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整体数字化体重管理服务联合替西帕肽起始治疗对健康结局的有效性和可持续性:英国一项实用随机对照试验。

The effectiveness and sustainability of health outcomes from a holistic digital weight-loss service with concomitant initiation of tirzepatide: A pragmatic randomized controlled trial in the UK.

机构信息

Faculty of Arts and Social Sciences, University of Sydney, Randwick, Australia.

Medical Research Division, Eucalyptus, Sydney, Australia.

出版信息

Diabetes Obes Metab. 2024 Nov;26(11):4854-4863. doi: 10.1111/dom.15903. Epub 2024 Sep 2.

Abstract

AIM

To measure the effectiveness and sustainability of the Juniper UK digital weight-loss service (DWLS), which delivers 6 months of personalized, proactive lifestyle coaching supplemented with tirzepatide to patients through a multidisciplinary team (MDT).

METHODS

An observer-blinded randomized controlled trial (RCT) will be conducted on a cohort of non-diabetic patients of the Juniper DWLS in the UK. Participants in both the intervention and control groups will receive weekly subcutaneous injections of 2.5 mg tirzepatide for 4 weeks, uptitrating the dose to 5.0 mg from weeks 5 to 8, and by 2.5 mg every 4 weeks until reaching 15 mg in week 21, which they will maintain until the end of the intervention period at 6 months, when participants will be taken off the medication. The intervention group will receive personalized weeklylifestyle coaching with a focus on protein intake and resistance training for 6 months. Participants in the control group will attend a diet and exercise group counselling session at programme inception and will be sent a summary of the session's content at months 2 and 4. Aside from these events, health coaches will only interact with control group participants on a reactive basis. From month 6 to month 12, participants from both groups will no longer have access to their MDTs. The trial's co-primary endpoints include weight loss, fat-free to fat-mass ratio and composite strength measures at 12 months (6 months following the end of treatment), compared with baseline. Secondary endpoints include percentage change in weight, fat-free to fat-mass ratio, and composite strength from baseline to 6 months, side effect incidence, and change in cardiometabolic risk factors at 12 months. Quality of life and programme engagement represent the study's exploratory endpoints.

RESULTS

A total of 688 participants enrolled in the study, with a mean age of 44.6 (± 11.4) years and a mean body mass index of 34.8 (± 7.5) kg/m; 81.0% of participants are women, and 72.8% are of White ethnicity. More than three-quarters of participants have at least one co-morbidity, with dyslipidaemia (42.4%), hypertension (35.3%) and high cholesterol (31.8%) being the most prevalent conditions.

CONCLUSIONS

This RCT will be the first to assess the effectiveness and sustainability of a real-world intensive, multidisciplinary DWLS, and it should highlight the potential of such a service for long-term obesity treatment compared with programmes that deliver standard health counselling.

摘要

目的

评估 Juniper UK 数字减肥服务(DWLS)的有效性和可持续性,该服务通过多学科团队(MDT)为患者提供 6 个月的个性化、主动的生活方式指导,并辅以替西帕肽。

方法

将对英国 Juniper DWLS 的非糖尿病患者队列进行一项观察者盲随机对照试验(RCT)。干预组和对照组的参与者都将接受每周一次的 2.5mg 替西帕肽皮下注射,持续 4 周,从第 5 周到第 8 周剂量增加到 5.0mg,每 4 周增加 2.5mg,直到第 21 周达到 15mg,然后维持到 6 个月的干预期结束,此时参与者将停止用药。干预组将接受为期 6 个月的个性化每周生活方式指导,重点关注蛋白质摄入和抗阻训练。对照组的参与者将在项目开始时参加饮食和运动小组咨询会议,并在第 2 个月和第 4 个月收到会议内容摘要。除了这些活动,健康教练只会在需要时与对照组参与者进行互动。从第 6 个月到第 12 个月,两组参与者都将无法再获得 MDT 的支持。该试验的主要复合终点包括治疗结束后 12 个月(6 个月)的体重减轻、去脂体重与脂肪量的比值和综合力量测量,以及从基线到 6 个月的体重变化、去脂体重与脂肪量的比值、综合力量变化、不良反应发生率和 12 个月时心血管代谢风险因素的变化。生活质量和项目参与度是研究的探索性终点。

结果

共有 688 名参与者入组该研究,平均年龄为 44.6(±11.4)岁,平均体重指数为 34.8(±7.5)kg/m;81.0%的参与者为女性,72.8%为白种人。超过四分之三的参与者至少有一种合并症,最常见的合并症是血脂异常(42.4%)、高血压(35.3%)和高胆固醇血症(31.8%)。

结论

这项 RCT 将首次评估真实世界强化多学科 DWLS 的有效性和可持续性,它应该突出此类服务在长期肥胖治疗方面的潜力,与提供标准健康咨询的方案相比。

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