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The Resource The effectiveness and risks of cranial electrical stimulation for the treatment of pain, depression, anxiety, PTSD, and insomnia : a systematic review, principal investigator, Paul Shekelle, Ian Cook; research associates, Isomi M Miake-Lye, Selene Mak, Marika Suttorp Booth, Roberta Shanman, Jessica M Beroes

The effectiveness and risks of cranial electrical stimulation for the treatment of pain, depression, anxiety, PTSD, and insomnia : a systematic review, principal investigator, Paul Shekelle, Ian Cook; research associates, Isomi M Miake-Lye, Selene Mak, Marika Suttorp Booth, Roberta Shanman, Jessica M Beroes

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Author
Contributor
Summary
Cranial electrical stimulation (CES) is a non-invasive method of applying low-intensity electrical current to the head. It is related to but distinct from other forms of transcranial electrical stimulation including electroconvulsive therapy, transcranial direct current stimulation (tDCS), and high-definition transcranial direct current stimulation. The different versions of transcranial electrical stimulation vary in the placement of electrodes, the intensity of the current, and the waveform of the current. According to Guleyupoglu and colleagues, CES evolved from the concept of "electrosleep," first investigated at the beginning of the 20th century. Most of the early research and applications occurred in Russia. Beginning in the 1960s, the concept of electrosleep became more popular in the USA. Because of the belief that the treatment did not actually induce sleep, but rather the sleep was a side effect of the relaxing effect of the current stimulation, the name was changed from "electrosleep" to "cranial electrical stimulation." Other proposed names, which have not persisted, included "transcerebral electrotherapy" and "NeuroElectric Therapy." The latter is noteworthy because it gave its name to an early CES device, the Neurotone 101, which was the first device approved by the FDA. All subsequent CES devices have been cleared for marketing by FDA based on the concept of claiming equivalency to the Neurotone 101. The status of cranial electrical stimulation devices and FDA regulation remains a matter of some controversy
Language
eng
Work
Publication
Extent
1 online resource (1 PDF file (50 pages))
Instance
Label
The effectiveness and risks of cranial electrical stimulation for the treatment of pain, depression, anxiety, PTSD, and insomnia : a systematic review
Title
The effectiveness and risks of cranial electrical stimulation for the treatment of pain, depression, anxiety, PTSD, and insomnia
Title remainder
a systematic review
Statement of responsibility
principal investigator, Paul Shekelle, Ian Cook; research associates, Isomi M Miake-Lye, Selene Mak, Marika Suttorp Booth, Roberta Shanman, Jessica M Beroes
Creator
Contributor
Author
Issuing body
Subject
Genre
Language
eng
Summary
Cranial electrical stimulation (CES) is a non-invasive method of applying low-intensity electrical current to the head. It is related to but distinct from other forms of transcranial electrical stimulation including electroconvulsive therapy, transcranial direct current stimulation (tDCS), and high-definition transcranial direct current stimulation. The different versions of transcranial electrical stimulation vary in the placement of electrodes, the intensity of the current, and the waveform of the current. According to Guleyupoglu and colleagues, CES evolved from the concept of "electrosleep," first investigated at the beginning of the 20th century. Most of the early research and applications occurred in Russia. Beginning in the 1960s, the concept of electrosleep became more popular in the USA. Because of the belief that the treatment did not actually induce sleep, but rather the sleep was a side effect of the relaxing effect of the current stimulation, the name was changed from "electrosleep" to "cranial electrical stimulation." Other proposed names, which have not persisted, included "transcerebral electrotherapy" and "NeuroElectric Therapy." The latter is noteworthy because it gave its name to an early CES device, the Neurotone 101, which was the first device approved by the FDA. All subsequent CES devices have been cleared for marketing by FDA based on the concept of claiming equivalency to the Neurotone 101. The status of cranial electrical stimulation devices and FDA regulation remains a matter of some controversy
Member of
Cataloging source
NLM
http://library.link/vocab/creatorName
Shekelle, Paul G
Funding information
Prepared for: Department of Veterans Affairs, Veterans Health Administration, Quality Enhancement Research Initiative, Health Services Research & Development Service, Washington, DC 20420. Prepared by: Evidence-based Synthesis Program (ESP), West Los Angeles VA Medical Center, Los Angeles, CA, Paul G. Shekelle, MD, PhD, Director
Government publication
federal national government publication
Illustrations
illustrations
Index
no index present
Literary form
non fiction
Nature of contents
  • dictionaries
  • surveys of literature
NLM call number
WB 495
http://library.link/vocab/relatedWorkOrContributorName
  • Cook, Ian Ainsworth
  • West Los Angeles VA Medical Center
  • United States
Series statement
Evidence-based synthesis program
http://library.link/vocab/subjectName
  • Electric Stimulation Therapy
  • Pain Management
  • Depressive Disorder
  • Anxiety Disorders
  • Stress Disorders, Post-Traumatic
  • Sleep Initiation and Maintenance Disorders
Label
The effectiveness and risks of cranial electrical stimulation for the treatment of pain, depression, anxiety, PTSD, and insomnia : a systematic review, principal investigator, Paul Shekelle, Ian Cook; research associates, Isomi M Miake-Lye, Selene Mak, Marika Suttorp Booth, Roberta Shanman, Jessica M Beroes
Instantiates
Publication
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Control code
1046096316
Dimensions
unknown
Extent
1 online resource (1 PDF file (50 pages))
Form of item
online
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations.
Specific material designation
remote
System control number
(OCoLC)1046096316
Label
The effectiveness and risks of cranial electrical stimulation for the treatment of pain, depression, anxiety, PTSD, and insomnia : a systematic review, principal investigator, Paul Shekelle, Ian Cook; research associates, Isomi M Miake-Lye, Selene Mak, Marika Suttorp Booth, Roberta Shanman, Jessica M Beroes
Publication
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Control code
1046096316
Dimensions
unknown
Extent
1 online resource (1 PDF file (50 pages))
Form of item
online
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations.
Specific material designation
remote
System control number
(OCoLC)1046096316

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