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Poster on Dysphagia-specific Food Procedures: Usability and Impact

Using a Visual Poster Communicating Dysphagia-specific Food Procedures as a Complementary Means of Information to Caregivers in Inpatient Care: Usability and Impact

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03820791
Acronym
DYSPHAGIA
Enrollment
60
Registered
2019-01-29
Start date
2019-01-31
Completion date
2019-02-28
Last updated
2019-01-29

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

Conditions

Dysphagia

Brief summary

The aim of this study is to evaluate the use of a poster containing information on dysphagia-specific food procedures at two levels: utility from the point of view of patients' caregivers, and impact on patients' health. Half the patients will have the poster placed in their room, whereas the other half will not.

Detailed description

Dysphagia is a swallowing disorder that can be associated with clinically relevant complications, and caregivers can play a fundamental role in this process, namely because they feed the patient. However, studies show a lack of professional-caregiver communication in dysphagia, and caregivers' need for more information. Communicating dysphagia-specific food procedures through a visual poster might bridge professional-caregiver communication gaps, with consequences for the patient's health.

Interventions

DEVICEPlacement of a poster in patients' rooms

Patients and their caregivers will be exposed to the poster for one month

Sponsors

Universidade do Porto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Patients with post-acute dysphagia (lesion occurring at least six weeks prior, approximately), * remaining in inpatient care for at least one month after the first moment of data collection, * 18 years of age or older, * receiving regular visits from their family members or caregivers.

Exclusion criteria

* Failing to meet inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Change in patients' aspiration risk before and after placement of the poster in their rooms1 monthChange in patients' risk of aspiration in dysphagia (with the Gugging Swallowing Screen - GUSS)
Change in patients' capacity for oral intake before and after placement of the poster in their rooms1 monthChange in patients' oral intake capacity in dysphagia (with the Functional Oral Intake Scale - FOIS)
Change in patients' oral health before and after placement of the poster in their rooms1 monthChange in patients' oral health in dysphagia (with the Oral Health Assessment Tool - OHAT)
Change in patients' nutritional health before and after placement of the poster in their rooms1 monthChange in patients' nutritional status in dysphagia (with the Mini Nutritional Assessment - MNA)

Countries

Portugal

Contacts

Primary ContactIrene P Carvalho, PhD
irenec@med.up.pt225513622
Backup ContactAntónio Soares, PhD
ajasoares@med.up.pt225513622

Outcome results

None listed

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