Dysphagia Clinical Trial
Official title:
The Effect of Simple Swallowing Rehabilitation Training for Elderly Community Dwellers: A Preliminary Study
Verified date | April 2024 |
Source | Chao Phya Abhaibhubejhr Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this clinical trial is to explore the impact of systematic simple swallowing training on swallowing function and quality of life in community-dwelling elderly individuals (≥60 year old) with swallowing disorders. It primarily aims to address two key aspects: 1) the prevalence of dysphagia among community-dwelling elderly individuals, and 2) the effects of systematic simple swallowing training on swallowing function and quality of life in community-dwelling elderly individuals with swallowing disorders. All participants are divided into 2 groups. The intervention group is required to undergo a continuous three-week (21 days) systematic simple swallowing training, with weekends off and training conducted only on weekdays. The training will be conducted two sessions per day, lasting 15-20 minutes each.
Status | Completed |
Enrollment | 248 |
Est. completion date | April 14, 2024 |
Est. primary completion date | April 14, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: - Age over 60 years old. - No hospitalization within the past six months. - With clear consciousness and able to cooperate with questionnaires and training. - The elderly people who voluntarily participate and agree to adhere until the end of the study. - early dysphagia. Exclusion Criteria: - Complicated with severe liver and kidney failure, tumors, or hematological disorders. - Physical disability. - Difficulty in mobility. - Simultaneously receiving other therapies that might influence this study. - Individuals with a gastrostomy. - Abnormalities of the oral, pharyngeal, or esophageal structures. |
Country | Name | City | State |
---|---|---|---|
China | Railway Commu. | Zhenzhou |
Lead Sponsor | Collaborator |
---|---|
Copka Sonpashan |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Gugging Swallowing Screen | The Gugging Swallowing Screen is used to assess dysphagia. The Screen consists of 10 items covering various aspects of swallowing, including oral and pharyngeal muscle function, oral sensation, tongue coordination, and more. The total scores range from 1 to 20, with lower scores indicating more severe dysphagia. | day 1 and day 21 | |
Secondary | Time consumed in eating | We require participants to eat a lunch according to their daily intake and habits, and count the time consumed | day 1 and day 21 | |
Secondary | Swallowing-Related Quality of Life Questionnaire | The Swallowing-Related Quality of Life Questionnaire (SWAL-QOL) is a validated tool used to assess the impact of swallowing difficulties on quality of life. It is a 44-item questionnaire designed to measure the physical, emotional, and social domains of swallowing-related quality of life.The higher final scores indicate the better life quality. The total score will be converted into a standard percentage | day 1 and day 21 | |
Secondary | Eating Assessment Tool-10 | Subjective perception of swallowing function was assessed using the Eating Assessment Tool-10 (EAT-10). The EAT-10 comprises 10 questions that assess various aspects of swallowing function. Each question is scored on a scale from 0 to 4, indicating the severity of swallowing difficulty, with 0 for no difficulty and 4 for severe difficulty. Participants could rate it based on the subjective perception. The total score on the EAT-10 ranges from 0 to 40, with higher scores indicating more severe swallowing disorders. | day 1 and day 21 |
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