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Electromagnetic Field Therapy
Acute/subacute; active device for Lower Back Pain
N/A
Waitlist Available
Research Sponsored by University of Bridgeport
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, weeks 6 and 12
Awards & highlights
Study Summary
This study will examine the effects of a portable of pulsed electromagnetic field (PEMF) device (MD Cure, Aerotel, USA) compared with a sham device on patient-reported outcomes of pain and function in patients with either acute/subacute or chronic low back pain (LBP).
Eligible Conditions
- Lower Back Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, weeks 6 and 12
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, weeks 6 and 12
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in low back pain related disability
Change in pain intensity
Trial Design
4Treatment groups
Experimental Treatment
Placebo Group
Group I: Chronic; active deviceExperimental Treatment1 Intervention
MDCure active device
Group II: Acute/subacute; active deviceExperimental Treatment1 Intervention
MDCure active device
Group III: Acute/subacute; shamPlacebo Group1 Intervention
MDCure sham device
Group IV: Chronic; shamPlacebo Group1 Intervention
MDCure sham device
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Who is running the clinical trial?
University of BridgeportLead Sponsor
2 Previous Clinical Trials
252 Total Patients Enrolled
Frequently Asked Questions
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