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BEMER in the Treatment of Pain in Fibromyalgia.

Not Applicable
Completed
Conditions
Fibromyalgia
Interventions
Device: BEMER electromagnetic field therapy
Registration Number
NCT02310386
Lead Sponsor
Central Finland Hospital District
Brief Summary

Fibromyalgia is one the most common causes of chronic pain syndromes in women. It causes considerable costs in primary health care setting as well as specialized medical care sector.Electrotherapy and exercise therapy has shown to have short-term pain relieving effects in randomized controlled trials (RCT) among fibromyalgia patients. However, there is sparse knowledge about the effects of long-term RCTs in the treatment of pain in fibromyalgia, as there are no publications about cost-effectiveness analysis of such treatments.

The aim of this study is to investigate whether the BEMER electromagnetic field therapy device has beneficial long-term effects in the treatment of pain, and whether it improves fibromyalgia patients' quality of life. In addition, this study investigates whether the BEMER device treatment is cost-effective in the treatment of fibromyalgia patients.

Detailed Description

The participants of this study are working age female patients from the Central Finland Health Care District, and who have been treating because of severe pain. After eligibility has been assessed by health-related questionnaire and clinical examination, the participants will be randomly assigned into the treatment or control group. Treatment group patients will receive the loan activated BEMER-care unit, while controls will receive inactivated sham BEMER-unit. All participants will use the device regularly on a daily bases over three months. After one month treatment break, the treatment group will become a control group and control group will become a treatment group according cross-over design principle. Switching the groups will take place by changing the BEMER devices during the break. Throughout the study, both participants and researchers are unaware whether the participants are using activated or inactivated BEMER-devices. The research will be carried out and coordinated by Central Finland Central Hospital, and the research project will take place between September 2014 and June 2018.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
110
Inclusion Criteria
  • diagnosis of fibromyalgia
  • chronic persistent moderate or severe pain for more than 12 months
  • average minimum pain intensity of 5 in the scale of 0 to 10 during the last 7 days
  • age between 18 and 60 years
  • female gender
Exclusion Criteria
  • an inflammatory rheumatic disease
  • some other chronic pain disease as fibromyalgia
  • psychiatric illness
  • addiction to opiates
  • substance abuse
  • smoking
  • a person with disability
  • pregnancy and breast-feeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
activated BEMER-deviceBEMER electromagnetic field therapyActivated BEMER electromagnetic field therapy (BEMER, Innomed International, AG, Lichtenstein).
inactivated BEMER-deviceBEMER electromagnetic field therapyInactivated BEMER electromagnetic field therapy (BEMER, Innomed International, AG, Lichtenstein).
Primary Outcome Measures
NameTimeMethod
Pain and stiffnessChange from Baseline Pain and Stiffness at 3 months

Visual Analogue Scale (VAS)

Secondary Outcome Measures
NameTimeMethod
Cost-effectivenessThree Months Before and After the Start of the Intervention

Questions about the use of drugs, visit to doctors, physiotherapy visits, and other health-care visits.

Severity of depressionChange from Baseline Severity of Depression at 3 Months

Depression Scale (DEPS)

Quality of lifeChange from Baseline Quality of Life at 3 month

RAND-36 Questionnaire

Symptoms and functional abilityChange from Baseline Symptoms and Functional Ability at 3 months

Fibromyalgia Impact Questionnaire (FIQ)

Trial Locations

Locations (1)

Jyväskylä Central Hospital

🇫🇮

Jyväskylä, Central Finland, Finland

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