Mohamed Sakel, Christine A Ozolins, Karen Saunders, Riya Biswas
{"title":"基于家庭的脑电图神经反馈治疗慢性神经性疼痛的初步研究。","authors":"Mohamed Sakel, Christine A Ozolins, Karen Saunders, Riya Biswas","doi":"10.3389/fpain.2025.1479914","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This study assessed the effect of an 8-week home-based neurofeedback intervention in chronic neuropathic pain patients.</p><p><strong>Subjects/patients: </strong>A cohort of eleven individuals with chronic neuropathic pain receiving treatment within the NHS framework.</p><p><strong>Methods: </strong>Participants were trained to operate a home-based neurofeedback system. Each received a portable Axon system for one week of electroencephalogram (EEG) baselines, followed by an 8-week neurofeedback intervention, and subsequent 12 weeks of follow-up EEG baselines. Primary outcome measures included changes in the Brief Pain Inventory and Visual Analogue Pain Scale at post-intervention, and follow-ups compared with the baseline. Secondary outcomes included changes in depression, anxiety, stress, pain catastrophizing, central sensitization, sleep quality, and quality of life. EEG activities were monitored throughout the trial.</p><p><strong>Results: </strong>Significant improvements were noted in pain scores, with all participants experiencing overall pain reduction. Clinically significant pain improvement (≥30%) was reported by 5 participants (56%). Mood scores showed a significant decrease in depression (<i>p</i> < 0.05), and pain catastrophizing (<i>p</i> < 0.05) scores improved significantly at post-intervention, with continued improvement at the first-month follow-up.</p><p><strong>Conclusion: </strong>The findings indicate that an 8-week home-based neurofeedback intervention improved pain and psychological well-being in this sample of chronic neuropathic pain patients. A randomized controlled trial is required to replicate these results in a larger cohort. <b>Clinical Trial Registration:</b> https://clinicaltrials.gov/study/NCT05464199, identifier: (NCT05464199).</p>","PeriodicalId":73097,"journal":{"name":"Frontiers in pain research (Lausanne, Switzerland)","volume":"6 ","pages":"1479914"},"PeriodicalIF":2.5000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11933074/pdf/","citationCount":"0","resultStr":"{\"title\":\"A home-based EEG neurofeedback treatment for chronic neuropathic pain-a pilot study.\",\"authors\":\"Mohamed Sakel, Christine A Ozolins, Karen Saunders, Riya Biswas\",\"doi\":\"10.3389/fpain.2025.1479914\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>This study assessed the effect of an 8-week home-based neurofeedback intervention in chronic neuropathic pain patients.</p><p><strong>Subjects/patients: </strong>A cohort of eleven individuals with chronic neuropathic pain receiving treatment within the NHS framework.</p><p><strong>Methods: </strong>Participants were trained to operate a home-based neurofeedback system. Each received a portable Axon system for one week of electroencephalogram (EEG) baselines, followed by an 8-week neurofeedback intervention, and subsequent 12 weeks of follow-up EEG baselines. Primary outcome measures included changes in the Brief Pain Inventory and Visual Analogue Pain Scale at post-intervention, and follow-ups compared with the baseline. Secondary outcomes included changes in depression, anxiety, stress, pain catastrophizing, central sensitization, sleep quality, and quality of life. EEG activities were monitored throughout the trial.</p><p><strong>Results: </strong>Significant improvements were noted in pain scores, with all participants experiencing overall pain reduction. Clinically significant pain improvement (≥30%) was reported by 5 participants (56%). Mood scores showed a significant decrease in depression (<i>p</i> < 0.05), and pain catastrophizing (<i>p</i> < 0.05) scores improved significantly at post-intervention, with continued improvement at the first-month follow-up.</p><p><strong>Conclusion: </strong>The findings indicate that an 8-week home-based neurofeedback intervention improved pain and psychological well-being in this sample of chronic neuropathic pain patients. A randomized controlled trial is required to replicate these results in a larger cohort. <b>Clinical Trial Registration:</b> https://clinicaltrials.gov/study/NCT05464199, identifier: (NCT05464199).</p>\",\"PeriodicalId\":73097,\"journal\":{\"name\":\"Frontiers in pain research (Lausanne, Switzerland)\",\"volume\":\"6 \",\"pages\":\"1479914\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-03-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11933074/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in pain research (Lausanne, Switzerland)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/fpain.2025.1479914\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in pain research (Lausanne, Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fpain.2025.1479914","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
A home-based EEG neurofeedback treatment for chronic neuropathic pain-a pilot study.
Objective: This study assessed the effect of an 8-week home-based neurofeedback intervention in chronic neuropathic pain patients.
Subjects/patients: A cohort of eleven individuals with chronic neuropathic pain receiving treatment within the NHS framework.
Methods: Participants were trained to operate a home-based neurofeedback system. Each received a portable Axon system for one week of electroencephalogram (EEG) baselines, followed by an 8-week neurofeedback intervention, and subsequent 12 weeks of follow-up EEG baselines. Primary outcome measures included changes in the Brief Pain Inventory and Visual Analogue Pain Scale at post-intervention, and follow-ups compared with the baseline. Secondary outcomes included changes in depression, anxiety, stress, pain catastrophizing, central sensitization, sleep quality, and quality of life. EEG activities were monitored throughout the trial.
Results: Significant improvements were noted in pain scores, with all participants experiencing overall pain reduction. Clinically significant pain improvement (≥30%) was reported by 5 participants (56%). Mood scores showed a significant decrease in depression (p < 0.05), and pain catastrophizing (p < 0.05) scores improved significantly at post-intervention, with continued improvement at the first-month follow-up.
Conclusion: The findings indicate that an 8-week home-based neurofeedback intervention improved pain and psychological well-being in this sample of chronic neuropathic pain patients. A randomized controlled trial is required to replicate these results in a larger cohort. Clinical Trial Registration: https://clinicaltrials.gov/study/NCT05464199, identifier: (NCT05464199).