Ahern Amy L, Aveyard Paul N, Halford Jason Cg, Mander Adrian, Cresswell Lynne, Cohn Simon R, Suhrcke Marc, Marsh Tim, Thomson Ann M, Jebb Susan A
MRC Human Nutrition Research, Elsie Widdowson Laboratory, Fulbourn Road, Cambridge CB1 9NL, UK.
BMC Public Health. 2014 Jun 18;14:620. doi: 10.1186/1471-2458-14-620.
Recent trials demonstrate the acceptability and short term efficacy of primary care referral to a commercial weight loss provider for weight management. Commissioners now need information on the optimal duration of intervention and the longer term outcomes and cost effectiveness of such treatment to give best value for money.
METHODS/DESIGN: This multicentre, randomised controlled trial with a parallel design will recruit 1200 overweight adults (BMI ≥28 kg/m2) through their primary care provider. They will be randomised in a 2:5:5 allocation to: Brief Intervention, Commercial Programme for 12 weeks, or Commercial Programme for 52 weeks. Participants will be followed up for two years, with assessments at 0, 3, 12 and 24 months. The sequential primary research questions are whether the CP interventions achieve significantly greater weight loss from baseline to 12 months than BI, and whether CP52 achieves significantly greater weight loss from baseline to 12 months than CP12. The primary outcomes will be an intention to treat analysis of between treatment differences in body weight at 12 months. Clinical effectiveness will be also be assessed by measures of weight, fat mass, and blood pressure at each time point and biochemical risk factors at 12 months. Self-report questionnaires will collect data on psychosocial factors associated with adherence, weight-loss and weight-loss maintenance. A within-trial and long-term cost-effectiveness analysis will be conducted from an NHS perspective. Qualitative methods will be used to examine the participant experience.
The current trial compares the clinical and cost effectiveness of referral to a commercial provider with a brief intervention. This trial will specifically examine whether providing longer weight-loss treatment without altering content or intensity (12 months commercial referral vs. 12 weeks) leads to greater weight loss at one year and is sustained at 2 years. It will also evaluate the relative cost-effectiveness of the three interventions. This study has direct implications for primary care practice in the UK and will provide important information to inform the decisions of practitioners and commissioners about service provision.
Current Controlled Trials ISRCTN82857232. Date registered: 15/10/2012.
近期试验表明,将初级保健患者转诊至商业体重管理服务机构进行体重管理具有可接受性且短期有效。目前,医疗服务采购者需要了解最佳干预时长、此类治疗的长期效果及成本效益,以便实现资金的最佳价值。
方法/设计:本多中心平行随机对照试验将通过初级保健机构招募1200名超重成年人(体重指数≥28千克/平方米)。他们将按2:5:5的比例随机分配至:简短干预组、为期12周的商业项目组或为期52周的商业项目组。参与者将接受为期两年的随访,分别在第0、3、12和24个月进行评估。连续的主要研究问题是,商业项目干预在基线至12个月期间的体重减轻幅度是否显著大于简短干预,以及为期52周的商业项目在基线至12个月期间的体重减轻幅度是否显著大于为期12周的商业项目。主要结局将是对12个月时各治疗组间体重差异进行意向性分析。还将通过每个时间点的体重、脂肪量和血压测量以及12个月时的生化风险因素来评估临床疗效。自我报告问卷将收集与依从性、体重减轻和体重维持相关的社会心理因素数据。将从英国国家医疗服务体系(NHS)的角度进行试验期间及长期的成本效益分析。将采用定性方法来考察参与者的体验。
当前试验比较了转诊至商业服务机构与简短干预的临床效果和成本效益。本试验将具体研究在不改变内容或强度的情况下,提供更长时间的体重减轻治疗(12个月商业转诊与12周相比)是否会在一年时带来更大的体重减轻,并在两年时得以维持。它还将评估这三种干预措施的相对成本效益。本研究对英国的初级保健实践具有直接影响,并将为从业者和医疗服务采购者关于服务提供的决策提供重要信息。
国际标准随机对照试验编号ISRCTN82857232。注册日期:2012年10月15日。