跳至主要内容
临床试验/NCT03316287
NCT03316287已完成不适用

EVidenced Based Management of Hearing Impairments: Public Health pΟlicy Making Based on Fusing Big Data Analytics and simulaTION

University College, London1 个研究点 分布在 1 个国家目标入组 1,080 人开始时间: 2018年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,080
试验地点
1
主要终点
Change in "Glasgow Hearing Aid Benefit Profile" at 8 weeks

研究概览

简要总结

Hearing Loss (HL) affects over 5% of the world's population (WHO 2014) and is the 5th leading cause of Years Lived with Disability. HL is currently managed with Hearing Aids (HAs), i.e. programmable sound amplification devices that are worn by the hearing impaired subjects to address their hearing difficulties. HA use however is often problematic, costly and with poor overall benefits. The holistic management of HL requires appropriate public health policies for HL prevention, early diagnosis, long-term treatment and rehabilitation; detection and prevention of cognitive decline; and socioeconomic inclusion of HL patients. Currently the evidential basis for forming such policies is limited.

The EVOTION project proposes to address this by collecting and analysing a big set of heterogeneous data, including HA usage, audiological, physiological, cognitive, clinical and medication, personal, behavioural, life style, occupational and environmental data.

This will be done by:

i. accessing big datasets of existing HA user data from the EVOTION clinical partners (UCL/UCLH and GST in the UK; OTICON in Denmark) ii. collection of prospective HA user data who will be recruited to the prospective EVOTION study and who will undergo some additional assessments iii. collection of real time dynamic data of the human participant HA users who will be given a smart phone with different apps (auditory tests; auditory training), sensors (recording of heart rate, blood pressure, respiratory rate etc.) and smart HAs (recording environmental factors such as noise levels, type of noise etc.) so that real life contextual factors that affect HA usage and outcome can be identified.

These data will be analysed with big data analysis/data mining techniques in order to identify relationships between these in order to use this information to derive and support public health decisions.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age >18 years
  • Basic understanding of oral and written English
  • Unilateral and/or bilateral mild to severe sensorineural hearing loss
  • Willing to use smart hearing aids for at least 2 hours daily on average
  • Willing/capable to use a mobile phone

排除标准

  • Dementia (MoCA<22 )
  • Not agreeing or able to attend for f/u appointments
  • Not agreeing or able to use HA >2 hours daily (average)
  • Not sufficient vision to use smartphone ap

结局指标

主要结局

Change in "Glasgow Hearing Aid Benefit Profile" at 8 weeks

时间窗: Baseline (i.e. before the patient receives a hearing-aid) and at 8 weeks after receiving a hearing-aid

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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