首页> 外文期刊>薬理と治療 >ローヤルゼリーならびにビーエナジー⑧を用いた アンケー卜による食品の有効性の 網羅的評価方法の検証
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ローヤルゼリーならびにビーエナジー⑧を用いた アンケー卜による食品の有効性の 網羅的評価方法の検証

机译:使用蜂王浆和B能量通过问卷调查对食品有效性的综合评价方法的验证⑧

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Objectives The aim of this study was to validate the use of questionnaires as food supplements efficacy evaluation method. Methods Five hundred healthy volunteers (men and women) aged 20-80 years were randomly divided into a protease treated Royal jelly (p-RJ) group (?=250) and a Bee energy? group (n=250). Four g of p-RJ/day or 3 g/day Bee energy? were administered for 8 weeks to each group. Written questionnaires about the present health condition and blood pressure measurements were performed before and after intake. Results The results obtained for p-RJ group showed that the symptoms like dizziness, chest pains, itchiness, arthralgia, irritation, and lumbago were significantly improved く 0.05). The tinnitus and cold intolerance symptoms that already reported of efficacy in other studies have been ameliorated by RJ intake(P=0.13). The Bee energy? group evaluation pointed out a considerable decrease of symptoms like dizziness, tinnitus, palpitations, insomnia, eye strain, constipation and dysuria く0.05). Both groups showed the reduction of systolic blood pressure after intake (p-RJ group, P=0.046 ; Bee energy? group, P=0.053). Conclusions The beneficial effects of p-RJ intake have been recomfirmed with questionnaires, so this method could be considered an effective food evaluation method with minimum costs. Additionally, the useful information obtained from these questionnaires may lead to future strategies for other clinical trials.
机译:目的本研究的目的是验证问卷作为食品补充剂功效评估方法的用途。方法将年龄在20-80岁之间的500名健康志愿者(男女)随机分为蛋白酶治疗的蜂王浆(p-RJ)组(?= 250)和Bee energy?疗法。组(n = 250)。 4克p-RJ /天或3克/天蜂能量?每组服用8周。在摄入之前和之后进行有关当前健康状况和血压测量的书面问卷。结果p-RJ组的结果表明,头晕,胸痛,瘙痒,关节痛,刺激性和腰痛等症状得到明显改善(improved 0.05)。 RJ摄入已改善了其他研究中已报道疗效的耳鸣和寒冷耐受性症状(P = 0.13)。蜜蜂的能量?小组评估指出,头晕,耳鸣,心,失眠,眼疲劳,便秘和排尿困难等症状明显减轻(く0.05)。两组均显示摄入后收缩压降低(p-RJ组,P = 0.046; Bee energy?组,P = 0.053)。结论问卷已重新确认了摄入p-RJ的有益效果,因此该方法被认为是一种成本最低的有效食品评估方法。此外,从这些调查表中获得的有用信息可能会导致其他临床试验的未来策略。

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