Effects of Wiifit vs Conventional Vestibular Rehabilitation on Dizziness and Balance in Patients With Unilateral Peripheral Vestibular Dysfunction
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 42
- 试验地点
- 1
研究概览
简要总结
Unilateral Peripheral Vestibular Dysfunction (UPVD) causes dizziness, imbalance, vertigo, and reduced quality of life.
Conventional Vestibular Rehabilitation Therapy (cVRT) is effective, while WiiFit-based virtual reality training may further enhance motivation and neuroplasticity.
This study aims to compare WiiFit-based training with conventional rehabilitation in improving balance and reducing dizziness in UPVD patients.
A randomized controlled trial will include participants aged 18-65 meeting specific inclusion and exclusion criteria.
Participants will be randomly divided into two groups: Group A receiving conventional therapy (40 minutes, 3 sessions/week) and Group B receiving WiiFit-based exercises for 4 weeks.
Outcomes will be assessed using DHI, Mini-BESTest, and VADL before and after intervention.
详细描述
Unilateral Peripheral Vestibular Dysfunction (UPVD) is a common vestibular disorder resulting in symptoms such as dizziness, imbalance, vertigo, and postural instability.
These symptoms significantly affect patients' daily functioning and quality of life. Conventional Vestibular Rehabilitation Therapy (cVRT), including gaze stabilization, balance training, and habituation exercises, has proven effective in reducing dizziness and improving balance.
However, newer approaches like virtual reality-based rehabilitation using WiiFit offer interactive, task-oriented, and engaging exercises that may enhance motivation and neuroplasticity, potentially leading to better outcomes.This study aims to compare the effectiveness of WiiFit-based vestibular training and conventional vestibular rehabilitation in improving balance and reducing dizziness in patients with UPVD.
The objective is to determine whether the addition of a virtual reality component can yield superior clinical outcomes compared to traditional therapy.
A randomized controlled trial will be conducted on participants diagnosed with UPVD selected through purposive sampling.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults aged 18-65 years
- •Diagnosed with UPVD (confirmed via Positive Head Thrust Test)
- •Experiencing persistent dizziness or imbalance for >4 weeks after acute onset
- •Able to stand and walk independently
- •VSS total score >12
排除标准
- •Central vestibular disorders (e.g., stroke, multiple sclerosis)
- •Active BPPV (confirmed by Dix-Hallpike Test)
- •Severe visual or MSK impairments affecting balance
- •History of epileptic seizures or motion sickness triggered by video games
- •Participation in other vestibular rehab programs during study period -- Diagnosed with severe cervical spine disease