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临床试验/NCT07690709
NCT07690709已完成不适用

Eye Tracking as an Early Cognitive Intervention for Older Adults With Subjective Memory Complaints

Chinese University of Hong Kong2 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2023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
78
试验地点
2
主要终点
Inhibitory control

研究概览

简要总结

The goal of this clinical trial is to learn if a computerized eye-tracking training program can improve mental health and thinking skills in older adults. The main questions it aims to answer are whether eye-tracking training can lower depressive and anxiety symptoms in older adults, and whether it can improve their ability to control impulses and pay attention.

Researchers will compare older adults who receive eye-tracking training to older adults on a waitlist to see if eye-tracking training leads to greater improvements in mood and thinking skills.

Researchers will randomly assign participants into the experimental group or the waitlist control group. Participants in the experimental group will take part in eye-tracking training three times a week for 18 sessions, over about 1.5 months. Before and after training, participants will answer questions about their mood and take tests of memory, attention, and impulse control. Older adults on the waitlist will complete the same tests but will not receive training until after the study period; they will be offered the same training once their waiting period ends.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Community-dwelling Chinese older adults aged 60 to 80 years
  • Able to understand Cantonese/Chinese
  • Normal or corrected-to-normal vision
  • Willing and able to commit to attending 18 training sessions over the course of the intervention

排除标准

  • A history of learning disability, psychiatric disorders, neurological disorders (e.g., head injury or Parkinson's disease), visual and/or hearing impairments, or any other physical disabilities that would affect their performance on neuropsychological assessment or adherence to the intervention
  • Prior or concurrent participation in other interventions involving eye-tracking techniques
  • Signs of dementia, as indicated by a total score of 18 or below on the Hong Kong version of Montreal Cognitive Assessment (HK-MoCA)
  • Inability to commit to the full course of 18 training sessions

结局指标

主要结局

Inhibitory control

时间窗: Baseline and after completion of 18 training sessions (approximately 9 weeks)

Inhibitory Control Index (ICI) in the Eriksen Flanker Test

Sustained attention

时间窗: Baseline and after completion of 18 training sessions (approximately 9 weeks)

Digit Cancellation Index (DCI) in the Digit Cancellation Test

Depressive symptoms

时间窗: Baseline and after completion of 18 training sessions (approximately 9 weeks)

Depressive symptoms are assessed using the 15-item Chinese version of Geriatric Depressive Scale (CGDS-15). It is a 15-item self-report scale in which participants answer "Yes" or "No" to whether they experienced each of 15 common depressive symptoms in the past week. Scores range from 0 to 15, with higher scores indicating more depressive symptoms. A score of 8 or higher indicates clinically significant depressive symptoms.

Anxiety symptoms

时间窗: Baseline and after completion of 18 training sessions (approximately 9 weeks)

Anxiety symptoms are assessed using the 10-item Chinese version of Geriatric Anxiety Scale (CGAS-10). It is a 10-item self-report measure of anxiety symptoms in older adults. Higher scores indicate greater severity of anxiety symptoms.

次要结局

未报告次要终点

研究者

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

Professor Chan Sui-yin Agnes

Professor

Chinese University of Hong Kong

研究点 (2)

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