{"title":"姜黄-博斯韦利亚制剂(rhuleaf - k)对姿势相关腰痛和不适的影响:一项随机双盲安慰剂对照试验。","authors":"Ajay Gupta, Alok Agarwal","doi":"10.1177/10538127241296343","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Poor posture from work or lifestyle habits is a common cause of low back soreness and discomfort. This study investigates the potential of Rhuleave-K, a turmeric-Boswellia formulation for managing these symptoms.</p><p><strong>Objective: </strong>To evaluate the efficacy of Rhuleave-K (500 mg) over 15 days in alleviating posture-related low back soreness and discomfort in human participants.</p><p><strong>Methods: </strong>This randomized, placebo-controlled, double-blinded, parallel arm study involved 52 subjects aged 18-70 years, with an equal male to female ratio of 1:1, and a 15 days intervention period. The inclusion criteria were a posture-related low back soreness and discomfort for at least 2-3 weeks with a pain intensity of greater than or equal to 5 on numerical rating scale. The primary outcome measure was a pain intensity difference from baseline to day 7 and day 15. Secondary outcome measures were a categorical pain relief scale and Oswestry disability index (ODI).</p><p><strong>Results: </strong>There was a significant decrease in the pain intensity (p < 0.001) compared to placebo at the end of 15 days of study in the Rhuleave-K group. After 7 days of supplementation of Rhuleave-K, there was a 56% reduction in pain intensity and by the end of the study, there was 98.5% reduction. In the responder profile of those having greater than or equal to 50% of max total pain relief, all 26 was in Rhuelave-K group and 3 were in placebo group. The ODI had significant 27% and 98% reduction in the disability index at day 7 and 15 respectively for Rhuleave-K group and placebo group had 1% and 3% change.</p><p><strong>Conclusion: </strong>Posture-related low back soreness and discomfort was significantly reduced by Rhuleave-K at 500 mg dose. It is hence evident from this study's outcome that the Rhuleave-K can be a safe and effective alternative for the short-term management of lower back discomfort.</p>","PeriodicalId":15129,"journal":{"name":"Journal of Back and Musculoskeletal Rehabilitation","volume":" ","pages":"10538127241296343"},"PeriodicalIF":1.4000,"publicationDate":"2025-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The effect of turmeric-Boswellia formulation (Rhuleave-K) in posture-related low back soreness and discomfort: A randomized double blinded placebo controlled trial.\",\"authors\":\"Ajay Gupta, Alok Agarwal\",\"doi\":\"10.1177/10538127241296343\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Poor posture from work or lifestyle habits is a common cause of low back soreness and discomfort. This study investigates the potential of Rhuleave-K, a turmeric-Boswellia formulation for managing these symptoms.</p><p><strong>Objective: </strong>To evaluate the efficacy of Rhuleave-K (500 mg) over 15 days in alleviating posture-related low back soreness and discomfort in human participants.</p><p><strong>Methods: </strong>This randomized, placebo-controlled, double-blinded, parallel arm study involved 52 subjects aged 18-70 years, with an equal male to female ratio of 1:1, and a 15 days intervention period. The inclusion criteria were a posture-related low back soreness and discomfort for at least 2-3 weeks with a pain intensity of greater than or equal to 5 on numerical rating scale. The primary outcome measure was a pain intensity difference from baseline to day 7 and day 15. Secondary outcome measures were a categorical pain relief scale and Oswestry disability index (ODI).</p><p><strong>Results: </strong>There was a significant decrease in the pain intensity (p < 0.001) compared to placebo at the end of 15 days of study in the Rhuleave-K group. After 7 days of supplementation of Rhuleave-K, there was a 56% reduction in pain intensity and by the end of the study, there was 98.5% reduction. In the responder profile of those having greater than or equal to 50% of max total pain relief, all 26 was in Rhuelave-K group and 3 were in placebo group. The ODI had significant 27% and 98% reduction in the disability index at day 7 and 15 respectively for Rhuleave-K group and placebo group had 1% and 3% change.</p><p><strong>Conclusion: </strong>Posture-related low back soreness and discomfort was significantly reduced by Rhuleave-K at 500 mg dose. 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引用次数: 0
摘要
背景:工作或生活习惯造成的不良姿势是导致腰痛和不适的常见原因。本研究调查了潜在的大黄- k,姜黄-波斯韦利亚配方管理这些症状。目的:评估rhuleleaf - k (500 mg)在15天内缓解人类参与者姿势相关的腰痛和不适的疗效。方法:本研究采用随机、安慰剂对照、双盲、平行组研究,52例年龄18-70岁,男女比例1:1,干预期15天。纳入标准是与姿势相关的腰背疼痛和不适持续至少2-3周,疼痛强度在数值评定量表上大于或等于5。主要结局指标是疼痛强度从基线到第7天和第15天的差异。次要结果测量是分类疼痛缓解量表和Oswestry残疾指数(ODI)。结果:大鼠腰痛强度明显降低(p)。结论:500 mg剂量的大黄叶k可明显减轻与姿势相关的腰痛和不适。因此,从这项研究的结果可以明显看出,rhuleaf - k可以是一种安全有效的短期治疗下背部不适的替代方案。
The effect of turmeric-Boswellia formulation (Rhuleave-K) in posture-related low back soreness and discomfort: A randomized double blinded placebo controlled trial.
Background: Poor posture from work or lifestyle habits is a common cause of low back soreness and discomfort. This study investigates the potential of Rhuleave-K, a turmeric-Boswellia formulation for managing these symptoms.
Objective: To evaluate the efficacy of Rhuleave-K (500 mg) over 15 days in alleviating posture-related low back soreness and discomfort in human participants.
Methods: This randomized, placebo-controlled, double-blinded, parallel arm study involved 52 subjects aged 18-70 years, with an equal male to female ratio of 1:1, and a 15 days intervention period. The inclusion criteria were a posture-related low back soreness and discomfort for at least 2-3 weeks with a pain intensity of greater than or equal to 5 on numerical rating scale. The primary outcome measure was a pain intensity difference from baseline to day 7 and day 15. Secondary outcome measures were a categorical pain relief scale and Oswestry disability index (ODI).
Results: There was a significant decrease in the pain intensity (p < 0.001) compared to placebo at the end of 15 days of study in the Rhuleave-K group. After 7 days of supplementation of Rhuleave-K, there was a 56% reduction in pain intensity and by the end of the study, there was 98.5% reduction. In the responder profile of those having greater than or equal to 50% of max total pain relief, all 26 was in Rhuelave-K group and 3 were in placebo group. The ODI had significant 27% and 98% reduction in the disability index at day 7 and 15 respectively for Rhuleave-K group and placebo group had 1% and 3% change.
Conclusion: Posture-related low back soreness and discomfort was significantly reduced by Rhuleave-K at 500 mg dose. It is hence evident from this study's outcome that the Rhuleave-K can be a safe and effective alternative for the short-term management of lower back discomfort.
期刊介绍:
The Journal of Back and Musculoskeletal Rehabilitation is a journal whose main focus is to present relevant information about the interdisciplinary approach to musculoskeletal rehabilitation for clinicians who treat patients with back and musculoskeletal pain complaints. It will provide readers with both 1) a general fund of knowledge on the assessment and management of specific problems and 2) new information considered to be state-of-the-art in the field. The intended audience is multidisciplinary as well as multi-specialty.
In each issue clinicians can find information which they can use in their patient setting the very next day.