Evaluation of the Comparative Efficacy of Navak Guggulu Versus Vachaharidradi Gana Vati in the Management of Sthaulya (Overweight) in Children: Protocol for a Randomized Controlled Trial.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES
Kavita Kishor Fadnavis, Renu Bharat Rathi, Karuna Sunil Ratnaparkhi, Bharat Jagdishji Rathi, Paresh Rameshrao Deshmukh
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引用次数: 0

Abstract

Background: Childhood obesity is a lifestyle-oriented disorder, which may lead to many comorbidities such as hypertension, coronary diseases, increased incidence of diabetes, and metabolic syndromes. Lack of diet control and increased screen time specifically after the COVID-19 pandemic among children and adolescents are the major reasons for this rising global concern. Despite various campaigns being carried out to lessen the rising rates of childhood obesity, the objectives have not yet been achieved. Ayurveda offers a multidimensional modality in managing children with overweight. The purpose of this study is to evaluate the combined efficacy of Ayurvedic medicine administration, diet restriction, and Sun Salutation. Navak Guggulu is a herbo-mineral compound already proven for its antiobesity action. Vachaharidradi Gana mentioned in Ayurvedic classics is a group of herbs, which are Kaphamedohara and Karshana. Ayurveda also emphasizes the importance of diet and physical activities for the treatment of obesity. The interventions together may help in promoting a healthy weight, improving metabolism, and reducing fat accumulation. So, in this study, the efficacy of Vachaharidradi Gana Vati will be compared with Navak Guggulu to treat children with overweight in addition to diet restrictions and Sun Salutation.

Objective: The aim of the study is to evaluate the efficacy of Navak Guggulu versus Vachaharidradi Gana Vati along with diet restriction and Sun Salutation in overweight (Sthaulya) children.

Methods: A double-blind randomized interventional study will be conducted on selected children with overweight in the age group of 10 to 16 years. They will be equally distributed into 2 groups. The control group will be given Navak Guggulu, and the trial group will be given Vachaharidradi Gana Vati for 90 days. Both groups will be advised of diet restrictions and the daily performance of the Sun Salutation. The study duration is 180 days, with assessment at baseline, followed by every 15 days up to 90 days, and at the end point, that is, after 180 days. Appropriate statistical techniques, such as analysis of covariance paired 2-tailed t test, Wilcoxon signed rank test, Mann-Whitney U test, and multivariate regression analysis, will be used to evaluate the efficacy of the interventions.

Results: The study got underway in April 2024. Since participants may begin at any time, our goal is for everyone to be finished by May 2025.

Conclusions: This research will be useful to provide new insight into the effectiveness of the Ayurveda pharmacological approach in treating obesity in children. The results will guide evidence-based multimodality in treatments aimed at changing lifestyle behaviors in children with obesity, thus reducing social stigmatization in them.

Trial registration: Clinical Trial Registry of India CTRI/2023/03/051135; https://ctri.nic.in/Clinicaltrials/pmaindet2.php?EncHid=NzgzNzE=&Enc=&userName=.

International registered report identifier (irrid): DERR1-10.2196/58838.

Navak Guggulu与Vachaharidradi Gana Vati治疗儿童超重的比较疗效评价:一项随机对照试验方案。
背景:儿童肥胖是一种以生活方式为导向的疾病,它可能导致许多合并症,如高血压、冠状动脉疾病、糖尿病发病率增加和代谢综合征。特别是在2019冠状病毒病大流行之后,儿童和青少年缺乏饮食控制和屏幕时间增加,是这一全球担忧日益加剧的主要原因。尽管开展了各种运动以减少儿童肥胖率的上升,但目标尚未实现。阿育吠陀在管理超重儿童方面提供了一种多维模式。本研究的目的是评估阿育吠陀药物管理,饮食限制和日光浴的联合疗效。Navak Guggulu是一种草药矿物化合物,已被证明具有抗肥胖作用。阿育吠陀经典中提到的阿育吠陀经典是一组草药,它们是Kaphamedohara和Karshana。阿育吠陀还强调饮食和体育活动对治疗肥胖的重要性。这些干预措施共同有助于促进健康的体重,改善新陈代谢,减少脂肪堆积。因此,在本研究中,除了饮食限制和Sun Salutation外,Vachaharidradi Gana Vati将与Navak Guggulu治疗超重儿童的疗效进行比较。目的:本研究的目的是评估Navak Guggulu与Vachaharidradi Gana Vati以及饮食限制和日光浴对超重(Sthaulya)儿童的疗效。方法:选择10 ~ 16岁超重儿童进行双盲随机介入研究。他们将被平均分配到两组。对照组服用Navak Guggulu,试验组服用Vachaharidradi Gana Vati,持续90天。两组都将被告知饮食限制和每日做拜日式。研究持续时间为180天,在基线时进行评估,然后每15天进行一次评估,直至90天,并在180天后结束。适当的统计技术,如协方差分析配对双尾t检验、Wilcoxon符号秩检验、Mann-Whitney U检验和多元回归分析,将被用于评估干预措施的有效性。结果:这项研究于2024年4月开始。由于参与者可以在任何时候开始,我们的目标是让每个人在2025年5月之前完成。结论:本研究将有助于为阿育吠陀药物治疗儿童肥胖的有效性提供新的见解。研究结果将指导以证据为基础的多模式治疗,旨在改变肥胖儿童的生活方式行为,从而减少对他们的社会污名化。试验注册:印度临床试验注册中心CTRI/2023/03/051135;https://ctri.nic.in/Clinicaltrials/pmaindet2.php?EncHid=NzgzNzE=&Enc=&userName=.International注册报告标识符(irrid): DERR1-10.2196/58838。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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