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Status unknownNCT05634980Updated Dec 2, 2022

Standardized Dysphagia Diet in Clinical Evaluation of Swallowing Function

An observational study in Dysphagia, Swallowing Function, Diet Modification, Dysphagia Diet, Diet Standardization, sponsored by National Taiwan University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2022-12-02.

Sponsored by National Taiwan University Hospital · Observational

The sponsor has not verified this record recently (last verified Nov 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
50
Ages
20 Years and older
Sex
All
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Study 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.

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Conditions studied

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

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03

In context

Deglutition Disorders

710 studies on the registry are indexed under Deglutition Disorders; 219 are open to participants now.

This study's planned enrollment of 50 is below the median of 97 across 207 observational studies indexed under Deglutition Disorders.

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Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with a swallowing disorder

Inclusion criteria

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

Exclusion criteria

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
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No

Interventions

  • OtherFEES

    Fiberoptic Endoscopic Evaluation of Swallowing (FEES) exam

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What researchers measure

Primary outcomes

  1. Penetration aspiration scale (PAS)

    Penetration aspiration scale

    Time frame: Day 1

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Study locations

1 of 1 sites recruiting
  • National Taiwan University Hospital
    Taipei, 100, Taiwan
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 2, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05634980
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Dec 2, 2022
Start date
Aug 3, 2021
Primary completion
Jul 31, 2023 (estimated)
Completion
Jul 31, 2023 (estimated)
Last update
Dec 2, 2022

Study contacts

Ming-Yen Hsiao
Contact
myferrant@gmail.com
+886223123456 ext. 67316

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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