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

Phase 4

• Conditions: Back Pain; Neck Pain; Sleep Initiation and Maintenance Disorders

• Registration Number: NCT00445133
• Lead Sponsor: Weintraub, Michael I., MD, FACP, FAAN

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.

Study Timeline

• Study Start: 2007-02
• Study First Submitted: 2007-03-06
• Study First Submitted QC: 2007-03-07
• Study First Posted: 2007-03-08
• Status Verified: 2007-09
• Last Update Submitted: 2007-09-26
• Last Update Posted: 2007-09-27
• Study Completion: 2007-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 80

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
VAS Pain scores/Pittsburgh Sleep scores/Insomnia sleep scores/SF 15 pain descriptor scores/PGIC/

Secondary Outcome Measures

Name	Time	Method
Autonomic Nerve Functions

Trial Locations

Locations (1)

Dr. Michael I . Weintraub; 🇺🇸 Briarcliff Manor, New York, United States