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Visual and visual–proprioceptive training improve gait via sensory reweighting after chronic stroke: a randomized controlled trial

Visual and visual–proprioceptive training improve gait via sensory reweighting after chronic stroke: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114339
Enrollment
Unknown
Registered
2025-12-10
Start date
2024-11-10
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Stroke

Interventions

Control Group:Conventional rehabilitation combined with standardized gait training (five sessions per week) and supplemented by time/attention-matched activities (three sessions per week for 30 minute
visual oculomotor training Group:Conventional rehabilitation combined with standardized gait training (five sessions per week) and supplemented by saccadic/smooth pursuit training (three sessions per
visual–proprioceptive integration Group:Conventional rehabilitation combined with standardized gait training (five sessions per week) and supplemented by weight-bearing/weight-shifting training with v

Sponsors

Tianjin University of Sport
Lead Sponsor

Eligibility

Sex/Gender
All
Age
42 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosis of ischemic or hemorrhagic stroke; (2) 10–26 months post-onset and clinically stable. (3) Able to safely complete a 10-m walk and moderate-intensity standing/walking training with minimal assistance. (4) Refractive errors allowed; all assessments and training performed under best optical correction; best-corrected visual acuity = 0.70 logMAR. (5) Able to understand verbal instructions. (6) Provision of written informed consent.

Exclusion criteria

Exclusion criteria: (1) Moderate to severe visual impairment that still compromises safe ambulation despite best correction. (2) Uncontrolled vestibular disorder; significant cervical spine or vertebral artery disease. (3) Clinically meaningful foot drop (peak ankle dorsiflexion < 0° during mid-swing on 3D gait analysis). (4) Significant cervical spine or vertebral artery disease. (5) Uncontrolled epilepsy or a history of photosensitive epilepsy. (6) Cardiopulmonary or circulatory conditions that contraindicate moderate-intensity walking exercise. (7) Severe cognitive or communication impairment. (8) Receipt of specialized vision/vestibular rehabilitation within the past 3 months. (9) Poor adherence or refusal of follow-up.

Design outcomes

Primary

MeasureTime frame
Comfortable gait speed;

Secondary

MeasureTime frame
Step-length symmetry;Center-of-pressure symmetry ratio;Hip, knee, and ankle joint angles;Center of Pressure;Fugl-Meyer Assessment ;Step Length;Berg Balance Scale ;

Countries

China

Contacts

Public ContactQinghua Meng

Tianjin University of Sport

fengxuequan@126.com+86 131 0223 1178

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026