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Clinical effectiveness of active Alpha-Stim AID versus sham Alpha-Stim AID in major depression in primary care in England (Alpha-Stim-D): a multicentre, parallel group, double-blind, randomised controlled trial

Morriss, Richard; Patel, Shireen; Boutry, Clement; Patel, Priya; Guo, Boliang; Briley, Paul M.; Butler, Deborah; Craven, Michael; Duncan, Ashley; Griffiths, Christopher; Higton, Fred; McNaughton, Rebecca; Nixon, Neil; Prasad, Vibhore; Sayal, Kapil; Smart, David; Zafar, Azhar; Kai, Joe

Clinical effectiveness of active Alpha-Stim AID versus sham Alpha-Stim AID in major depression in primary care in England (Alpha-Stim-D): a multicentre, parallel group, double-blind, randomised controlled trial Thumbnail


Authors

RICHARD MORRISS richard.morriss@nottingham.ac.uk
Professor of Psychiatry and Community Mental Health

CLEM BOUTRY CLEM.BOUTRY@NOTTINGHAM.AC.UK
Research Associate

PRIYA PATEL Priya.Patel1@nottingham.ac.uk
Research Assistant

BOLIANG GUO BOLIANG.GUO@NOTTINGHAM.AC.UK
Associate Professor

PAUL BRILEY Paul.Briley3@nottingham.ac.uk
Clinical Assistant Professor in General Adult Psychiatry

Deborah Butler

Ashley Duncan

Christopher Griffiths

Fred Higton

Rebecca McNaughton

NEIL NIXON Neil.Nixon@nottingham.ac.uk
Clinical Associate Professor in Adult Mood Disorder

Vibhore Prasad

KAPIL SAYAL kapil.sayal@nottingham.ac.uk
Professor of Child and Adolescent Psychiatry

David Smart

Azhar Zafar



Abstract

Background: Randomised sham-controlled trials of cranial electrostimulation with the Alpha-Stim Anxiety Insomnia and Depression (AID) device have reported improved anxiety and depression symptoms; however, no adequately powered sham-controlled trials in major depression are available. We investigated whether active Alpha-Stim AID is superior to sham Alpha-Stim AID in terms of clinical effectiveness for depression symptoms in major depression. Methods: The Alpha-Stim-D trial was a multicentre, parallel group, double-blind, randomised controlled trial, recruiting participants from 25 primary care centres in two regions in England, UK. Eligible participants were aged 16 years or older with a current diagnosis of primary major depression, a score of 10–19 on the nine-item Patient Health Questionnaire, and had been offered or prescribed and reported taking antidepressant medication for at least 6 weeks in the previous 3 months. Main exclusion criteria were contraindications to Alpha-Stim AID device use, having persistent suicidal ideation or self-harm, neurological conditions, a substance use disorder or dependence, an eating disorder, bipolar disorder, or non-affective psychosis, or receiving psychological treatment in the past 3 months. Eligible participants were randomly assigned (1:1, minimised by region, anxiety disorder, and antidepressant use) to 1 h daily use of active (100 μA) or sham Alpha-Stim AID treatment for 8 weeks. Randomisation was via an independent web-based system, with participants, outcome assessors, and data analyst masked to treatment assignment. The primary outcome was change from baseline in score on the 17-item Hamilton Depression Rating Scale (HDRS-17, GRID version) at 16 weeks after randomisation, with participants analysed by intention to treat (ITT; all randomly assigned participants). Safety was assessed in all randomly assigned participants. The trial is registered with the ISRCTN registry (ISRCTN11853110); status completed. Findings: Between Sept 8, 2020, and Jan 14, 2022, 236 eligible participants were randomly assigned to active or sham Alpha-Stim AID (n=118 each). 156 (66%) participants were women, 77 (33%) were men, and three (1%) self-reported as other gender; 200 (85%) were White British or Irish; and the mean age was 38·0 years (SD 15·3; range 16–83). 102 (86%) participants in the active Alpha-Stim AID group and 98 (83%) in the sham group were followed up 16 weeks after randomisation. In the ITT population, mean change in GRID-HDRS-17 at 16 weeks was –5·9 (95% CI –7·1 to –4·8) in the active Alpha-Stim AID group and –6·5 (–7·7 to –5·4) in the sham group (mean change difference –0·6 [95% CI –1·0 to 2·2], p=0·46). Among the 236 participants, 17 adverse events were reported in 17 (7%) participants (nine [8%] participants in the active Alpha-Stim AID group; and eight [7%] participants in the sham group). One serious adverse event of suicidal ideation leading to hospitalisation was reported in the sham group, which was judged to be unrelated to the device. Interpretation: Active Alpha-Stim AID was safe and acceptable, but no more clinically effective than sham Alpha-Stim AID in major depression. Funding: National Institute for Health Research Applied Research Collaboration East Midlands and Electromedical Products International.

Citation

Morriss, R., Patel, S., Boutry, C., Patel, P., Guo, B., Briley, P. M., …Kai, J. (2023). Clinical effectiveness of active Alpha-Stim AID versus sham Alpha-Stim AID in major depression in primary care in England (Alpha-Stim-D): a multicentre, parallel group, double-blind, randomised controlled trial. Lancet Psychiatry, 10(3), 172-183. https://doi.org/10.1016/S2215-0366%2823%2900007-X

Journal Article Type Article
Acceptance Date Jan 27, 2023
Online Publication Date Jan 29, 2023
Publication Date 2023-03
Deposit Date Feb 20, 2023
Publicly Available Date Feb 20, 2023
Journal Lancet Psychiatry
Electronic ISSN 2215-0374
Publisher Elsevier BV
Peer Reviewed Peer Reviewed
Volume 10
Issue 3
Pages 172-183
DOI https://doi.org/10.1016/S2215-0366%2823%2900007-X
Keywords Biological Psychiatry; Psychiatry and Mental health
Public URL https://nottingham-repository.worktribe.com/output/16802599
Publisher URL https://www.sciencedirect.com/science/article/pii/S221503662300007X
Additional Information This article is maintained by: Elsevier; Article Title: Clinical effectiveness of active Alpha-Stim AID versus sham Alpha-Stim AID in major depression in primary care in England (Alpha-Stim-D): a multicentre, parallel group, double-blind, randomised controlled trial; Journal Title: The Lancet Psychiatry; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/S2215-0366(23)00007-X; CrossRef DOI link to the associated document: https://doi.org/10.1016/S2215-0366(23)00028-7; Content Type: article; Copyright: © 2023 The Author(s). Published by Elsevier Ltd.