跳至主要内容
临床试验/KCT0012354
KCT0012354进行中(未招募)不适用

Development of an artificial intelligence -based model to predict themechanism of cognitive impairment caused by hearing loss and the effect of cognitive functionprotection by auditory rehabilitation

Asan Medical Center0 个研究点目标入组 140 人开始时间: 2026年7月31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
140

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational
观察模型
Cohort, Time Perspective : Prospective, Enrollment : 140, Biospecimen Retention : Not collect nor Archive

入排标准

年龄范围
50(Year) 至 No Limit(—)
性别
All

入选标准

  • 1.Subjects aged 50 years or older.
  • 2.Patients who have visited the Department of Neurology and have been diagnosed with subjective cognitive decline (SCD), mild cognitive impairment (MCI), or early-stage dementia (Clinical Dementia Rating [CDR] = 1).
  • 3.Patients who have visited the Department of Otolaryngology and have moderate-to-severe hearing loss, but are capable of undergoing cognitive assessment with the assistance of hearing aids.
  • 4.Patients with no contraindications to brain magnetic resonance imaging (MRI) or positron emission tomography (PET).
  • 5.Patients who are able and willing to participate in follow-up assessments throughout the 2-year study period.

排除标准

  • 1.Subjects with clinically significant findings that, in the opinion of the Principal Investigator or Sub-Investigator, make MRI examination inappropriate.
  • 2.Subjects with medical conditions that preclude MRI or PET imaging (e.g., claustrophobia).
  • 3.Subjects who are expected to be lost to follow-up within the 2-year study period.
  • 4.Subjects who, in the judgment of the investigator, are not suitable for participation in this clinical study or whose participation may increase the risk associated with the study.

研究者

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