跳至主要内容
临床试验/NCT04696835
NCT04696835招募中不适用

Use of Near-infrared Functional Spectroscopy (fNIRS) in the Evaluation of Hearing Rehabilitation in Children With Hearing Aid(s)

University Hospital, Lille2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年9月9日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40
试验地点
2
主要终点
Oxygenated haemoglobin concentration (HbO)

研究概览

简要总结

Pilot phase. Monocentric, non-controlled, non-randomized, open-label study evaluating the capacity of the functional near-infrared functional neuroimaging (fNIRS) technique to translate temporal cortical activity in response to a speech stimulus in normo-hearing and deaf children with cochlear implants.

Hemodynamic changes are expected to be observed that indicate brain activity following the stimuli, resulting in a change in the concentration of oxygenated hemoglobin (HbO) and deoxygenated hemoglobin (HbR) recorded by the fNIRS.

The use of the FNIRS in the evaluation of hearing aid effectiveness could contribute to a more adapted management of childhood hearing loss since conventional methods in young children are not adapted to the needs of children with hearing loss.

研究设计

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

入排标准

年龄范围
3 Months 至 18 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Group A: Infants and toddlers 3-18 months of age who are normal hearing.
  • Group B: Infants and toddlers aged 3 to 18 months with sensorineural hearing loss fitted with a unilateral or bilateral hearing aid with optimized adjustments by the hearing healthcare professional.
  • Socially insured subject
  • Parents or guardians who have given their consent to participate in the study

排除标准

  • Medical condition that does not allow for research compliance.

结局指标

主要结局

Oxygenated haemoglobin concentration (HbO)

时间窗: Baseline (at inclusion)

次要结局

  • HbR Concentration(At 3 months, 6 months, 12 months and 24 months)
  • Deoxygenated haemoglobin concentration (HbR)(Baseline (at inclusion))
  • HbO Concentration(At 3 months, 6 months, 12 months and 24 months)

研究者

发起方
University Hospital, Lille
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验