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一项关于“强化”干预措施的随机对照试验及成本效益评估,该干预旨在维持贫困城市社区中年成年人身体活动量的增加。

A randomised controlled trial and cost-effectiveness evaluation of 'booster' interventions to sustain increases in physical activity in middle-aged adults in deprived urban neighbourhoods.

作者信息

Goyder Elizabeth, Hind Daniel, Breckon Jeff, Dimairo Munyaradzi, Minton Jonathan, Everson-Hock Emma, Read Simon, Copeland Robert, Crank Helen, Horspool Kimberly, Humphreys Liam, Hutchison Andrew, Kesterton Sue, Latimer Nicolas, Scott Emma, Swaile Peter, Walters Stephen J, Wood Rebecca, Collins Karen, Cooper Cindy

机构信息

School of Health and Related Research (ScHARR), University of Sheffield, Sheffield, UK.

Sheffield Clinical Trials Research Unit, University of Sheffield, Sheffield, UK.

出版信息

Health Technol Assess. 2014 Feb;18(13):1-210. doi: 10.3310/hta18130.

Abstract

BACKGROUND

More evidence is needed on the potential role of 'booster' interventions in the maintenance of increases in physical activity levels after a brief intervention in relatively sedentary populations.

OBJECTIVES

To determine whether objectively measured physical activity, 6 months after a brief intervention, is increased in those receiving physical activity 'booster' consultations delivered in a motivational interviewing (MI) style, either face to face or by telephone.

DESIGN

Three-arm, parallel-group, pragmatic, superiority randomised controlled trial with nested qualitative research fidelity and geographical information systems and health economic substudies. Treatment allocation was carried out using a web-based simple randomisation procedure with equal allocation probabilities. Principal investigators and study statisticians were blinded to treatment allocation until after the final analysis only.

SETTING

Deprived areas of Sheffield, UK.

PARTICIPANTS

Previously sedentary people, aged 40-64 years, living in deprived areas of Sheffield, UK, who had increased their physical activity levels after receiving a brief intervention.

INTERVENTIONS

Participants were randomised to the control group (no further intervention) or to two sessions of MI, either face to face ('full booster') or by telephone ('mini booster'). Sessions were delivered 1 and 2 months post-randomisation.

MAIN OUTCOME MEASURES

The primary outcome was total energy expenditure (TEE) per day in kcal from 7-day accelerometry, measured using an Actiheart device (CamNtech Ltd, Cambridge, UK). Independent evaluation of practitioner competence was carried out using the Motivational Interviewing Treatment Integrity assessment. An estimate of the per-participant intervention costs, resource use data collected by questionnaire and health-related quality of life data were analysed to produce a range of economic models from a short-term NHS perspective. An additional series of models were developed that used TEE values to estimate the long-term cost-effectiveness.

RESULTS

In total, 282 people were randomised (control = 96; mini booster = 92, full booster = 94) of whom 160 had a minimum of 4 out of 7 days' accelerometry data at 3 months (control = 61, mini booster = 47, full booster = 52). The mean difference in TEE per day between baseline and 3 months favoured the control arm over the combined booster arm but this was not statistically significant (-39 kcal, 95% confidence interval -173 to 95, p = 0.57). The autonomy-enabled MI communication style was generally acceptable, although some participants wanted a more paternalistic approach and most expressed enthusiasm for monitoring and feedback components of the intervention and research. Full boosters were more popular than mini boosters. Practitioners achieved and maintained a consistent level of MI competence. Walking distance to the nearest municipal green space or leisure facilities was not associated with physical activity levels. Two alternative modelling approaches both suggested that neither intervention was likely to be cost-effective.

CONCLUSIONS

Although some individuals do find a community-based, brief MI 'booster' intervention supportive, the low levels of recruitment and retention and the lack of impact on objectively measured physical activity levels in those with adequate outcome data suggest that it is unlikely to represent a clinically effective or cost-effective intervention for the maintenance of recently acquired physical activity increases in deprived middle-aged urban populations. Future research with middle-aged and relatively deprived populations should explore interventions to promote physical activity that require less proactive engagement from individuals, including environmental interventions.

STUDY REGISTRATION

Current Controlled Trials ISRCTN56495859, ClinicalTrials.gov NCT00836459.

FUNDING

This project was funded by the NIHR Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 18, No. 13. See the NIHR Journals Library website for further project information.

摘要

背景

对于在相对久坐的人群中进行简短干预后,“强化”干预措施在维持身体活动水平提升方面的潜在作用,仍需更多证据。

目的

确定在接受简短干预6个月后,那些通过动机性访谈(MI)方式进行面对面或电话形式的身体活动“强化”咨询的人群,其通过客观测量的身体活动是否增加。

设计

三臂平行组实用优效性随机对照试验,嵌套定性研究、保真度、地理信息系统及健康经济学子研究。使用基于网络的简单随机化程序进行治疗分配,分配概率相等。主要研究者和研究统计人员在最终分析前对治疗分配情况保持盲态。

地点

英国谢菲尔德的贫困地区。

参与者

年龄在40 - 64岁之间、居住在英国谢菲尔德贫困地区且在接受简短干预后身体活动水平有所提高的既往久坐人群。

干预措施

参与者被随机分配至对照组(无进一步干预)或接受两次MI干预,分别为面对面(“完全强化”)或电话形式(“迷你强化”)。干预在随机分组后1个月和2个月进行。

主要结局指标

主要结局是使用Actiheart设备(英国剑桥的CamNtech Ltd公司)通过7天加速度计测量的每日总能量消耗(TEE),以千卡为单位。使用动机性访谈治疗完整性评估对从业者能力进行独立评估。从英国国家医疗服务体系(NHS)的短期视角出发,分析每位参与者的干预成本估计值、通过问卷收集的资源使用数据以及与健康相关的生活质量数据,以生成一系列经济模型。还开发了一系列使用TEE值估计长期成本效益的模型。

结果

总共282人被随机分组(对照组 = 96人;迷你强化组 = 92人,完全强化组 = 94人),其中160人在3个月时至少有7天中的4天加速度计数据(对照组 = 61人,迷你强化组 = 47人,完全强化组 = 52人)。基线与3个月之间每日TEE的平均差异有利于对照组而非联合强化组,但差异无统计学意义(-39千卡,95%置信区间 -173至95,p = 0.57)。尽管一些参与者希望采用更家长式的方法,且大多数参与者对干预和研究的监测及反馈部分表示热情,但支持自主性的MI沟通方式总体上是可接受的。完全强化组比迷你强化组更受欢迎。从业者达到并维持了一致的MI能力水平。到最近市政绿地或休闲设施的步行距离与身体活动水平无关。两种替代建模方法均表明两种干预措施都不太可能具有成本效益。

结论

尽管一些个体确实发现基于社区的简短MI“强化”干预有帮助,但招募和保留率较低,且对有足够结局数据的人群的客观测量身体活动水平缺乏影响,这表明它不太可能是一种对贫困中年城市人群维持近期获得的身体活动增加有效的临床或成本效益干预措施。未来针对中年及相对贫困人群的研究应探索促进身体活动的干预措施,这些措施需要个体较少的主动参与,包括环境干预。

研究注册

当前受控试验ISRCTN56495859,ClinicalTrials.gov NCT00836459。

资助

该项目由英国国家卫生研究院(NIHR)卫生技术评估计划资助,将在《卫生技术评估》全文发表;第18卷,第13期。有关更多项目信息,请访问NIHR期刊图书馆网站。

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