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An Exploratory Study on the Rehabilitation Effect of Head-mounted Laser-guided Active Visual-Spatial-Motor Integration Training in Patients with Unilateral Neglect

An Exploratory Study on the Rehabilitation Effect of Head-mounted Laser-guided Active Visual-Spatial-Motor Integration Training in Patients with Unilateral Neglect

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128223
Enrollment
Unknown
Registered
2026-07-16
Start date
2026-07-16
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Stroke

Interventions

Control group:Traditional visual scanning training
Experimental group:Head-mounted laser eye tracking training

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.First clinically diagnosed unilateral cerebral hemisphere stroke (ischemic or hemorrhagic); 2.The course of the disease lasts from 2 weeks to 6 months after onset. 3.Aged 18 to 80 years old; 4.Vital signs are stable, consciousness is clear, and the patient can understand simple instructions (MMSE >= 18 points); 5.Sign a written informed consent form;

Exclusion criteria

Exclusion criteria: 1.Suffering from severe visual impairment, visual field defect or vestibular dysfunction that affects light spot tracking and head movement training; 2.Cervical instability or severe neck diseases make head rotation impossible. 3.Complicated with severe aphasia, dementia or mental illness, unable to cooperate with assessment and training; 4.Combined severe insufficiency of cardiac, pulmonary, hepatic and renal functions, or malignant tumors and other severe diseases that affect survival or cooperation; 5.Local infections, damage, hypertrophic scars and other conditions on the head that make wearing head-mounted devices unsuitable; 6.Participating in other clinical trials that may affect the results of this study;

Design outcomes

Primary

MeasureTime frame
Kathleen Berg Scale (CBS);The traditional sub-test section of the Behavior Impairment Scale (BIT) (BIT-C);

Secondary

MeasureTime frame
Timed Up and Go Test;Intervention Completion Rate;Recruitment rate;Berg Balance Scale;Patient satisfaction;Therapist Acceptance;Morse Fall Assessment Scale;Fugl-Meyer Upper Limb Motor Function Scale;Patient compliance;Simple Upper Limb Function Test;Stroke-specific Quality of Life Scale (SS-QOL);Modified Barthel Index;Types and incidence rates of adverse events;

Countries

China

Contacts

Public ContactFeng Xiaojuan

Beijing Bo'ai Hospital

460570828@qq.com+86 10 8756 9536

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026