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Clinical Trial Summary

A randomized double-blind controlled two centers study. The primary objective of this study will be to show a superiority of hypnosis over relaxation on pain intensity in patients with neuropathic pain.


Clinical Trial Description

The secondary objectives of this study are: - to show a superiority of hypnosis and relaxation over control group on neuropathic pain. - to show a lasting effect of treatment on neuropathic pain one week after the end of treatment. - to evaluate the clinical predictors of response to hypnosis (nature of neuropathic symptoms, severity of anxiety and depressive symptoms, pain catastrophizing, coping strategies, emotional regulation, response to the first session, positive or negative emotional reaction at the end of hypnosis sessions). - to evaluate the effect of hypnosis at long-term (1, 3 and 6 months after the end of treatment). - to evaluate the effect of hypnosis on emotional processes. - to compare hypnosis to relaxation on short-term effects on pain, - to evaluate the quality of life and the impact of pain on daily life: sleep, mood, anxiety symptoms, analgesics consumption , neuropathic symptoms, affective component of pain and pain catastrophizing. 35 patients will be enrolled in each arm, to obtain 105 in total (3 arms). Total duration for each patient: 8 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02256371
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date June 22, 2021

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