The Impact of Diaphragm Training on Dysphagia in Elderly Nursing Home Residents
NCT ID: NCT06393283
Last Updated: 2024-05-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
200 participants
INTERVENTIONAL
2024-04-30
2024-06-30
Brief Summary
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Detailed Description
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The goal of this clinical trial is to explore the Diaphragm Training on swallowing function in Elderly Nursing Home Residents (≥60 year old) with swallowing disorders. It primarily aims to address: the effects of Diaphragm Training on swallowing function and quality of life in Elderly Nursing Home Residents. All participants are divided into 2 groups. The intervention group is required to undergo a continuous three-week (21 days) Diaphragm Training, with weekends off and training conducted only on weekdays. The training will be conducted two sessions per day, lasting 30 minutes each.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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the intervention group
Diaphragm Training will be given twice a day and 30min per time.
Diaphragm Training
Diaphragm training includes both active and passive methods. Passive training involves placing weights on the participant's abdomen to provide resistance during breathing. Active training involves instructing participants to practice diaphragmatic breathing techniques.
the blank group
No intervention will be applied.
No interventions assigned to this group
Interventions
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Diaphragm Training
Diaphragm training includes both active and passive methods. Passive training involves placing weights on the participant's abdomen to provide resistance during breathing. Active training involves instructing participants to practice diaphragmatic breathing techniques.
Eligibility Criteria
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Inclusion Criteria
* 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 caused by sarcopenia.
Exclusion Criteria
* 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.
60 Years
ALL
No
Sponsors
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Copka Sonpashan
OTHER_GOV
Responsible Party
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Copka Sonpashan
Research Director
Principal Investigators
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Louis Wi
Role: STUDY_CHAIR
Site Coordinator of United Medical Group
Central Contacts
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Other Identifiers
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GejiYanglaoyuan
Identifier Type: -
Identifier Source: org_study_id
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