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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03820791
Other study ID # DYSPHAGIA
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 2019
Est. completion date February 2019

Study information

Verified date October 2018
Source Universidade do Porto
Contact Irene P Carvalho, PhD
Phone 225513622
Email irenec@med.up.pt
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date February 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Placement of a poster in patients' rooms
Patients and their caregivers will be exposed to the poster for one month

Locations

Country Name City State
Portugal CINTESIS - Faculty of Medicine of the University of Porto Porto

Sponsors (1)

Lead Sponsor Collaborator
Universidade do Porto

Country where clinical trial is conducted

Portugal, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in patients' aspiration risk before and after placement of the poster in their rooms Change in patients' risk of aspiration in dysphagia (with the Gugging Swallowing Screen - GUSS) 1 month
Primary Change in patients' capacity for oral intake before and after placement of the poster in their rooms Change in patients' oral intake capacity in dysphagia (with the Functional Oral Intake Scale - FOIS) 1 month
Primary Change in patients' oral health before and after placement of the poster in their rooms Change in patients' oral health in dysphagia (with the Oral Health Assessment Tool - OHAT) 1 month
Primary Change in patients' nutritional health before and after placement of the poster in their rooms Change in patients' nutritional status in dysphagia (with the Mini Nutritional Assessment - MNA) 1 month
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