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Evaluation of AI-Mouse Use in Patients With Hand and Wrist Conditions

Evaluation of AI-Mouse Use in Patients With Hand and Wrist Conditions

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07707089
Enrollment
15
Registered
2026-07-16
Start date
2026-07-01
Completion date
2026-10-01
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome (CTS), Hand Injuries, Wounds and Injuries, Hands, Wounds and Injuries, Wrists, Wrist Injuries

Brief summary

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.

Interventions

DEVICEAI-Assisted Computer Input System

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.

DEVICEConventional Computer Mouse

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.

Sponsors

Nazarbayev University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
APDF90 surface electromyography (sEMG) amplitudeBaseline (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.
Muscular rest timeBaseline (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.

Secondary

MeasureTime frameDescription
Integrated squared dynamic accelerationBaseline (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).
90th percentile dynamic accelerationBaseline (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).
Task completion timeBaseline (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.
Error rateBaseline (during each intervention condition on Day 1)Percentage of incorrect target selections during the standardized computer task
Self-reported painImmediately after each intervention condition on Day 1Participant-reported hand and wrist pain after completing each intervention condition, assessed using a numeric rating scale

Contacts

CONTACTJose Berengueres, PhD
jose.berengueres@nu.edu.kz+7 778 358 18 26
CONTACTDina Kalinina, MD
dina.kalinina@nu.edu.kz+77756238719

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026