Charlotte C M van Laake-Geelen, Rob J E M Smeets, Marielle E J B Goossens, Jeanine A Verbunt
{"title":"对糖尿病疼痛性神经病患者进行体内暴露的有效性:关于对身体活动和生活质量影响的试点研究。","authors":"Charlotte C M van Laake-Geelen, Rob J E M Smeets, Marielle E J B Goossens, Jeanine A Verbunt","doi":"10.2340/20030711-1000046","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the effects of personalized exposure <i>in vivo</i> on level of physical activity and quality of life in patients with painful diabetic neuropathy.</p><p><strong>Design: </strong>Randomized, single-case, ABC design.</p><p><strong>Subjects: </strong>Twelve patients with painful diabetic neuropathy, age > 18 years, diabetes mellitus type II, Clinical Neurological Examination score > 5, Diabetic Neuropathy Symptom Score ≥ 1 and Douleur Neuropathique 4 Questions score ≥ 3.</p><p><strong>Methods: </strong>The treatment consists of an Intensive screening, followed by an 8-week exposure <i>in vivo</i> intervention specifically adapted to the needs/risks of patients with painful diabetic neuropathy, and 6-months follow-up. Outcome measures included daily and non-daily measures of physical activity, quality of life, metabolic parameters, disability, depression, general and painful diabetic neuropathy-related anxiety, pain intensity and pain catastrophizing.</p><p><strong>Results: </strong>Due to high drop-out rates (<i>n</i> = 6 during screening, <i>n</i> = 2 during treatment, <i>n</i> = 1 after treatment), only 3 participants completed the study. Slight, but non-significant, changes in physical activity and disability were observed. In quality of life, no changes were observed.</p><p><strong>Conclusion: </strong>Analysis of the reasons for the high drop-out rate indicate that exposure <i>in vivo</i> may have added value in patients with painful diabetic neuropathy only for those patients: (<i>i</i>) whose daily life functioning is impaired mainly by the painful diabetic neuropathy; (<i>ii</i>) in whom painful diabetic neuropathy-related fears are exaggerated and irrational; (<i>iii</i>) in whom specific activities evoke the painful diabetic neuropathy-related fears; (<i>iv</i>) whose spouse and healthcare providers are involved in the treatment; and (<i>v</i>) who are willing to change their daily behaviour. Further research is needed into this subject.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000046"},"PeriodicalIF":0.0000,"publicationDate":"2021-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c2/81/JRMCC-4-1000046.PMC8054751.pdf","citationCount":"0","resultStr":"{\"title\":\"Effectiveness of Exposure in Vivo for Patients with Painful Diabetic Neuropathy: a Pilot Study of Effects on Physical Activity and Quality of Life.\",\"authors\":\"Charlotte C M van Laake-Geelen, Rob J E M Smeets, Marielle E J B Goossens, Jeanine A Verbunt\",\"doi\":\"10.2340/20030711-1000046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To evaluate the effects of personalized exposure <i>in vivo</i> on level of physical activity and quality of life in patients with painful diabetic neuropathy.</p><p><strong>Design: </strong>Randomized, single-case, ABC design.</p><p><strong>Subjects: </strong>Twelve patients with painful diabetic neuropathy, age > 18 years, diabetes mellitus type II, Clinical Neurological Examination score > 5, Diabetic Neuropathy Symptom Score ≥ 1 and Douleur Neuropathique 4 Questions score ≥ 3.</p><p><strong>Methods: </strong>The treatment consists of an Intensive screening, followed by an 8-week exposure <i>in vivo</i> intervention specifically adapted to the needs/risks of patients with painful diabetic neuropathy, and 6-months follow-up. Outcome measures included daily and non-daily measures of physical activity, quality of life, metabolic parameters, disability, depression, general and painful diabetic neuropathy-related anxiety, pain intensity and pain catastrophizing.</p><p><strong>Results: </strong>Due to high drop-out rates (<i>n</i> = 6 during screening, <i>n</i> = 2 during treatment, <i>n</i> = 1 after treatment), only 3 participants completed the study. Slight, but non-significant, changes in physical activity and disability were observed. In quality of life, no changes were observed.</p><p><strong>Conclusion: </strong>Analysis of the reasons for the high drop-out rate indicate that exposure <i>in vivo</i> may have added value in patients with painful diabetic neuropathy only for those patients: (<i>i</i>) whose daily life functioning is impaired mainly by the painful diabetic neuropathy; (<i>ii</i>) in whom painful diabetic neuropathy-related fears are exaggerated and irrational; (<i>iii</i>) in whom specific activities evoke the painful diabetic neuropathy-related fears; (<i>iv</i>) whose spouse and healthcare providers are involved in the treatment; and (<i>v</i>) who are willing to change their daily behaviour. Further research is needed into this subject.</p>\",\"PeriodicalId\":73929,\"journal\":{\"name\":\"Journal of rehabilitation medicine. 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Effectiveness of Exposure in Vivo for Patients with Painful Diabetic Neuropathy: a Pilot Study of Effects on Physical Activity and Quality of Life.
Objective: To evaluate the effects of personalized exposure in vivo on level of physical activity and quality of life in patients with painful diabetic neuropathy.
Design: Randomized, single-case, ABC design.
Subjects: Twelve patients with painful diabetic neuropathy, age > 18 years, diabetes mellitus type II, Clinical Neurological Examination score > 5, Diabetic Neuropathy Symptom Score ≥ 1 and Douleur Neuropathique 4 Questions score ≥ 3.
Methods: The treatment consists of an Intensive screening, followed by an 8-week exposure in vivo intervention specifically adapted to the needs/risks of patients with painful diabetic neuropathy, and 6-months follow-up. Outcome measures included daily and non-daily measures of physical activity, quality of life, metabolic parameters, disability, depression, general and painful diabetic neuropathy-related anxiety, pain intensity and pain catastrophizing.
Results: Due to high drop-out rates (n = 6 during screening, n = 2 during treatment, n = 1 after treatment), only 3 participants completed the study. Slight, but non-significant, changes in physical activity and disability were observed. In quality of life, no changes were observed.
Conclusion: Analysis of the reasons for the high drop-out rate indicate that exposure in vivo may have added value in patients with painful diabetic neuropathy only for those patients: (i) whose daily life functioning is impaired mainly by the painful diabetic neuropathy; (ii) in whom painful diabetic neuropathy-related fears are exaggerated and irrational; (iii) in whom specific activities evoke the painful diabetic neuropathy-related fears; (iv) whose spouse and healthcare providers are involved in the treatment; and (v) who are willing to change their daily behaviour. Further research is needed into this subject.