Cereset Research Standard Operating Procedures for Insomnia: A Randomized, Controlled Clinical Trial

Author:

Tegeler Catherine L.1ORCID,Munger Clary Heidi1ORCID,Shaltout Hossam A.2ORCID,Simpson Sean L.3ORCID,Gerdes Lee4ORCID,Tegeler Charles H.1ORCID

Affiliation:

1. Department of Neurology, Wake Forest School of Medicine (WFSM), Winston-Salem, NC, USA

2. Hypertension and Vascular Research Center, WFSM, Winston-Salem, NC, USA

3. Department of Biostatistics and Data Sciences, WFSM, Winston-Salem, NC, USA

4. Brain State Technologies, LLC, Scottsdale, AZ, USA

Abstract

BackgroundInterventions for insomnia that also address autonomic dysfunction are needed.ObjectiveWe evaluate Cereset Research™ Standard Operating Procedures (CR-SOP) in a pilot randomized, controlled trial. CR-SOP is a less operator-dependent, more generalizable innovation of HIRREM®, a noninvasive, closed-loop, allostatic, acoustic stimulation neurotechnology demonstrated to improve insomnia and autonomic function.MethodsAdults with Insomnia Severity Index (ISI) scores of ≥8 were randomized to receive ten sessions of CR-SOP, with tones linked to brainwaves (LB, intervention), or a sham condition of random tones not linked to brainwaves (NL, control). Measures were collected at enrollment and 0-14 days and 4-6 weeks post-allocated intervention. The primary outcome was differential change in ISI from baseline to 4-6 weeks post-intervention. Secondary self-report measures assessed sleep quality65 and behavioral outcomes. Ten-minute recordings of heart rate and blood pressure were collected to analyze autonomic function (heart rate variability [HRV] and baroreflex sensitivity).ResultsOf 22 randomized, 20 participants completed the allocated condition. Intention to treat analysis of change from baseline to the 4-6 week outcome demonstrated mean ISI score reduction of 4.69 points among controls (SE 1.40). In the intervention group, there was an additional 2.58 point reduction in ISI score (SE 2.13; total reduction of 7.27, P = .24). Sleep quality and some measures of autonomic function improved significantly among the intervention group compared to control.ConclusionsThis pilot study compared use of a standardized, allostatic, acoustic neurotechnology intervention with a sham, active control condition. The magnitude of change in insomnia severity was clinically relevant and similar to the findings in a prior, fully powered trial, but the differential improvement observed was not statistically significant. Significant improvements were demonstrated in sleep quality and some autonomic function measures.

Funder

The Susanne Marcus Collins Foundation, Inc

Wake Forest Clinical and Translational Science Institute

REDCap infrastructure for data collection and management

Publisher

SAGE Publications

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