Screening the Patient for Oral Intake: Applicability of the Yale Swallow Protocol in Patients Across Disease Categories

Last updated: October 20, 2024
Sponsor: National Taiwan University Hospital
Overall Status: Completed

Phase

N/A

Condition

Heartburn

Treatment

Yale Swallow Protocol

Clinical Study ID

NCT06171165
202401146RINE
  • Ages > 18
  • All Genders

Study Summary

With 98 swallow screening tools already developed, dysphagia remains under-screened and undiagnosed. Even for patients at high risk of oropharyngeal dysphagia (i.e., hospitalized aged, post-stroke, Parkinson's disease, head and neck cancer, or those had ≥ 48 hours of endotracheal intubation), swallow screening is not systematically performed. Nurses, as front-line providers, are bombarded with patients' dysphagia. We witnessed patients' subsequent poor outcomes, including delayed oral intake, dependence on the feeding tube, increased pneumonia, prolonged hospital length of stay, and increased in-hospital.

Despite many calls for nurses to perform bedside screens for timely management, there is a lack of census on what tools to use (98 available, many claimed to be valid) and whether nurses are capable of safely performing these screens, especially when facing across-disease patients. Without a screening tool that is used universally across different diseases to assess whether patients can safely engage in oral intake, clinical healthcare professionals will face significant challenges in conducting the screening. Meanwhile, we found the common, shared items, i.e., consciousness, voice/speech, coughing, oral motor movements, and water drinking tests or swallowing trials, are included in most swallow screening tools, suggesting these items are essential basics for oral intake safely.

Therefore, instead of creating a new screening tool, the aim of this study is to extract the common, shared items among existing swallowing screening tools and assemble them into a swallow screening protocol that can be administered by nursing staff for triage whether inpatient populations are at risk of unsafe for oral intake. After conducting a systematic review and assessing the quality, we found the Yale Swallow Protocol was identified as a high-quality swallowing screening tool and was used for screening the risk of aspiration across diverse outpatients who were referred for further swallow assessment. However, whether the Yale Swallow Protocol can be implemented in acute care settings to screen for "oral intake" requires further warranted for its applicability. Therefore, this study aims to test the applicability (i.e., accuracy, responsiveness, time-spending, and safety) of the Yale Swallow Protocol when used to screen for 'oral intake,' with speech therapists' evaluations serving as the reference standard for inpatients across various disease categories.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Hospitalized patients with any of the following conditions: (a) head-and-neckcancer, (b) stroke, (c) Parkinson's disease, (d) post-extubated, and (e) aged above 65 years.

  • aged above 18 years.

Exclusion

Exclusion Criteria:

  • Patients will be excluded if they are (a) feeding-tube dependent (gastrostomy tube,nasogastric tube), (b) nil per os (NPO), or (c) with airborne-transmitted diseases (e.g., open tuberculosis or SARS).

Study Design

Total Participants: 502
Treatment Group(s): 1
Primary Treatment: Yale Swallow Protocol
Phase:
Study Start date:
February 19, 2024
Estimated Completion Date:
September 06, 2024

Connect with a study center

  • National Taiwan University School of Nursing

    Taipei,
    Taiwan

    Site Not Available

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