Faculty of Arts and Social Sciences, University of Sydney, Randwick, Australia.
Medical Research Division, Eucalyptus, Sydney, Australia.
Diabetes Obes Metab. 2024 Nov;26(11):4854-4863. doi: 10.1111/dom.15903. Epub 2024 Sep 2.
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).
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.
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.
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.
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。
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。
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%)。
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。