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Setting research priorities to improve the health of children and young people with neurodisability : a British Academy of Childhood Disability-James Lind Alliance Research Priority Setting Partnership

机译:确定研究重点以改善神经残疾儿童和青少年的健康:英国儿童残疾学会-詹姆斯·林德联盟研究重点设定合作伙伴关系

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摘要

Objectives To engage young people, parent carers and clinicians in a systematic process to identify and prioritise research questions regarding ways to improve the health and well-being of children and young people with neurodisability.\ud\udDesign British Academy of Childhood Disability (BACD)-James Lind Alliance research priority setting partnership bringing together patients, carers and clinicians as equal stakeholders.\ud\udSetting UK health service and community.\ud\udMethods The BACD Strategic Research Group formed the partnership. A Steering Group was established; charity and professional partner organisations were recruited. Suggestions were gathered in an open survey and from research recommendations for statutory guidance. Items were aggregated to formulate indicative research questions and verified as uncertainties from research evidence. An interim survey was used to rank the questions to shortlist topics. A mixed group of stakeholders discussed the top 25 questions at the final priority setting workshop agreeing a final rank order and the top 10 research priorities.\ud\udParticipants Partner organisations were 13 charities and 8 professional societies. 369 people submitted suggestions (40% non-clinicians). 76 people participated in the interim prioritisation (26 parents, 1 young person, 10 charity representatives, 39 clinicians); 22 took part in the final workshop (3 young people, 7 parents, 3 charity representatives, 9 professionals).\ud\udResults The top three research priorities related to (1) establishing the optimal frequency and intensity (dose) for mainstream therapies, (2) means for selecting and encouraging use of communication strategies and (3) ways to improve children's attitudes towards disability. The top 10 included evaluating interventions to promote mobility, self-efficacy, mental health, continence, physical fitness, educational inclusion and reduce impacts of sleep disturbance.\ud\udConclusions The methodology provided a systematic and transparent process to identify research priorities that included stakeholders that have typically not contributed to setting the research agenda. The top 10 and other topics identified provide a resource for researchers and agencies that fund research.
机译:目标促使年轻人,家长照顾者和临床医生参与系统的过程,以识别和优先考虑有关改善神经残疾儿童和年轻人的健康和福祉的方法的研究问题。\ ud \ udDesign英国儿童残疾学会(BACD) -詹姆斯·林德联盟(James Lind Alliance)研究重点确定伙伴关系,将患者,护理人员和临床医生平等地视为利益相关者。\ ud \ ud建立英国卫生服务和社区。\ ud \ ud方法由BACD战略研究小组组成。建立了指导小组;募集了慈善机构和专业合作伙伴组织。在公开调查中收集了建议,并从研究建议中收集了建议,以提供法律指导。汇总项目以提出指示性研究问题,并从研究证据中确认为不确定性。进行了一项临时调查,以将问题排在候选名单上。利益相关者混杂在一起,在最终优先级确定研讨会上讨论了前25个问题,同意了最终排名次序和前10个研究优先级。\ ud \ ud参与者合作伙伴组织是13个慈善机构和8个专业协会。 369人提交了建议(非临床医生占40%)。 76人参加了临时优先级排序(26位父母,1位年轻人,10位慈善代表,39位临床医生); 22位参与者参加了最后的讲习班(3位年轻人,7位父母,3位慈善代表,9位专业人员)。\ ud \ ud结果前三项研究重点与(1)确定主流疗法的最佳频率和强度(剂量), (2)选择和鼓励使用沟通策略的手段,以及(3)改善儿童对残疾的态度的方法。前十名包括评估干预措施,以促进行动不便,自我效能感,心理健康,节制,身体健康,教育包容性并减少睡眠障碍的影响。通常对制定研究议程没有贡献的东西。确定的前十个主题和其他主题为资助研究的研究人员和机构提供了资源。

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