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Clinical Application of Dynamic and Static Balance Testing and Training System: A Multicenter Randomized Controlled Trial

Clinical Application of Dynamic and Static Balance Testing and Training System: A Multicenter Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111468
Enrollment
Unknown
Registered
2025-10-31
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Unilateral Vestibular Dysfunction

Interventions

dynamic and static balance testing and training system:Participants in the intervention group will undergo training using the dynamic and static balance testing and training system for 20–30 minutes p
traditional vestibular rehabilitation:Participants will undergo traditional vestibular rehabilitation for 20–30 minutes per session, 3–5 times per week, for a duration of 4 weeks.
Observation group:None

Sponsors

Eye and ENT Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Participants voluntarily join the study and sign an informed consent form; (2) Aged between 18 and 70 years; (3) Clinically diagnosed with unilateral vestibular dysfunction and in the decompensated phase (patients report dizziness, vertigo, or unsteady gait within the past 12 months); (4) Dynamic Gait Index (DGI) <= 19 points; (5) Able to understand, cooperate with the training and follow-up, and use the dynamic and static balance testing and training system.

Exclusion criteria

Exclusion criteria: (1) Bilateral vestibular loss or significant central balance disorders (e.g., progressive central nervous system diseases, active stroke, etc.); (2) Severe hip or knee joint disease, or other serious conditions that significantly affect walking; (3) Severe cardiopulmonary disease or other systemic conditions unsuitable for participation in exercise rehabilitation; (4) Receipt of systematic vestibular rehabilitation training within the past 4 weeks; (5) Pregnant or lactating women (adjustable according to local ethical requirements); (6) Any other condition deemed inappropriate for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
Dynamic Balance Function;

Secondary

MeasureTime frame
Vestibular activities and participation measure;Severity of vertigo;Quality of life;Adherence;

Countries

China

Contacts

Public ContactLi Huawei

Eye and ENT Hospital of Fudan University

hwli@shmu.edu.cn+86 189 1778 5659

Outcome results

None listed

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