Oral (Hypo-)Function, General Function and Nutritional Status in Elderly Hospitalized Patients
NCT ID: NCT06557226
Last Updated: 2025-03-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
61 participants
OBSERVATIONAL
2020-09-12
2023-09-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Feeding the Patient at Nutritional Risk: Does the Clinical Outcome Improve?
NCT00440453
Comparison of Outcomes Between Parenteral and Enteral Nutrition
NCT02512224
Post - Hospital Syndrome: Profile of Functional Status by Malnutrition
NCT03126500
Malnutrition in Chinese Hospitalized Patients and Optimizing the Usage of Nutritional Screening Tools
NCT02241746
Oral Nutrition Supplementation in Hospitalized Patients
NCT02624752
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The oral function is classified into 4 stages healthy state, oral frailty, oral hypofunction and oral dysfunction. The classification into the different stages result from an examination of 7 parameters: the oral hygiene, the oral dryness, the occlusal force, the tongue-lip motor function, the tongue pressure, the chewing function and the swallowing function.
This study aims to correlate the oral function with the nutritional status of non-acute hospitalized elders. And to further investigate the correlation between the different parameters defining the oral function and the oral health related quality of life (OHRQoL) as measured by theGeneral Oral Health Assessment Index.
A total 60 participants will be recruited in the University Hospital of Geneva, Loëx rehabilitation center. The investigators will see the patient for 2 visits after informed consent. The first visit will be 45 minutes long and will include a dental examination and an examination of the oral hygiene, the oral dryness, the tongue lip motor function, the tongue pressure, the occlusal force and the swallowing function. Diagnosis for nutrition according to the Glim criteria will be done. Furthermore, the participants will be asked to fill an oral health quality of life questionnaire comprising 12 questions.
Oral hypo function will be defined as a state when 3 or more signs were present from the 7 parameters examined.
Linear multiple regression analysis is used to examine the relationship between the nutritional status and oral function. Spearman's rank correlation coefficient will be used to correlate the oral function score and oral health related quality of life.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
patient with oral hypofunction with 3 impaired oral functional parameters
patient's will receive an oral examination comprising the evaluation of 7 parameters: the oral hygiene, the oral dryness, the occlusal force, the tongue-lip motor function, the tongue pressure, the chewing function and the swallowing function. Oral hypofunction is defined as a state when 3 or more signs were present.
oral and nutritional examination
Participants will receive a comprehensive oral examination, nutritional examination and will fill an oral health related quality of life questionnaire.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
oral and nutritional examination
Participants will receive a comprehensive oral examination, nutritional examination and will fill an oral health related quality of life questionnaire.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Hospitalized in Geneva University Hospitals, in rehabilitation or in long term care (Loëx)
* Able to follow simple instructions and perform the tests
* Understand French and complete or answer the questionnaire
* Give written informed consent
* Consent can be obtained from their next of kin or legal representative if necessary
* Have been admitted into the hospital no longer 15 days before inclusion
Exclusion Criteria
* Poorly-controlled diabetes (Liu et al., 2015)
* Patients with gastro-intestinal diseases or symptoms (nausea, vomiting, diarrhea, constipation) affecting oral intake
* If the patient is taking an antimicrobial treatment at this time.
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Geneva, Switzerland
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Frauke Müller
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Christophe Graf, Pr.
Role: STUDY_DIRECTOR
University Hospital, Geneva
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University clinics of dental medicine
Geneva, Canton of Geneva, Switzerland
Geneva University Hospital
Geneva, Canton of Geneva, Switzerland
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2019-01338
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.