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一项评价印度“关爱中风”干预措施有效性的随机对照试验方案:一种使用智能手机、由护理人员支持的、针对中风后残疾管理的教育干预措施。

Protocol for a randomised controlled trial to evaluate the effectiveness of the 'Care for Stroke' intervention in India: a smartphone-enabled, carer-supported, educational intervention for management of disabilities following stroke.

机构信息

Public Health Foundation of India, Indian institute of Public Health - Hyderabad, South Asia Centre for Disability, Inclusive Development and Research (SACDIR), Hyderabad, Telangana, India.

Department of Clinical Research, International Centre for Evidence in Disability, London School of Hygiene and Tropical Medicine, London, UK.

出版信息

BMJ Open. 2018 May 9;8(5):e020098. doi: 10.1136/bmjopen-2017-020098.

Abstract

INTRODUCTION

The rising prevalence of stroke and stroke-related disability witnessed globally over the past decades may cause an overwhelming demand for rehabilitation services. This situation is of concern for low-income and middle-income countries like India where the resources for rehabilitation are often limited. Recently, a smartphone-enabled carer-supported educational intervention for management of physical disabilities following stroke was developed in India. It was found to be feasible and acceptable, but evidence of effectiveness is lacking. Hence, as a step forward, this study intends to evaluate clinical effectiveness of the intervention through a randomised controlled trial.

METHODS

The objective of the study is to evaluate whether the 'Care for Stroke' intervention is clinically and cost-effective for the reduction of dependency in activities of daily living among stroke survivors in an Indian setting. This study is designed as a randomised controlled trial comparing people who received the intervention to those receiving standard care. The trial will be pragmatic and outcome assessor-blinded. The primary outcome for the study is dependency in daily living measured by the Modified Rankin Scale (MRS). A total of 266 adult stroke survivors who fulfil the eligibility criteria will be randomised to receive either 'Care for Stroke' intervention or standard treatment and will be followed up for 6 weeks. The main analyses will compare participants allocated to the 'Care for Stroke' intervention versus those allocated to the standard treatment group on an 'intention-to-treat' basis, irrespective of whether the participants received the treatment allocated or not. The dichotomised MRS scores (0-3 and 4-6) in both the groups will be used to calculate the effect estimates with a measure of precision (95% CI) and presented in the results of the trial.

ETHICS AND DISSEMINATION

The Indian Institute of Public Health-Hyderabad/Public Health Foundation of India - Independent Institutional Ethics Committee and the Ethics Committee of the London School of HygieneandTropical Medicine. Dissemination will be through peer-reviewed publications.

TRIAL REGISTRATION NUMBER

Clinical Trial Registry of India CTRI/2017/07/009014.

摘要

简介

在过去几十年中,全球范围内中风及相关残疾的发病率不断上升,这可能导致对康复服务的需求过大。这种情况令人担忧,因为印度等中低收入国家的康复资源往往有限。最近,印度开发了一种基于智能手机的、由照顾者支持的中风后身体残疾管理教育干预措施。研究发现该措施具有可行性和可接受性,但缺乏有效性证据。因此,作为一项前进措施,本研究旨在通过随机对照试验评估该干预措施的临床效果。

方法

本研究的目的是评估在印度环境中,“中风关爱”干预措施是否在减少中风幸存者日常生活活动依赖方面具有临床和成本效益。本研究设计为比较接受干预措施的人与接受标准护理的人的随机对照试验。该试验将具有实用性和结果评估者盲法。研究的主要结局是通过改良 Rankin 量表(MRS)衡量日常生活的依赖程度。共有 266 名符合入选标准的成年中风幸存者将被随机分配接受“中风关爱”干预或标准治疗,并进行 6 周随访。主要分析将比较接受“中风关爱”干预的参与者与接受标准治疗组的参与者的意向治疗分析,无论参与者是否接受了分配的治疗。两组的 MRS 评分(0-3 分和 4-6 分)将用于计算效果估计值,以测量精度(95%置信区间)表示,并在试验结果中呈现。

伦理和传播

印度公共卫生学院-海得拉巴/公共卫生基金会印度独立机构伦理委员会和伦敦卫生与热带医学学院伦理委员会。将通过同行评议的出版物进行传播。

试验注册号

印度临床试验注册中心 CTRI/2017/07/009014。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e85/5942432/312c88b32b3d/bmjopen-2017-020098f01.jpg

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