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Magnetic Field Application in Patellofemoral Pain Syndrome

Investigating the Effect of Magnetic Field Application Used in Patellofemoral Pain Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06289400
Enrollment
30
Registered
2024-03-01
Start date
2024-03-01
Completion date
2024-10-24
Last updated
2024-12-04

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

Conditions

Pain, Knee

Keywords

Pain, Knee, Magnetic field, Physiotherapy

Brief summary

The purpose of this study is to examine the effect of magnetic field application used in the treatment of patellofemoral pain.

Detailed description

The aim of this randomized controlled study is to examine the effect of magnetic field application used in the treatment of patellofemoral pain. 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?

Interventions

DEVICEMagnetic 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.

OTHERConventional 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.

Sponsors

KTO Karatay University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Having been diagnosed with patellofemoral pain syndrome by an orthopedic physician * Volunteering to participate in the study * Having pain for more than eight weeks * Patients who did not undergo surgery

Exclusion criteria

* Patients diagnosed with rheumatological disease * 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

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scale (VAS)The evaluation will be applied at the beginning of the treatment program.A Visual Analogue Scale (VAS) is one of the pain rating scales.Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between no pain and worst pain.
36-Item Short Form Survey (SF-36)The evaluation will be applied at the beginning of the treatment program.The SF-36 is a 36-item self-report measure of health-related quality of life. It has eight subscales measuring different domains of health-related quality of life: physical functioning (PF), role-physical (RP), bodily pain (BP), general health (GH), vitality (VT), social functioning (SF), role-emotional (RE), and mental health (MH).
Manual Muscle TestThe evaluation will be applied at the beginning of the treatment program.Manual muscle testing is based on the physiotherapist manually applying resistance to the muscle or muscle group to be evaluated.
The Lower Extremity Functional Scale (LEFS)The evaluation will be applied at the beginning of the treatment program.The Lower Extremity Functional Scale (LEFS) is a questionnaire containing 20 questions about a person's ability to perform everyday tasks. The LEFS can be used by clinicians as a measure of patients' initial function, ongoing progress and outcome, as well as to set functional goals.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026