Evaluation of AI-Mouse Use in Patients With Hand and Wrist Conditions
2026年7月10日 更新者：Nazarbayev University
People with hand and wrist conditions, such as carpal tunnel syndrome or hand injuries, often experience pain and discomfort when using a computer mouse.
This study will evaluate a new artificial intelligence (AI)-assisted computer input system ("AI-mouse") designed to reduce the amount of hand movement needed during computer tasks.
Participants will complete short computer-based tasks using both a conventional mouse and the AI-assisted system while researchers measure task performance, muscle activity using surface electromyography (EMG), and participants' ratings of pain, physical strain, and usability.
The study aims to determine whether the AI-assisted system can reduce physical effort and muscle load while maintaining effective computer interaction.
Findings may help improve accessible computer technologies and support the development of ergonomic tools for people with hand and wrist impairments.
研究概览
地位
尚未招聘
研究类型
介入性
注册 (估计的)
15
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Jose Berengueres, PhD
- 电话号码：+7 778 358 18 26
- 邮箱：jose.berengueres@nu.edu.kz
研究联系人备份
- 姓名：Dina Kalinina, MD
- 电话号码：+77756238719
- 邮箱：dina.kalinina@nu.edu.kz
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Adults aged 18-65 years
- Diagnosis of a hand or wrist condition, including carpal tunnel syndrome or hand/wrist injury.
- Receiving care at the Hand Surgery Department of the National Scientific Center of Traumatology and Orthopedics.
- Medically stable and assessed by a study physician as able to safely perform light computer-based hand movements.
- Able to understand the study procedures and provide written informed consent.
- Normal or corrected-to-normal vision sufficient to complete computer-based tasks.
Exclusion Criteria:
- Severe pain or acute symptoms that may be aggravated by computer task performance.
- Postoperative restrictions limiting hand or wrist movement.
- Severe motor impairment preventing completion of the study tasks.
- Cognitive or neurological disorders that interfere with understanding study procedures or task performance.
- Uncorrected visual impairment that interferes with computer use.
- Any medical condition that, in the opinion of the study physician, would make participation unsafe.
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：支持治疗
- 分配：非随机化
- 介入模型：交叉作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器：Conventional Mouse
Participants perform standardized computer pointing tasks using a conventional computer mouse.
Performance (task completion time, error rate, throughput), surface electromyography (EMG) of upper-limb muscles, and participant-reported outcomes (pain, physical strain, and usability) are assessed during task completion.
|
A standard computer mouse used for conventional point-and-click interaction.
Participants complete the same standardized computer tasks as in the experimental condition, allowing direct comparison of task performance, upper-limb muscle activity measured by surface electromyography (EMG), and participant-reported pain, physical strain, and usability.
|
|
实验性的：AI-Mouse (Preview-Accept-Discard [PAD] System)
Participants perform the same standardized computer tasks using the AI-Mouse, a predictive human-computer interaction system based on the Preview-Accept-Discard (PAD) paradigm.
The system generates AI-assisted action suggestions that can be accepted or discarded using minimal keyboard input, reducing cursor movement.
Performance, surface electromyography (EMG), and participant-reported outcomes (pain, physical strain, and usability) are assessed during task completion.
|
A non-invasive computer input system that uses artificial intelligence to predict the user's intended on-screen action.
Instead of relying primarily on continuous cursor movement and mouse clicking, the system presents predicted actions that participants can preview, accept, or discard using minimal keyboard input.
The intervention is designed to reduce repetitive hand movements during computer interaction while preserving user control.
Participants complete standardized computer tasks using the system during a single study session lasting less than four minutes.
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
APDF90 surface electromyography (sEMG) amplitude
大体时间：Baseline (during each intervention condition on Day 1)
|
90th percentile amplitude probability distribution function (APDF90) of the processed sEMG envelope recorded from selected upper-limb muscles during standardized computer tasks.
|
Baseline (during each intervention condition on Day 1)
|
|
Muscular rest time
大体时间：Baseline (during each intervention condition on Day 1)
|
Percentage of task duration during which the processed sEMG envelope remained below the predefined muscular-rest threshold of 2 µV.
|
Baseline (during each intervention condition on Day 1)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Integrated squared dynamic acceleration
大体时间：Baseline (during each intervention condition on Day 1)
|
Cumulative dynamic movement workload measured by tri-axial accelerometry and expressed as integrated squared dynamic acceleration (mG²·s).
|
Baseline (during each intervention condition on Day 1)
|
|
90th percentile dynamic acceleration
大体时间：Baseline (during each intervention condition on Day 1)
|
Peak dynamic movement intensity measured by tri-axial accelerometry and expressed as the 90th percentile of dynamic acceleration (mG).
|
Baseline (during each intervention condition on Day 1)
|
|
Task completion time
大体时间：Baseline (during each intervention condition on Day 1)
|
Time required to complete the standardized computer task using the conventional mouse and the AI-assisted computer input system.
|
Baseline (during each intervention condition on Day 1)
|
|
Error rate
大体时间：Baseline (during each intervention condition on Day 1)
|
Percentage of incorrect target selections during the standardized computer task
|
Baseline (during each intervention condition on Day 1)
|
|
Self-reported pain
大体时间：Immediately after each intervention condition on Day 1
|
Participant-reported hand and wrist pain after completing each intervention condition, assessed using a numeric rating scale
|
Immediately after each intervention condition on Day 1
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年7月1日
初级完成 (估计的)
2026年9月1日
研究完成 (估计的)
2026年10月1日
研究注册日期
首次提交
2026年6月30日
首先提交符合 QC 标准的
2026年7月10日
首次发布 (实际的)
2026年7月16日
研究记录更新
最后更新发布 (实际的)
2026年7月16日
上次提交的符合 QC 标准的更新
2026年7月10日
最后验证
2026年7月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.