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临床试验/NCT04063748
NCT04063748进行中(未招募)不适用

Leuven Interactive Scheme for hearingTraining Evaluation, and Audiological Rehabilitation

Universitaire Ziekenhuizen KU Leuven2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
90
试验地点
2
主要终点
Speech in noise intelligibility

研究概览

简要总结

It is believed that persons with hearing impairment benefit from auditory rehabilitation (AR), i.e. regular assessment and training of their listening skills. However, the efficacy of auditory rehabilitation has not been investigated before. In Leuven (Belgium) an e-health app has been developed that enables performance assessment, listening skills training, and counselling for persons with hearing impairment. Currently, an RCT is prepared to evaluate the different modules in persons with hearing impairment. The experimental group will receive auditory rehabilitation training modules, and a control group will either receive training tasks that are NOT believed to transfer to improved listening skills or will not receive any training (passive control).

  1. Do participants improve on the trained tasks in the LUISTER AR scheme and does this improvement transfer to an improvement in speech perception in noise (primary outcome), executive functioning and/or quality of life (secondary outcomes)?
  2. Does training with the LUISTER AR scheme provide more benefit on primary and secondary outcomes than a placebo program (active control group) or no training (passive control group)?
  3. Can improvement in speech in noise perception, obtained with the LUISTER AR scheme, be consolidated until 6 months after training has stopped?
  4. Are certain user-specific or training-specific aspects correlated to improvement on task-specific learning as well as near- and far transfer

详细描述

Goals of the study:

To determine an optimal, personalized AR scheme (considering age, degree of HI) and possible interacting factors (e.g., training time, type of errors)

To investigate transfer of auditory and auditory-cognitive training to listening skills in everyday life

To develop evidence-based guidelines for clinical AR

A study to assess the efficacy in CI users will start with baseline assessment (speech in noise understanding, LIST sentences and cognitive tests (executive functioning, important for listening skills). This will be followed by 8 weeks of training, an intermediate assessment moment, again 8 weeks of training, and a final evaluation moment. After 6 months follow-up evaluation to investigate retention. This study is comprised of an active training group and an active control group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

The participant does not know whether (s)he receives treatment or placebo. The investigator and the outcomes assessor are blind to this information too. The care provide (speech therapist) would know after communication with the participant.

In case of the HA-study, participants either receive an intervention or do not receive an intervention. Therefore, they cannot be masked.

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • hearing impaired
  • sufficient knowledge of the Dutch language

排除标准

  • cognitively impaired

结局指标

主要结局

Speech in noise intelligibility

时间窗: Change at 16 wks compared to baseline

LIST sentences presented in speech-weighted noise. Participants are required to repeat sentences in noise. The Leuven Intelligibility Sentences Test (LIST, (van Wieringen \& Wouters, 2008)) was specifically designed for speech perception in noise assessment in CI users. The test has a high test-retest reliability and a steep slope making it very sensitive to small improvements in performance. An improvement of 2dB results in a clinically relevant improvement in speech. discrimination in noise. Therefore, the primary endpoint to validate the LUISTER AR scheme will be an improvement of 2dB on speech discrimination in noise.

次要结局

  • Executive functioning: task switching(16 weeks, + 6 months)
  • Executive functioning updating(16 weeks, + 6 months)
  • Self-reported measure(0 weeks, for baseline)
  • Executive functioning inhibition(16 weeks, + 6 months)
  • Transfer of change in speech in noise intelligibility(Change at 6 months post intervention compared to primary outcome)
  • Fluid intelligence(0 weeks, for baseline)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Astrid Van Wieringen, PhD

Professor

Universitaire Ziekenhuizen KU Leuven

研究点 (2)

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