ACTRN12610000773033尚未招募未知
Prescription Procedures for Cochlear Hybrid Devices to optimise the acoustic-to electric output requirements for adults who use a Hybrid device.
The HEARing Cooperative Research Centre Limited0 个研究点目标入组 16 人开始时间: 2010年9月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 16
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 80 Years(—)
- 性别
- All
入选标准
- •1. Will be eighteen years of age or older at the time of evaluation.
- •2. Will be users of a Cochlear Hybrid System with a minimum of 12 months experience prior to enrolment.
- •3. The audiometric criteria for residual hearing in the implanted ear will be within the range of normal to profound.
- •4. A willingness to wear all device conditions (New hearing aids and Hybrid sound processor) on a daily basis for the duration of the study.
- •5. A willingness to participate in and to comply with all requirements of the protocol including a willingness to complete all tests and questionnaires.
排除标准
- •1. Children under the age of 18 years of age.
- •2. People whose primary language is other than English (LOTEs).
- •3. Additional needs or disability that would prevent participation in evaluations.
- •4. Unrealistic expectations on the part of the participant, regarding the possible benefits and limitations of the study.
研究者
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