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Standardized Dysphagia Diet in Clinical Evaluation of Swallowing Function

The Application of Standardized Dysphagia Diet in Clinical Evaluation of Swallowing Function in Dysphagia Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05634980
Enrollment
50
Registered
2022-12-02
Start date
2021-08-03
Completion date
2023-07-31
Last updated
2022-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysphagia, Swallowing Function, Diet Modification, Dysphagia Diet, Diet Standardization

Brief summary

Diet modification has been a vital component in the management of dysphagia. The lingual manipulation of bolus, pharyngeal propulsion, and initiation of swallowing reflex are all affected by the texture of bolus. However, there is a limited literature and consensus regarding how to apply different food consistency in the swallowing function evaluation of dysphagic patients. Recently, International Dysphagia Diet Standardization Initiative (IDDSI) has provided a universal standard of food consistency. The present study aims to evaluate the accuracy of clinical swallowing evaluation using IDDSI standardized food in dysphagic patients, in an attempt to establish protocols of clinical evaluation and diet selection in dysphagic patients.

Interventions

OTHERFEES

Fiberoptic Endoscopic Evaluation of Swallowing (FEES) exam

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 20 years or older with a swallowing disorder on the Functional Oral Intake Scale (FOIS) of 1-6.

Exclusion criteria

* Unconscious, unable to communicate via gestures or words and cooperate with commands. * Acutely infected or requiring respirator use. * The oropharyngeal structure is abnormal and cannot be examined by endoscopy. * Presence of tracheostomy tube

Design outcomes

Primary

MeasureTime frameDescription
Penetration aspiration scale (PAS)Day 1Penetration aspiration scale

Countries

Taiwan

Contacts

Primary ContactMing-Yen Hsiao
myferrant@gmail.com+886223123456

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026