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Clinical Trial Summary

This study aims to test the efficacy of the ActiPatch® device by means of a randomized double blind controlled trial in a convenience sample of chronic low back pain patients at RPAH pain clinic. Outcome measures are validated psychometric measures evaluating known determinants of pain related disability, functional capacity measures, and pain scores; and a bespoke questionnaire assessing fidelity with recommended usage, and willingness to reduce analgesic or other pain related medications with the future assistance of the ActiPatch®.


Clinical Trial Description

This study aims to test the efficacy of the ActiPatch® device by means of a randomised double blind controlled trial in a convenience sample of chronic low back pain patients at Royal Prince Alfred Hospital (RPAH) pain clinic. Outcome measures are validated psychometric measures evaluating known determinants of pain related disability, functional capacity measures, and pain scores; and a bespoke questionnaire assessing fidelity with recommended usage, and willingness to reduce analgesic or other pain related medications with the future assistance of the ActiPatch®. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03828864
Study type Interventional
Source BioElectronics Corporation
Contact Graeme Campbell
Phone (02) 95159016
Email graeme.campbell1@health.nsw.gov.au
Status Not yet recruiting
Phase N/A
Start date February 1, 2019
Completion date May 1, 2020

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