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Study on Magnetic Field Therapy to Improve Quality of Sleep and Reduction of Chronic Spine Pain

A Double-Blind, Randomized, Placebo-Controlled Study on Magnetic Field Therapy to Improve Quality of Sleep and Reduction of Chronic Spine Pain (Sleep/Mag)

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00445133
Acronym
SLEEP/MAG
Enrollment
80
Registered
2007-03-08
Start date
2007-02-28
Completion date
2007-12-31
Last updated
2007-09-27

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

Conditions

Back Pain, Neck Pain, Sleep Initiation and Maintenance Disorders

Keywords

Neck Pain/Lumbar pain/Magnets/sleep deficiency/ insomnia/

Brief summary

HYPTHOTHESIS: The researchers hypothesize that application of active magnetic therapy vs. sham utilized while individuals sleep can reduce neuropathic pain in the spine and improve the quality of sleep. The null hypothesis is that treatment of subjects with spine pain with exposure to permanent/static magnetic fields has no measurable effect on neuropathic pain scores or quality of sleep scores.

Detailed description

DESIGN: This is a double-blind, randomized, placebo-controlled study which will consist of two treatment groups. Treated subjects will receive a permanent/static magnetic sleeping pad with a nominal strength of less than 1000 Gauss. Control subjects will receive physically identical sleeping pad with a nominal surface field strength of 0 Gauss (placebo). The magnets will be contained in a standard mattress pad and subjects will sleep on the pad. The primary outcome measures will be quality of sleep as well as the daily VAS scores. These are subjective. There will be objective assessment by the quantification of autonomic nervous system (ANS) strengths of the parasympathetic and sympathetic effects from this non-invasive digital study using spectral analysis. Individuals will be evaluated at onset of study and at end of study to look at specifics of range of motion, spasm, radiculitis, etc. Scores will be kept on a monthly basis as well as repeat of ANS testing each month. At the end of the study, individuals will return all forms, be reevaluated by Dr. Weintraub and also will be asked questions regarding PGIC for bias, etc. Additionally heart rate and systolic and diastolic BP readings at rest and with challenge of standing will be recorded at baseline and each visit to determine if there is an anti-hypertensive effect from sleeping on magnetic device. A reduction of 3 mm Hg improves stroke and cardiac risk by a minimum of 4%. No new anti-hypertensive medications will be allowed.

Interventions

DEVICEMagnetic Sleep Pad

Sponsors

Weintraub, Michael I., MD, FACP, FAAN
Lead SponsorINDIV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Female or male subjects age 18-80. * Capable of understanding and complying with study protocols. * Chronic cervical, thoracic or lumbar pain for at least six months. * Sleep difficulties and/or insomnia

Exclusion criteria

* Unable to understand informed consent (mental retardation, psychosis, communicative impairment). * Cardiac pacemaker or other mechanical internal devices. * Tumor in the spine/history of malignancy. * Pregnancy. * Prior spine surgery

Design outcomes

Primary

MeasureTime frame
VAS Pain scores/Pittsburgh Sleep scores/Insomnia sleep scores/SF 15 pain descriptor scores/PGIC/

Secondary

MeasureTime frame
Autonomic Nerve Functions

Countries

United States

Contacts

Primary ContactMichael I. Weintraub, MD
miwneuro@pol.net914-941-0788
Backup ContactSusan E Wolert
miwneuro@pol.net914-941-0788

Outcome results

None listed

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