for any reason
18 Years
65 Years
ALL
No
Sponsors
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KTO Karatay University
OTHER
Responsible Party
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Principal Investigators
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Osman Karaca, PhD
Role: STUDY_CHAIR
KTO Karatay University
Locations
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KTO Karatay University
Konya, , Turkey (Türkiye)
Countries
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Other Identifiers
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KaratayUOAS
Identifier Type: -
Identifier Source: org_study_id