Pub Date : 2014-01-01Epub Date: 2014-06-16DOI: 10.1159/000357464
Marta Stelmach-Mardas, Jarosław Walkowiak, Paweł Zagrodzki, Bogna Grygiel-Górniak, Juliusz Przysławski
Background: The aim of this study was to assess the influence of increased plant stanol ester intake on lipid profile and serum ratio of non-cholesterol sterols to cholesterol in obese women (50 years of age) with dyslipidemia.
Methods: 90 females were assigned into 2 treatment groups: For a period of 4 weeks, group 1 was receiving a yoghurt, enriched with 2 g of plant stanol ester (PS group), and group 2 was receiving a yoghurt drink without extra stanols. Anthropometric measurements included body height and weight. Lipid profile was determined by commercially available enzymatic methods. Serum non-cholesterol sterols and stanols concentrations were quantitated by gas chromatography. The study was single-blind and placebo-controlled.
Results: The yoghurt drink enriched with plant stanol ester significantly reduced serum total cholesterol, LDL cholesterol, and non-HDL cholesterol levels (p < 0.05). No changes were observed in HDL cholesterol and triacylglycerol levels. The highest drop of LDL cholesterol was noted in the upper quartile of total cholesterol concentrations. In the PS group the statistically significant (p < 0.0001) changes were also observed in serum ratios of non-cholesterol sterols to cholesterol: campesterol, sitosterol, sitostanol, and avenasterol.
Conclusion: Plant stanol esters influence the concentration of total cholesterol, particularly LDL cholesterol. This effect seems to be related to the reduced dietary cholesterol absorption.
{"title":"Lipid profile and non-cholesterol sterols in obese women's serum after supplementing with plant stanol ester.","authors":"Marta Stelmach-Mardas, Jarosław Walkowiak, Paweł Zagrodzki, Bogna Grygiel-Górniak, Juliusz Przysławski","doi":"10.1159/000357464","DOIUrl":"10.1159/000357464","url":null,"abstract":"<p><strong>Background: </strong>The aim of this study was to assess the influence of increased plant stanol ester intake on lipid profile and serum ratio of non-cholesterol sterols to cholesterol in obese women (50 years of age) with dyslipidemia.</p><p><strong>Methods: </strong>90 females were assigned into 2 treatment groups: For a period of 4 weeks, group 1 was receiving a yoghurt, enriched with 2 g of plant stanol ester (PS group), and group 2 was receiving a yoghurt drink without extra stanols. Anthropometric measurements included body height and weight. Lipid profile was determined by commercially available enzymatic methods. Serum non-cholesterol sterols and stanols concentrations were quantitated by gas chromatography. The study was single-blind and placebo-controlled.</p><p><strong>Results: </strong>The yoghurt drink enriched with plant stanol ester significantly reduced serum total cholesterol, LDL cholesterol, and non-HDL cholesterol levels (p < 0.05). No changes were observed in HDL cholesterol and triacylglycerol levels. The highest drop of LDL cholesterol was noted in the upper quartile of total cholesterol concentrations. In the PS group the statistically significant (p < 0.0001) changes were also observed in serum ratios of non-cholesterol sterols to cholesterol: campesterol, sitosterol, sitostanol, and avenasterol.</p><p><strong>Conclusion: </strong>Plant stanol esters influence the concentration of total cholesterol, particularly LDL cholesterol. This effect seems to be related to the reduced dietary cholesterol absorption.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 3","pages":"178-83"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32531884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-01-01Epub Date: 2014-03-17DOI: 10.1159/000360966
Franziska Matzer, Eva Nagele, Babak Bahadori, Karl Dam, Christian Fazekas
Background: Stress-relieving effects of balneotherapy compared to progressive muscle relaxation (PMR) and to resting were investigated by measuring subjective relaxation and salivary cortisol. It was also examined whether participants with a high versus low stress level would have a different relaxation response.
Methods: A sample of healthy volunteers was randomized to balneotherapy, PMR, or a resting control group, each intervention lasting for 25 min. Pre- and post-intervention salivary cortisol samples were collected, and participants rated their status of relaxation on a quantitative scale. In addition, 3 questionnaires were applied to detect participants' stress level and bodily complaints.
Results: 49 healthy participants were recruited (65.3% female). In a pre-post comparison, salivary cortisol decreased (F = 23.53, p < 0.001) and subjective relaxation ratings increased (F = 132.18, p < 0.001) in all 3 groups. Study participants in the balneotherapy group rated themselves as more relaxed after the intervention as compared to the other groups (F = 5.22, p < 0.009). Participants with a high versus low stress level differed in somatic symptoms and in morning cortisol levels, but showed a similar relaxation response.
Conclusion: Findings suggest that compared to PMR and resting, balneotherapy seems to be more beneficial with regard to subjective relaxation effects and similarly beneficial with regard to a decrease in salivary cortisol.
背景:通过测量主观放松和唾液皮质醇,研究了按摩疗法与渐进式肌肉放松(PMR)和休息相比较的压力缓解效果。研究人员还检查了高压力水平和低压力水平的参与者是否会有不同的放松反应。方法:将健康志愿者随机分为沐浴疗法组、PMR组和静息对照组,每次干预持续25分钟。收集干预前和干预后唾液皮质醇样本,参与者以定量量表评估他们的放松状态。此外,还使用3份问卷来检测参与者的压力水平和身体抱怨。结果:49名健康受试者被招募,其中65.3%为女性。在前后比较中,三组唾液皮质醇降低(F = 23.53, p < 0.001),主观放松评分升高(F = 132.18, p < 0.001)。与其他组相比,沐浴疗法组的研究参与者在干预后认为自己更放松(F = 5.22, p < 0.009)。高压力水平和低压力水平的参与者在躯体症状和早晨皮质醇水平上有所不同,但表现出相似的放松反应。结论:研究结果表明,与PMR和休息相比,浴疗似乎在主观放松效果方面更有益,在降低唾液皮质醇方面也同样有益。
{"title":"Stress-relieving effects of short-term balneotherapy - a randomized controlled pilot study in healthy adults.","authors":"Franziska Matzer, Eva Nagele, Babak Bahadori, Karl Dam, Christian Fazekas","doi":"10.1159/000360966","DOIUrl":"https://doi.org/10.1159/000360966","url":null,"abstract":"<p><strong>Background: </strong>Stress-relieving effects of balneotherapy compared to progressive muscle relaxation (PMR) and to resting were investigated by measuring subjective relaxation and salivary cortisol. It was also examined whether participants with a high versus low stress level would have a different relaxation response.</p><p><strong>Methods: </strong>A sample of healthy volunteers was randomized to balneotherapy, PMR, or a resting control group, each intervention lasting for 25 min. Pre- and post-intervention salivary cortisol samples were collected, and participants rated their status of relaxation on a quantitative scale. In addition, 3 questionnaires were applied to detect participants' stress level and bodily complaints.</p><p><strong>Results: </strong>49 healthy participants were recruited (65.3% female). In a pre-post comparison, salivary cortisol decreased (F = 23.53, p < 0.001) and subjective relaxation ratings increased (F = 132.18, p < 0.001) in all 3 groups. Study participants in the balneotherapy group rated themselves as more relaxed after the intervention as compared to the other groups (F = 5.22, p < 0.009). Participants with a high versus low stress level differed in somatic symptoms and in morning cortisol levels, but showed a similar relaxation response.</p><p><strong>Conclusion: </strong>Findings suggest that compared to PMR and resting, balneotherapy seems to be more beneficial with regard to subjective relaxation effects and similarly beneficial with regard to a decrease in salivary cortisol.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 2","pages":"105-10"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000360966","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32359309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-01-01Epub Date: 2014-07-04DOI: 10.1159/000362394
Reinhard Saller, Jörg Melzer, Günter Meng, Ursula von Mandach, Karin Fürer, Herbert Schwabl, Cecile Vennos
ePerinatale Pharmakologie, UniversitatsSpital Zurich, f Padma AG, Hinwil, Schweiz Die moderne Phytotherapie ist im Rahmen ihrer materiellen Moglichkeiten ein durchaus forschungsaffiner Therapiebereich. Neben einem mehrdimensionalen Ansatz, anhand einer Heilpflanze beispielhaft ein potentiel les phytotherapeutisches Therapiespektrum auszuloten geht es vor allem um eine reflektierte wissenschaftliche Auseinandersetzung mit Methodologie, Aussagekraft und notwendigen Modifizierungen von Metaanalysen sowie mit Ansatzen aus der Versorgungsforschung. Beide Vorgehensweisen bilden derzeit auch in der Phytotherapie einen viel beachteten Fokus der klinischen und klinisch-epidemiologischen Forschung. Die Metaanalysen beschaftigen sich naturgemas mit bereits vorhandenen Studiendaten und treffen dabei jeweils eine begrundete wenngleich selektive und forscherbezogen durchaus subjektive Auswahl. Spezifische phytothera peutische Gesichtspunkte wie z.B. Besonderheiten von Extrakten oder Vergleichbarkeit von Phytotherapeutika werden bislang kaum wissenschaftlich angemessen berucksichtigt. In der Versorgungsforschung, die nicht durch fixe Studienvorgaben eingeschrankt ist, stehen Daten aus der flexiblen und variablen Praxis im Vorder grund. Dieser Ansatz kann es, bei allen Einschrankungen, ermoglichen, neue und therapierelevante Gesichtspunkte zu entdecken, z.B. im Hinblick auf Dosierungen. Der authentische Charakter von Phytotherapeutika als Vielstoffgemische in stofflicher und funktioneller Hin sicht mit genuinen pleiotropen Eigenschaften wird bislang in der Forschung, vor allem der pharmakologischen Forschung, nur selten adaquat aufgegriffen. Vergleichbar werden pflanzliche Arzneimittel noch im mer praferentiell unter dem eher realitatsfernen Grundsatz gesehen: «one drug, one indication». Die Betrachtung und Beforschung von Phytotherapeutika als Netzwerkarzneimittel mit pleiotropen Signaturen weist auf zukunfstrachtige Vorgehensweisen hin.
{"title":"[Efficacy in phytotherapy].","authors":"Reinhard Saller, Jörg Melzer, Günter Meng, Ursula von Mandach, Karin Fürer, Herbert Schwabl, Cecile Vennos","doi":"10.1159/000362394","DOIUrl":"https://doi.org/10.1159/000362394","url":null,"abstract":"ePerinatale Pharmakologie, UniversitatsSpital Zurich, f Padma AG, Hinwil, Schweiz Die moderne Phytotherapie ist im Rahmen ihrer materiellen Moglichkeiten ein durchaus forschungsaffiner Therapiebereich. Neben einem mehrdimensionalen Ansatz, anhand einer Heilpflanze beispielhaft ein potentiel les phytotherapeutisches Therapiespektrum auszuloten geht es vor allem um eine reflektierte wissenschaftliche Auseinandersetzung mit Methodologie, Aussagekraft und notwendigen Modifizierungen von Metaanalysen sowie mit Ansatzen aus der Versorgungsforschung. Beide Vorgehensweisen bilden derzeit auch in der Phytotherapie einen viel beachteten Fokus der klinischen und klinisch-epidemiologischen Forschung. Die Metaanalysen beschaftigen sich naturgemas mit bereits vorhandenen Studiendaten und treffen dabei jeweils eine begrundete wenngleich selektive und forscherbezogen durchaus subjektive Auswahl. Spezifische phytothera peutische Gesichtspunkte wie z.B. Besonderheiten von Extrakten oder Vergleichbarkeit von Phytotherapeutika werden bislang kaum wissenschaftlich angemessen berucksichtigt. In der Versorgungsforschung, die nicht durch fixe Studienvorgaben eingeschrankt ist, stehen Daten aus der flexiblen und variablen Praxis im Vorder grund. Dieser Ansatz kann es, bei allen Einschrankungen, ermoglichen, neue und therapierelevante Gesichtspunkte zu entdecken, z.B. im Hinblick auf Dosierungen. Der authentische Charakter von Phytotherapeutika als Vielstoffgemische in stofflicher und funktioneller Hin sicht mit genuinen pleiotropen Eigenschaften wird bislang in der Forschung, vor allem der pharmakologischen Forschung, nur selten adaquat aufgegriffen. Vergleichbar werden pflanzliche Arzneimittel noch im mer praferentiell unter dem eher realitatsfernen Grundsatz gesehen: «one drug, one indication». Die Betrachtung und Beforschung von Phytotherapeutika als Netzwerkarzneimittel mit pleiotropen Signaturen weist auf zukunfstrachtige Vorgehensweisen hin.","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 Suppl 1 ","pages":"19-28"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000362394","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32494545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-01-01Epub Date: 2014-02-17DOI: 10.1159/000358742
You-Jung Kwon, Seunghoon Lee, Sangmin Park, Ungin Lee, Sung-Keun Lim, Dongwoo Nam, Sanghoon Lee
Background: The aim of this study was to investigate the effects of needle-pricking therapy on peripheral facial paralysis.
Methods: This study included 162 patients with peripheral facial paralysis, 107 of whom were treated with usual care (conventional and alternative treatments) and 55 of whom were additionally treated with needle-pricking therapy on 3 specific extra-meridian acupuncture points known as 'Samjoong' (Sānchóng in Chinese). We evaluated changes in facial motor functions and sequelae using the Yanagihara and gross House-Brackmann grading systems before and after treatments.
Results: Yanagihara score and House-Brackmann grade significantly improved after treatments in both groups. However, the needle-pricking therapy group showed greater improvements in Yanagihara score and House-Brackmann grade than the usual care group.
Conclusion: Our results suggest that Samjoong needle-pricking therapy could be applied as an adjunct therapy to usual care for patients with peripheral facial paralysis.
{"title":"Clinical effects of needle-pricking therapy on peripheral facial paralysis.","authors":"You-Jung Kwon, Seunghoon Lee, Sangmin Park, Ungin Lee, Sung-Keun Lim, Dongwoo Nam, Sanghoon Lee","doi":"10.1159/000358742","DOIUrl":"https://doi.org/10.1159/000358742","url":null,"abstract":"<p><strong>Background: </strong>The aim of this study was to investigate the effects of needle-pricking therapy on peripheral facial paralysis.</p><p><strong>Methods: </strong>This study included 162 patients with peripheral facial paralysis, 107 of whom were treated with usual care (conventional and alternative treatments) and 55 of whom were additionally treated with needle-pricking therapy on 3 specific extra-meridian acupuncture points known as 'Samjoong' (Sānchóng in Chinese). We evaluated changes in facial motor functions and sequelae using the Yanagihara and gross House-Brackmann grading systems before and after treatments.</p><p><strong>Results: </strong>Yanagihara score and House-Brackmann grade significantly improved after treatments in both groups. However, the needle-pricking therapy group showed greater improvements in Yanagihara score and House-Brackmann grade than the usual care group.</p><p><strong>Conclusion: </strong>Our results suggest that Samjoong needle-pricking therapy could be applied as an adjunct therapy to usual care for patients with peripheral facial paralysis.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 1","pages":"14-8"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000358742","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40288676","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-01-01Epub Date: 2014-02-18DOI: 10.1159/000358176
Klaus Blaser, Milena Zlabinger, Thilo Hinterberger
Background: The Interpersonal Attention Management Inventory (IAMI) represents a new instrument to capture self- and external perception skills. The underlying theoretical model assumes 3 mental locations of attention (the intrapersonal space, the extrapersonal space, and the external intrapersonal space) of the other.
Methods: The IAMI was studied regarding its factor structure; it was shortened and statistical values as well as first reference values were calculated based on a larger sample (n = 1089).
Results: By factor analysis, the superordinate scales could be widely validated. The shortened version with 31 items and 3 superordinate scales shows a high reliability of the global value (Cronbach's α = 0.81) and, regarding the convergent validity, a modest correlation (r = 0.41) of the global value and mindfulness, measured with the Freiburg Mindfulness Inventory (FMI).
Conclusions: Further validation studies are invited so that the IAMI can be used as an instrument for (course) diagnosis in the therapy of psychiatric disorders as well as for research in social neuroscience, e.g., in investigations on mindfulness, compassion, empathy, theory of mind, and self-boundaries.
{"title":"[Interpersonal attention management inventory: a new instrument to capture different self- and external perception skills].","authors":"Klaus Blaser, Milena Zlabinger, Thilo Hinterberger","doi":"10.1159/000358176","DOIUrl":"https://doi.org/10.1159/000358176","url":null,"abstract":"<p><strong>Background: </strong>The Interpersonal Attention Management Inventory (IAMI) represents a new instrument to capture self- and external perception skills. The underlying theoretical model assumes 3 mental locations of attention (the intrapersonal space, the extrapersonal space, and the external intrapersonal space) of the other.</p><p><strong>Methods: </strong>The IAMI was studied regarding its factor structure; it was shortened and statistical values as well as first reference values were calculated based on a larger sample (n = 1089).</p><p><strong>Results: </strong>By factor analysis, the superordinate scales could be widely validated. The shortened version with 31 items and 3 superordinate scales shows a high reliability of the global value (Cronbach's α = 0.81) and, regarding the convergent validity, a modest correlation (r = 0.41) of the global value and mindfulness, measured with the Freiburg Mindfulness Inventory (FMI).</p><p><strong>Conclusions: </strong>Further validation studies are invited so that the IAMI can be used as an instrument for (course) diagnosis in the therapy of psychiatric disorders as well as for research in social neuroscience, e.g., in investigations on mindfulness, compassion, empathy, theory of mind, and self-boundaries.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 1","pages":"34-41"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000358176","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40288679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: An open-label pilot study of individualized homeopathy for attention deficit hyperactivity disorder (ADHD) was conducted to assess the potential for future studies with a focus on the feasibility of the recruitment plan and outcome measure schedules; identification of any group characteristics of participants who respond significantly to the therapy; and establishing the length of time required for an improvement in ADHD symptoms.
Patients and methods: Participants (aged 6-16) were recruited through community advertisement and outreach. Participants completed 1 screening and 9 individualized homeopathic follow-up consultations. ADHD symptoms were assessed using the Conners 3 - Parent Questionnaire administered at each consultation. The pre- and post-study difference in Conners Global Index - Parent (CGI-P) T-score was evaluated for each participant. Baseline data of those who showed a statistically significant improvement (responders) were compared to those who did not (non-responders).
Results: 35 participants were enrolled over 11 months. 80% completed all 10 consultations in a median of 12.1 months. 63% had a statistically significant improvement in the primary outcome, first occurring after a mean of 4.5 visits. Overall scores for participants completing at least 2 data points decreased from a baseline median of 85.5 to 74.0 (p < 0.001, CI 95%). There were no significant baseline differences between responders and non-responders. No serious adverse events related to the therapy were reported.
Conclusion: The change in the median CGI-P T-score from baseline to the end of this open-label pilot study was statistically significant. The research methods are feasible. Future studies are warranted.
Trial registration: NCT01141634.
背景:进行了一项针对注意缺陷多动障碍(ADHD)的个体化顺势疗法的开放标签试点研究,以评估未来研究的潜力,重点关注招募计划和结果测量时间表的可行性;确定对治疗有显著反应的参与者的任何群体特征;并确定改善ADHD症状所需的时间长度。患者和方法:通过社区广告和外展招募参与者(6-16岁)。参与者完成了1次筛查和9次个体化顺势疗法随访咨询。ADHD症状在每次咨询时使用Conners 3 - Parent Questionnaire进行评估。评估每个参与者的Conners Global Index - Parent (CGI-P) T-score在研究前和研究后的差异。基线数据显示有统计学显著改善的患者(应答者)与无应答者(无应答者)进行比较。结果:35名参与者在11个月的时间里被纳入研究。80%的患者在12.1个月的中位数时间内完成了所有10次咨询。63%的患者在主要结果上有统计学意义上的显著改善,首次出现在平均4.5次就诊后。完成至少2个数据点的参与者的总得分从基线中位数85.5下降到74.0 (p < 0.001, CI 95%)。在应答者和无应答者之间没有显著的基线差异。未见与治疗相关的严重不良事件的报道。结论:从基线到这项开放标签先导研究结束时,中位CGI-P t评分的变化具有统计学意义。研究方法是可行的。未来的研究是有必要的。试验注册:NCT01141634。
{"title":"An open-label pilot study of homeopathic treatment of attention deficit hyperactivity disorder in children and youth.","authors":"David Brulé, Lauren Sule, Beth Landau-Halpern, Violeta Nastase, Umesh Jain, Sunita Vohra, Heather Boon","doi":"10.1159/000368137","DOIUrl":"https://doi.org/10.1159/000368137","url":null,"abstract":"<p><strong>Background: </strong>An open-label pilot study of individualized homeopathy for attention deficit hyperactivity disorder (ADHD) was conducted to assess the potential for future studies with a focus on the feasibility of the recruitment plan and outcome measure schedules; identification of any group characteristics of participants who respond significantly to the therapy; and establishing the length of time required for an improvement in ADHD symptoms.</p><p><strong>Patients and methods: </strong>Participants (aged 6-16) were recruited through community advertisement and outreach. Participants completed 1 screening and 9 individualized homeopathic follow-up consultations. ADHD symptoms were assessed using the Conners 3 - Parent Questionnaire administered at each consultation. The pre- and post-study difference in Conners Global Index - Parent (CGI-P) T-score was evaluated for each participant. Baseline data of those who showed a statistically significant improvement (responders) were compared to those who did not (non-responders).</p><p><strong>Results: </strong>35 participants were enrolled over 11 months. 80% completed all 10 consultations in a median of 12.1 months. 63% had a statistically significant improvement in the primary outcome, first occurring after a mean of 4.5 visits. Overall scores for participants completing at least 2 data points decreased from a baseline median of 85.5 to 74.0 (p < 0.001, CI 95%). There were no significant baseline differences between responders and non-responders. No serious adverse events related to the therapy were reported.</p><p><strong>Conclusion: </strong>The change in the median CGI-P T-score from baseline to the end of this open-label pilot study was statistically significant. The research methods are feasible. Future studies are warranted.</p><p><strong>Trial registration: </strong>NCT01141634.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 5","pages":"302-9"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000368137","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32839413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-01-01Epub Date: 2014-02-17DOI: 10.1159/000358725
Rachel Canaway, Lenore Manderson, Brian Oldenburg
Background: Little is known about why and how people with type 2 diabetes and cardiovascular disease (CVD) use CAM, or of the perceived benefits of CAM use. The CAMELOT study explored care-seeking, self-management, costs, barriers and benefits of CAM use among this population. We report here on CAM used for treatment of diabetes and CVD, and non-clinical outcomes of CAM use.
Methods: Data were collected in 2009-2010 via in-depth interviews (n = 69) and a self-report questionnaire (n = 2,915) among people with diabetes and/or CVD, throughout an Australian state. Analysis included contingency tables, chi-square analysis and thematic coding of interview and long answer survey data.
Results: CAM use was generally part of a multi-component approach to chronic condition management. Choice of CAM practitioners and products varied and included CAM not usually associated with diabetes or CVD treatment, such as massage or manipulative therapies (44%). Most survey respondents perceived that CAM consultations resulted in symptom relief, improved general health and increased knowledge, understanding and confidence in condition management. Few people reported that they experienced any side effects from CAM. Economic barriers were significant in limiting access to CAM.
Conclusion: More research is required to understand how the appropriate use and perceived benefits of CAM can be reinforced by stronger interaction or integration with mainstream health service delivery for chronic condition management and illness prevention.
{"title":"Perceptions of benefit of complementary therapy use among people with diabetes and cardiovascular disease.","authors":"Rachel Canaway, Lenore Manderson, Brian Oldenburg","doi":"10.1159/000358725","DOIUrl":"https://doi.org/10.1159/000358725","url":null,"abstract":"<p><strong>Background: </strong>Little is known about why and how people with type 2 diabetes and cardiovascular disease (CVD) use CAM, or of the perceived benefits of CAM use. The CAMELOT study explored care-seeking, self-management, costs, barriers and benefits of CAM use among this population. We report here on CAM used for treatment of diabetes and CVD, and non-clinical outcomes of CAM use.</p><p><strong>Methods: </strong>Data were collected in 2009-2010 via in-depth interviews (n = 69) and a self-report questionnaire (n = 2,915) among people with diabetes and/or CVD, throughout an Australian state. Analysis included contingency tables, chi-square analysis and thematic coding of interview and long answer survey data.</p><p><strong>Results: </strong>CAM use was generally part of a multi-component approach to chronic condition management. Choice of CAM practitioners and products varied and included CAM not usually associated with diabetes or CVD treatment, such as massage or manipulative therapies (44%). Most survey respondents perceived that CAM consultations resulted in symptom relief, improved general health and increased knowledge, understanding and confidence in condition management. Few people reported that they experienced any side effects from CAM. Economic barriers were significant in limiting access to CAM.</p><p><strong>Conclusion: </strong>More research is required to understand how the appropriate use and perceived benefits of CAM can be reinforced by stronger interaction or integration with mainstream health service delivery for chronic condition management and illness prevention.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 1","pages":"25-33"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000358725","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40288678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-01-01Epub Date: 2014-02-17DOI: 10.1159/000358571
Hossein Bamfarahnak, Amir Azizi, Ali Noorafshan, Abdolali Mohagheghzadeh
Cupping therapy (CT) is one of the oldest medical techniques available, and is still used in several cultures instead of or as an adjunct or complement to 'western academic' medicine. Moreover, CT (wet or dry) is claimed to have therapeutic effects in many types of disorders which do not fully respond to conventional medicine or for which no effective treatment is available. However, no recent reviews of the clinical practice of cupping are available to the best of our knowledge. We describe the applications of CT as used in Traditional Iranian Medicine (TIM). Several databases were searched for relevant literature. In addition, we studied the main traditional treatises on TIM regarding the history and practice of CT. Information about current practices was obtained from a systematic survey among practitioners. Our results suggest that CT is currently prescribed for up to 120 diseases and disorders that are difficult to treat, including cutaneous (21.7%), musculoskeletal (15%), and central nervous system (13.3%) disorders. Moreover, TIM treatises note 25 specific sites on the body surface which correspond to certain diseases, and on which wet-cupping therapy has therapeutic effects. Additional clinical studies of CT may lead to findings on new therapeutic methods and may shed light on mechanisms of disease and illness that are not fully understood in conventional medicine.
{"title":"A tale of Persian cupping therapy: 1001 potential applications and avenues for research.","authors":"Hossein Bamfarahnak, Amir Azizi, Ali Noorafshan, Abdolali Mohagheghzadeh","doi":"10.1159/000358571","DOIUrl":"https://doi.org/10.1159/000358571","url":null,"abstract":"<p><p>Cupping therapy (CT) is one of the oldest medical techniques available, and is still used in several cultures instead of or as an adjunct or complement to 'western academic' medicine. Moreover, CT (wet or dry) is claimed to have therapeutic effects in many types of disorders which do not fully respond to conventional medicine or for which no effective treatment is available. However, no recent reviews of the clinical practice of cupping are available to the best of our knowledge. We describe the applications of CT as used in Traditional Iranian Medicine (TIM). Several databases were searched for relevant literature. In addition, we studied the main traditional treatises on TIM regarding the history and practice of CT. Information about current practices was obtained from a systematic survey among practitioners. Our results suggest that CT is currently prescribed for up to 120 diseases and disorders that are difficult to treat, including cutaneous (21.7%), musculoskeletal (15%), and central nervous system (13.3%) disorders. Moreover, TIM treatises note 25 specific sites on the body surface which correspond to certain diseases, and on which wet-cupping therapy has therapeutic effects. Additional clinical studies of CT may lead to findings on new therapeutic methods and may shed light on mechanisms of disease and illness that are not fully understood in conventional medicine.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 1","pages":"42-7"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000358571","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40288680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The gag reflex is a frequent problem occurring during dental treatment procedures, especially while making impressions of the maxillary teeth. The present study aims to evaluate the efficacy of a simple earplug as an external auditory canal stimulator to supress the profound gag reflex and as a second step, to map areas of the oropharynx suppressed by this technique.
Methods: In the first step of the study, 90 patients who had a gag reflex during the impression procedure were allocated to a study group, a sham group, and a control group for evaluating the efficacy of the earplug technique. Second, 20 new patients with a gag reflex were included in order to map the oropharnygeal areas suppressed by this technique.
Results: The severity of the gag reflex was reduced in the earplug group (but not in the sham or the control group). The affected area included the hard palate, uvula, and the tongue but not the posterior wall of oropharynx.
Conclusion: An earplug technique can be a useful, practical, and effective tool to overcome the gag reflex during oral procedures, such as impression procedures of maxillary teeth.
{"title":"An earplug technique to reduce the gag reflex during dental procedures.","authors":"Yusuf Ozgur Cakmak, Omer Ozdogmus, Yumusan Günay, Bahadır Gürbüzer, Emre Tezulaş, Elif Ciğdem Kaspar, Hüsniye Hacıoglu","doi":"10.1159/000362140","DOIUrl":"https://doi.org/10.1159/000362140","url":null,"abstract":"<p><strong>Background: </strong>The gag reflex is a frequent problem occurring during dental treatment procedures, especially while making impressions of the maxillary teeth. The present study aims to evaluate the efficacy of a simple earplug as an external auditory canal stimulator to supress the profound gag reflex and as a second step, to map areas of the oropharynx suppressed by this technique.</p><p><strong>Methods: </strong>In the first step of the study, 90 patients who had a gag reflex during the impression procedure were allocated to a study group, a sham group, and a control group for evaluating the efficacy of the earplug technique. Second, 20 new patients with a gag reflex were included in order to map the oropharnygeal areas suppressed by this technique.</p><p><strong>Results: </strong>The severity of the gag reflex was reduced in the earplug group (but not in the sham or the control group). The affected area included the hard palate, uvula, and the tongue but not the posterior wall of oropharynx.</p><p><strong>Conclusion: </strong>An earplug technique can be a useful, practical, and effective tool to overcome the gag reflex during oral procedures, such as impression procedures of maxillary teeth.</p>","PeriodicalId":51049,"journal":{"name":"Forschende Komplementarmedizin","volume":"21 2","pages":"94-8"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000362140","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32359334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}