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Representations of Oral Nutritional Supplementation (ONS) in Hospitals : Gender differences_observational Study

Representations of Oral Nutritional Supplementation (ONS) in Hospitals : Gender differences_observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03588169
Acronym
CNO_ALIMS
Enrollment
118
Registered
2018-07-17
Start date
2019-01-14
Completion date
2019-02-28
Last updated
2019-10-16

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

Conditions

Malnutrition, Oral Nutritional Supplementation

Brief summary

Over 30% of hospitalized patients are malnourished. These figures range from 20% to 60% in geriatric units. Undernutrition results either from a decrease in energy intake, an increase in needs, an increase in losses or a combination of these three causes. As a factor in mortality, morbidity and lengthening the time of hospital stays, undernutrition induces health costs 45 to 102% higher than a person who is not undernourished. The nutritional management of patients initially includes hygieno-dietary advice, then the implementation of an oral nutritional supplementation (ONS). A recent study conducted by our teams highlighted the low ONS consumption among women compared to men (39.48% vs 73.41%). Interviews with patients showed that 13 out of 17 had a negative opinion of ONS. The aim of this study is to show, on a larger scale, whether ONS consumption differs according to sex and if so, to highlight the obstacles to this consumption through the implementation of semi-directive interviews with patients. Ultimately, this research will lead to the implementation of alternative strategies to improve ONS consumption and to a better understanding of the obstacles to ONS consumption.

Interventions

DIETARY_SUPPLEMENTsemi-structured interviews

About 30 minutes and touching on the following subjects: * perception of hospital meals * patient representation of ONS * taking ONS and feelings about it

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* patient who has given oral consent * over 18 years * orally fed * with a prescription for ONS * speaks and understands French * hospital stay longer than 4 days

Exclusion criteria

* adult under tutelage * pregnant or breastfeeding women * cognitive disorders * patient does not speak or understand French

Design outcomes

Primary

MeasureTime frame
Semi-structured individual interviews1 day on inclusion

Countries

France

Outcome results

None listed

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