mHealth Intervention for Dementia Prevention through lifestyle Optimisation (MIND-PRO) in a primary care setting: protocol for a randomised controlled trial in people with low SES and/or migration background.

IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMJ Open Pub Date : 2025-02-03 DOI:10.1136/bmjopen-2024-088324
Anne Roos van der Endt, Marieke P Hoevenaar-Blom, Henrike Galenkamp, Martien J H Kas, Esther van den Berg, Ron Handels, Eric P Moll van Charante, Edo Richard
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Abstract

Introduction: The Mobile Health (mHealth) Intervention for Dementia Prevention through lifestyle Optimisation (MIND-PRO) study addresses the increasing prevalence of dementia among populations with lower socio-economic status (SES) and/or a migration background. The study aims to evaluate the effectiveness and implementation of an mHealth intervention designed for self-managing lifestyle modifications with remote coaching to reduce dementia risk factors.

Methods and analysis: This prospective randomised open-label blinded end point (PROBE) trial follows a type 2 hybrid effectiveness-implementation design with a 12-month intervention period. It aims to recruit 692 participants in Dutch primary care. Entry criteria include age 50-75 years, low SES and/or migration background, one or more dementia risk factors (hypertension, dyslipidaemia, diabetes mellitus, physical inactivity, smoking, depression and overweight) or manifest cardiovascular disease and possession of a smartphone. Participants are randomised to a coach-supported, interactive app facilitating self-management of dementia risk factors or to a control app with static health information. The primary effectiveness outcome is a composite score of systolic blood pressure, non-high-density lipoprotein cholesterol and body mass index. Implementation outcomes include coverage, adoption, acceptability, appropriateness, feasibility, fidelity, costs and sustainability of the intervention. Secondary outcomes include the Cardiovascular Risk Factors, Ageing and Dementia risk score and its individual risk factors, and disability, physical activity, depressive symptoms, cognitive functioning and daily distance moved.

Ethics and dissemination: The MIND-PRO trial is funded by the Netherlands Organisation for Health Research and Development (ZonMw, grant number 10510032120004) and approved by the Ethics Committee of Amsterdam UMC (reference: METC 2023.0770). Results are expected in 2026 and will be submitted for publication in a peer-reviewed journal, and presented at scientific conferences.

Trial registration number: ISRCTN92928122.

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初级保健环境中通过生活方式优化预防痴呆症的移动健康干预(MIND-PRO):低社会经济地位和/或移民背景人群的随机对照试验方案。
导读:通过生活方式优化预防痴呆症的移动健康(mHealth)干预(MIND-PRO)研究解决了低社会经济地位(SES)和/或移民背景人群中痴呆症患病率日益增加的问题。该研究旨在评估移动健康干预的有效性和实施情况,该干预旨在通过远程指导进行自我管理生活方式的改变,以减少痴呆症的风险因素。方法和分析:这项前瞻性随机、开放标签、盲法终点(PROBE)试验采用2型混合疗效-实施设计,干预期为12个月。它的目标是招募692名荷兰初级保健的参与者。入选标准包括:年龄50-75岁、低社会经济地位和/或移民背景、一种或多种痴呆风险因素(高血压、血脂异常、糖尿病、缺乏运动、吸烟、抑郁和超重)或明显的心血管疾病和拥有智能手机。参与者被随机分配到一个教练支持的交互式应用程序,促进痴呆风险因素的自我管理,或一个带有静态健康信息的控制应用程序。主要疗效指标是收缩压、非高密度脂蛋白胆固醇和体重指数的综合评分。实施结果包括干预措施的覆盖、采用、可接受性、适当性、可行性、保真度、成本和可持续性。次要结果包括心血管风险因素、衰老和痴呆风险评分及其个体风险因素、残疾、身体活动、抑郁症状、认知功能和每日移动距离。伦理和传播:MIND-PRO试验由荷兰卫生研究与发展组织(ZonMw,资助号10510032120004)资助,并由阿姆斯特丹UMC伦理委员会批准(参考编号:METC 2023.0770)。预计结果将于2026年公布,并将在同行评审的期刊上发表,并在科学会议上发表。试验注册号:ISRCTN92928122。
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来源期刊
BMJ Open
BMJ Open MEDICINE, GENERAL & INTERNAL-
CiteScore
4.40
自引率
3.40%
发文量
4510
审稿时长
2-3 weeks
期刊介绍: BMJ Open is an online, open access journal, dedicated to publishing medical research from all disciplines and therapeutic areas. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around fully open peer review and continuous publication, publishing research online as soon as the article is ready.
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