A Pilot Study Of The Effects Of Microcurrent On Three Sleep Surveys

Status Completed

Clinical Trial Summary

Participants identified as having primary insomnia will be randomly assigned to groups receiving microcurrent stimulation or sham in a double-blind randomized controlled trial. The microcurrent device used is FDA approved for the treatment of insomnia.

The hypothesis is that the experimental group will have significantly improved scores on three sleep surveys after treatment while the sham group will not.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

Primary Insomnia

Clinical Trial Details

NCT number	NCT00520832
Study type	Interventional
Source	Logan College of Chiropractic
Contact
Status	Completed
Phase	Phase 2
Start date	September 2007
Completion date	December 2007

View Details

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