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Very Low Frequency Magnetic Fields in the Treatment of Fibromyalgia

Effectiveness of Very Low Frequency Magnetic Fields in the Treatment of Fibromyalgia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02231541
Enrollment
37
Registered
2014-09-04
Start date
2014-09-30
Completion date
2015-03-31
Last updated
2015-06-08

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

Conditions

Fibromyalgia

Keywords

Fibromylgia, Magnetic Fields, Pain, Visual Analogue scale

Brief summary

The purpose of the study is to determine the effectiveness of treatment with very low frequency electromagnetic fields on the reduction of pain in patients with fibromylgia, disease presenting with widespread musculoskeletal pain usually associated with other symptoms such as stiffness, fatigue, sleep disturbances, depression, anxiety.

Interventions

DEVICEVery Low Frequency Magnetic Fields

The device is set to an analgesic program lasting about 30 minutes.

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Fibromyalgia diagnosed according to the criteria proposed by the American College of Rheumatology (ACR 2010) * Subjects aged between 18 and 60 years

Exclusion criteria

* Pregnant patients * Patients with pacemaker or other metal implants * Systemic infectious disorders * Neoplastic disorders * Epilepsy * Severe heart disease

Design outcomes

Primary

MeasureTime frameDescription
Change of Visual Analogue Scale (VAS) from baseline to 12 weeksbaseline, 4 weeks, 12 weeksIt is a scale for the assessment of pain and it's based on a ten point scale, where 0 means no pain and 10 the greatest pain ever both at rest and during movements.

Secondary

MeasureTime frameDescription
Change of Fibromylgia Impact Questionnaire (FIQ) from baseline to 12 weeksbaseline, 4 weeks, 12 weeksThe questionnaire assesses disability and symptoms. It is divided into ten sub-categories that assess the range of symptoms presented by the patient and the response to therapy and structured in twenty questions that assess disability in activities of daily living (ADL), the difficulties in practice, the feeling of general well-being, sleep, severity of symptoms, including pain, fatigue, depression, anxiety and rigidity. The questionnaire is self-administered disease-specific, and each item is based on a metric scale ranging from 0 (no disability) to 10 (maximum disability).
Change of Fibromylgia Assessment Status (FAS) from baseline to 12 weeksbaseline, 4 weeks, 12 weeksThe questionnaire assesses the response to therapy and the progression of the disease. Specifically it evaluates fatigue, sleep disorders and pain. The questionnaire is disease-specific, self-administered and is constituted by a pain map, called Self-Assessment Pain Scale (SAPS) characterized by a metric scale from 0 to 3 and by two numerical scales for the assessment of fatigue and sleep quality, each characterized by a metric scale between 0 and 106.
Change of Health Assessment Questionnaire (HAQ) from baseline to 12 weeksbaseline, 4 weeks, 12 weeksThis questionnaire assesses disability. It is divided into eight domains that assess the dressing, eating, getting up, walking, hygiene, activities of achievement and activities of daily life. The questionnaire is self-administered and each item is based on a metric scale ranging from 0 (no disability) to 3 (maximum disability).

Countries

Italy

Outcome results

None listed

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