A brief cognitive-behavioural intervention for pain reduces secondary hyperalgesia

A brief cognitive behavioural intervention reduces pain unpleasantness and secondary hyperalgesia elicited by repeated nociceptive thermal stimuli. Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. Th...

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Published inPain (Amsterdam) Vol. 155; no. 8; pp. 1446 - 1452
Main Authors Salomons, Tim V., Moayedi, Massieh, Erpelding, Nathalie, Davis, Karen D.
Format Journal Article
LanguageEnglish
Published Philadelphia, PA Elsevier B.V 01.08.2014
International Association for the Study of Pain
Elsevier
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Abstract A brief cognitive behavioural intervention reduces pain unpleasantness and secondary hyperalgesia elicited by repeated nociceptive thermal stimuli. Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. The ability to reverse this sensitization in a top-down manner would be of tremendous clinical benefit, but the degree that this can be accomplished volitionally remains unknown. Here we investigated whether a brief (∼5min) cognitive-behavioural intervention could modify pain perception and reduce central sensitization (as reflected by secondary hyperalgesia). In each of 8 sessions, 2 groups of healthy human subjects received a series of painful thermal stimuli that resulted in secondary hyperalgesia. One group (regulate) was given brief pain-focused cognitive training at each session, while the other group (control) received a non-pain-focused intervention. The intervention selectively reduced pain unpleasantness but not pain intensity in the regulate group. Furthermore, secondary hyperalgesia was significantly reduced in the regulate group compared with the control group. Reduction in secondary hyperalgesia was associated with reduced pain catastrophizing, suggesting that changes in central sensitization are related to changes in pain-related cognitions. Thus, we demonstrate that central sensitization can be modified volitionally by altering pain-related thoughts.
AbstractList Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. The ability to reverse this sensitization in a top-down manner would be of tremendous clinical benefit, but the degree that this can be accomplished volitionally remains unknown. Here we investigated whether a brief (~5 min) cognitive-behavioural intervention could modify pain perception and reduce central sensitization (as reflected by secondary hyperalgesia). In each of 8 sessions, 2 groups of healthy human subjects received a series of painful thermal stimuli that resulted in secondary hyperalgesia. One group (regulate) was given brief pain-focused cognitive training at each session, while the other group (control) received a non-pain-focused intervention. The intervention selectively reduced pain unpleasantness but not pain intensity in the regulate group. Furthermore, secondary hyperalgesia was significantly reduced in the regulate group compared with the control group. Reduction in secondary hyperalgesia was associated with reduced pain catastrophizing, suggesting that changes in central sensitization are related to changes in pain-related cognitions. Thus, we demonstrate that central sensitization can be modified volitionally by altering pain-related thoughts.Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. The ability to reverse this sensitization in a top-down manner would be of tremendous clinical benefit, but the degree that this can be accomplished volitionally remains unknown. Here we investigated whether a brief (~5 min) cognitive-behavioural intervention could modify pain perception and reduce central sensitization (as reflected by secondary hyperalgesia). In each of 8 sessions, 2 groups of healthy human subjects received a series of painful thermal stimuli that resulted in secondary hyperalgesia. One group (regulate) was given brief pain-focused cognitive training at each session, while the other group (control) received a non-pain-focused intervention. The intervention selectively reduced pain unpleasantness but not pain intensity in the regulate group. Furthermore, secondary hyperalgesia was significantly reduced in the regulate group compared with the control group. Reduction in secondary hyperalgesia was associated with reduced pain catastrophizing, suggesting that changes in central sensitization are related to changes in pain-related cognitions. Thus, we demonstrate that central sensitization can be modified volitionally by altering pain-related thoughts.
A brief cognitive behavioural intervention reduces pain unpleasantness and secondary hyperalgesia elicited by repeated nociceptive thermal stimuli. Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. The ability to reverse this sensitization in a top-down manner would be of tremendous clinical benefit, but the degree that this can be accomplished volitionally remains unknown. Here we investigated whether a brief (∼5min) cognitive-behavioural intervention could modify pain perception and reduce central sensitization (as reflected by secondary hyperalgesia). In each of 8 sessions, 2 groups of healthy human subjects received a series of painful thermal stimuli that resulted in secondary hyperalgesia. One group (regulate) was given brief pain-focused cognitive training at each session, while the other group (control) received a non-pain-focused intervention. The intervention selectively reduced pain unpleasantness but not pain intensity in the regulate group. Furthermore, secondary hyperalgesia was significantly reduced in the regulate group compared with the control group. Reduction in secondary hyperalgesia was associated with reduced pain catastrophizing, suggesting that changes in central sensitization are related to changes in pain-related cognitions. Thus, we demonstrate that central sensitization can be modified volitionally by altering pain-related thoughts.
Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. The ability to reverse this sensitization in a top-down manner would be of tremendous clinical benefit, but the degree that this can be accomplished volitionally remains unknown. Here we investigated whether a brief (~5 min) cognitive-behavioural intervention could modify pain perception and reduce central sensitization (as reflected by secondary hyperalgesia). In each of 8 sessions, 2 groups of healthy human subjects received a series of painful thermal stimuli that resulted in secondary hyperalgesia. One group (regulate) was given brief pain-focused cognitive training at each session, while the other group (control) received a non-pain-focused intervention. The intervention selectively reduced pain unpleasantness but not pain intensity in the regulate group. Furthermore, secondary hyperalgesia was significantly reduced in the regulate group compared with the control group. Reduction in secondary hyperalgesia was associated with reduced pain catastrophizing, suggesting that changes in central sensitization are related to changes in pain-related cognitions. Thus, we demonstrate that central sensitization can be modified volitionally by altering pain-related thoughts.
Author Salomons, Tim V.
Moayedi, Massieh
Erpelding, Nathalie
Davis, Karen D.
AuthorAffiliation Division of Brain, Imaging and Behaviour—Systems Neuroscience, Toronto Western Research Institute, Toronto, Ontario, Canada Department of Psychiatry, University Health Network, Canada School of Psychology and Clinical Language Sciences, University of Reading, Reading, UK Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK Department of Surgery, University of Toronto, Toronto, Ontario, Canada
AuthorAffiliation_xml – name: Division of Brain, Imaging and Behaviour—Systems Neuroscience, Toronto Western Research Institute, Toronto, Ontario, Canada Department of Psychiatry, University Health Network, Canada School of Psychology and Clinical Language Sciences, University of Reading, Reading, UK Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK Department of Surgery, University of Toronto, Toronto, Ontario, Canada
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Issue 8
Keywords Allodynia
Secondary hyperalgesia
CBT
Catastrophizing
Unpleasantness
Nervous system diseases
Cognitive therapy
Treatment
Pain
Pleasure unpleasure
Behavior therapy
Hyperalgesia
Language English
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Snippet A brief cognitive behavioural intervention reduces pain unpleasantness and secondary hyperalgesia elicited by repeated nociceptive thermal stimuli. Repeated...
Repeated exposure to pain can result in sensitization of the central nervous system, enhancing subsequent pain and potentially leading to chronicity. The...
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Enrichment Source
Publisher
StartPage 1446
SubjectTerms Adult
Allodynia
Behavior therapy. Cognitive therapy
Biological and medical sciences
Catastrophizing
CBT
Cognitive Behavioral Therapy - methods
Female
Hot Temperature
Humans
Hyperalgesia - psychology
Hyperalgesia - therapy
Male
Medical sciences
Nervous system (semeiology, syndromes)
Nervous system as a whole
Neurology
Pain - psychology
Pain Management - methods
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychotherapy, Brief - methods
Secondary hyperalgesia
Treatment Outcome
Treatments
Unpleasantness
Young Adult
Title A brief cognitive-behavioural intervention for pain reduces secondary hyperalgesia
URI https://dx.doi.org/10.1016/j.pain.2014.02.012
https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00006396-201408000-00008
https://www.ncbi.nlm.nih.gov/pubmed/24569149
https://www.proquest.com/docview/1547520051
https://www.proquest.com/docview/1677319287
Volume 155
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