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Pulsed electromagnetic fields in association with home exercise program in the management of patellofemoral pain syndrome.

Therapeutic efficacy of pulsed electromagnetic fields in association with home exercise program in the management of patellofemoral pain syndrome: a randomized controlled study at one year follow-up.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN74296451
Enrollment
31
Registered
2015-02-03
Start date
2010-05-01
Completion date
Unknown
Last updated
2015-07-06

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

Conditions

Patellofemoral pain syndrome is a common cause of knee pain in young adults, especially in females who practice sport activities. Musculoskeletal Diseases

Interventions

Patients affected by patellofemoral pain syndrome will be randomized: 1. Pulsed electromagnetic fields (I-ONE) therapy 4 hours/day for 60 days associated with home exercise program 2. Only home exerci

Sponsors

Federico II University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The presence of at least three of the following symptoms: pain when walking up or down stairs, pain when squatting, pain when running, pain when cycling, pain when sitting with knees flexed for a prolonged time, grinding of the patella, and a positive clinical patellar test (such as Clarke’s test or patellar femo-ral grinding test) 2. Untreated pain lasting for more than 3 months 3. Age between 15 and 45 years 4. Informed consent given

Exclusion criteria

Exclusion criteria: 1. Knee capsular ligament or meniscus tears 2. Previous knee surgery 3. Severe knee varus/valgus deformities (>10°) 4. Lower limbs prosthesis 5. Corticosteroid therapy 6. B.M.I. > 30 kg/m2 7. Infections 8. Rheumatoid arthritis and autoimmune diseases 9. Malignancy 10. Systemic diseases 11. Plateau-patella angle 30°

Design outcomes

Primary

MeasureTime frame
Function of the knee assessed by Victorian Institute of Sport Assessment score (VISA)

Secondary

MeasureTime frame
Pain reduction assessed by: 1. Visual analogue scale (VAS) 2. NSAIDs consumption

Countries

Italy

Outcome results

None listed

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