A Randomized Controlled Study to Explore the Effect of Virtual Reality Therapy on Dysphagia in Wallenberg Syndrome
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- standardized swallowing assessment
研究概览
简要总结
The goal of this clinical trial is to learn about on dysphagia in wallenberg syndrome. The main questions it aims to answer are:
the efficacy of Virtual Reality Therapy in the rehabilitation of patients with dysphagia in Wallenberg syndrome.
Participants received conventional dysphagia treatment and Virtual Reality Therapy once a day for 14 days. Researchers compared the control group to see the effect and mechanism of Virtual Reality Therapy.
详细描述
Virtual Reality technology has revolutionized various fields, and its application in rehabilitation medicine is particularly noteworthy. Virtual Reality provides immersive environments that simulate real-life situations, making it an invaluable tool in the rehabilitation process.
The goal of this clinical trial is to learn about on dysphagia in wallenberg syndrome. The main questions it aims to answer are:
the efficacy of Virtual Reality Therapy in the rehabilitation of patients with dysphagia in Wallenberg syndrome.
Participants received conventional dysphagia treatment and Virtual Reality Therapy once a day for 14 days. Researchers compared the control group to see the effect and mechanism of Virtual Reality Therapy.
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
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •age ranged from 18-85 years and right-handed;
- •first onset, vital signs stable and conscious;
- •the dysphagia confirmed by videofluoroscopic swallowing study;
- •no cognitive impairment, the mini-mental state examination score: >17 for those with an illiterate education, >20 for those with an elementary education, and >24 for those with a secondary education and above;
- •cranial integrity without craniotomy and/or craniectomy;
- •patient and/or his/her relative agrees and signs written informed consent.
排除标准
- •combined ischemic foci at other sites;
- •presence of organic swallowing dysfunction or pre-existing dysphagia due to Parkinson's disease, dementia, and others;
- •severe cardiac, pulmonary, hepatic, and renal insufficiency and vital organ failure;
- •infected or broken skin on the head;
- •poorly controlled epilepsy;
- •poor patient compliance.
研究组 & 干预措施
The experimental group
conventional dysphagia treatment and Virtual Reality Therapy are provided
干预措施: Virtual Reality Therapy (Device)
The experimental group
conventional dysphagia treatment and Virtual Reality Therapy are provided
干预措施: Conventional dysphagia treatment (Behavioral)
The control group
conventional dysphagia treatment is provided
干预措施: Conventional dysphagia treatment (Behavioral)
结局指标
主要结局
standardized swallowing assessment
时间窗: day 1 and day 14
The standardized swallowing assessment was used to assess the improvement of overall swallowing function, it has a maximum score of 46 and a minimum score of 18, with lower scores indicating better swallowing function.
次要结局
- Rosenbek penetration-aspiration scale(day 1 and day 14)
- swallowing-quality of life(day 1 and day 14)
- Murray secretion scale(day 1 and day 14)
研究者
Zeng Changhao
Research Director
People's Hospital of Zhengzhou University