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The Impact of Practicing Active Breathing Exercises on Elderly Individuals Living in the Community

Dysphagia Clinical Trial

Official title:
The Impact of Practicing Active Breathing Exercises on Elderly Individuals Living in the Community: A Preliminary Self-control Study

Clinical Trial Summary

The goal of this clinical trial is to explore the impact of Active Breathing Exercises 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 Active Breathing Exercises on swallowing function and quality of life in community-dwelling elderly individuals with swallowing disorders. All participants enrolled are required to undergo a continuous three-week (21 days) Active Breathing Exercises, with weekends off and training conducted only on weekdays. The training will be conducted two sessions per day, lasting 15-30 minutes each.

Clinical Trial Description

The investigators have designed a simple and user-friendly training method called "Active Breathing Exercises" based on commonly used swallowing training techniques in the department of rehabilitation medicine and the prevalent pathological causes of swallowing disorders in the elderly. The goal of this clinical trial is to explore the impact of Active Breathing Exercises 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 Active Breathing Exercises on swallowing function and quality of life in community-dwelling elderly individuals with swallowing disorders. All participants enrolled are required to undergo a continuous three-week (21 days) Active Breathing Exercises, with weekends off and training conducted only on weekdays. The training will be conducted two sessions per day, lasting 15-30 minutes each. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06328192
Study type Interventional
Source Chao Phya Abhaibhubejhr Hospital
Contact Lavie Ce
Phone 15333828388
Email linchuangzhuce@163.com
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date May 2024
View Details
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