Actively Recruiting

Age: 70Years +
All Genders
NCT07205354

Design of a Food Preference Assessment Tool for Older Patients in Geriatrics units_DYSPHAGING-PREFERENCES

Led by Hospices Civils de Lyon · Updated on 2025-12-19

209

Participants Needed

3

Research Sites

69 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Swallowing disorders - or oral dysphagia (OD) - are identified as a cause of malnutrition. They gradually lead patients to withdraw certain foods from their diet, leading to progressive dietary imbalances, or increased cardiovascular risks. Two European societies (the European Society for Swallowing Disorders and the European Union Geriatric Medicine Society) have defined recommendations that include raising awareness of OD, the use of screening scores, preventive measures, diagnostic standardization and interventions implemented (re-education, adaptation of textures). We recently reported the results of the DYSPHAGING Pilot Study that validated the feasibility of a standardized care path including a systematic screening of OD and the implementation of preventive measures in geriatric wards. DYSPHAGING Preferences is a three-step research program designed to develop (step 1) a specific device to evaluate food preferences in geriatric populations, adapted from the CFTPQ, evaluate its test-retest reliability (step 2), and perform a cross-sectional study to explore individual differences within the older population depending on their geriatric characteristics and, among them, on the presence or not of OD (step 3).

CONDITIONS

Official Title

Design of a Food Preference Assessment Tool for Older Patients in Geriatrics units_DYSPHAGING-PREFERENCES

Who Can Participate

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged over 70
  • Patient hospitalised in the healthcare sector (CSG, SMR)
  • Patient or patient under guardianship informed of the study and having expressed no objection to participating in the study
  • Patient under guardianship whose guardian has been informed of the study and has expressed no objection to the patient's participation in the study.
Not Eligible

You will not qualify if you...

  • Patient unable to complete the questionnaire.
  • Patient unable to eat orally

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Hopital Pierre GARRAUD Unité de Soins Médicaux et de Réadaptation

Lyon, France, 69005

Not Yet Recruiting

2

Groupement hospitalier Sud Court Séjour de Gériatrie

Pierre-Bénite, France, 69310

Actively Recruiting

3

Groupement hospitalier Sud Unité de Soins Médicaux et de Réadaptation

Pierre-Bénite, France, 69310

Not Yet Recruiting

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Research Team

M

Marion MERDINIAN, Dr

CONTACT

N

Nicolas MASSE-DERAGON

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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