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Under-consumption of FoodENGAGENCT05239442

Engaging Elderly People Living in Institutions in Eating Situations

A study testing Taste Commission, Evaluation of the taste commissions and Entretien SWOT in people with Under-consumption of Food, run by Centre Hospitalier Universitaire Dijon at 1 site in France.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Several recent studies have revealed a significant under-consumption of food in hospitals and nursing homes. For instance, at the Dijon University Hospital, 8 out of 10 patients consume less than 80% of the meals served. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Under-consumption of Food
What is being tested?
Taste Commission, Evaluation of the taste commissions and Entretien SWOT
Could I receive a placebo?
No, everyone receives an active treatment
How many people
640 participants
Where
1 siteFrance
Study dates
29 Mar 2021to Dec 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Hospitalized patients:
  • Person hospitalized in one of the following departments: the endocrinology-diabetology department, geriatric medicine, pulmonology, rheumatology, dermatology, infectious diseases, internal medicine, cardiology, as well as the rehabilitation department, which are departments with an average length of stay sufficient to perform the study
  • Person aged ≥ 50 years (this choice was made because more than 60% of the hospitalized population is currently over 50 years old)
  • Person having given their oral agreement
  • Person with an oral diet and eating without assistance
  • Person with a normal texture diet
Show all 18Show fewer
  • For taste commissions and SWOT interviews: person with sufficient cognitive status to answer questions in a questionnaire or interview (MMSE > 21).
  • Residents in nursing home (EHPAD):
  • Person residing in EHPAD
  • Person aged ≥ 65 years
  • Person having given oral consent
  • Person who is orally fed and self-feeding
  • Person with a normal texture diet
  • For taste commissions and SWOT interviews: person with sufficient cognitive status to answer questions in a questionnaire or interview (MMSE > 21).
  • Facility staff for SWOT interviews:
  • Person who has worked at the facility where the taste commissions were implemented at least 3 months previously.
  • Person who gave oral consent
  • Person between the ages of 18 and 60

Who cannot join

  • Person at the end of life
  • Person with an eating disorder
  • Person with a significant chronic psychiatric disorder (psychosis, manic-depression).
  • Person requiring enteral or parenteral nutrition.
  • Person in a period of exclusion from a previous study

Trial locations and contacts

1 site in 1 country.

France1 site, 1 recruiting
  • Chu Dijon Bourgogne

    Dijon, 21000

    Virginie VAN WYMELBEKE, 03 80 29 31 55, virginie.vanwymelbeke@chu-dijon.fr

    Recruiting

Other trials in France

About this study

Several recent studies have revealed a significant under-consumption of food in hospitals and nursing homes. For instance, at the Dijon University Hospital, 8 out of 10 patients consume less than 80% of the meals served. This has two consequences: an increase in the risk of malnutrition (some patients leave the hospital in such a poor nutritional state that they must be re-hospitalized within six months) and significant food waste. At the heart of this problem, the taste of the food is the subject of frequent and recurrent complaints from users. Although the food industry widely uses sensory methods to adapt its products to the taste of consumers, these methods are rarely used by the organizations that provide meals to care institutions.

The objective is to establish "taste commissions" in the daily practice in institutions for the elderly (hospital, nursing home), in order to improve the organoleptic quality of the meals served according to the expectations and preferences of the users. The principle of this system is to allow the users to taste the dishes produced by the kitchen of the establishment and to transmit these evaluations to the cooks so that they can rework the recipes according to the users' feedback.

Being tested
Taste Commission, Evaluation of the taste commissions, Entretien SWOT

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Taste CommissionOther

    Evaluation of the daily meal once a week:

    Introduction on the different sensory dimensions of the food, hedonic rating for each component, indicate what pleases/what could be improved in the recipe.

  • Evaluation of the taste commissionsOther

    At 0, 3, 6 months:

    • Food intake measurement, satisfaction measurement, and food waste measurement performed on 2 days (same week but not necessarily consecutive)
    • Assessment of nutritional status using the Mini-Nutritional Assessment (MNA)
  • Entretien SWOTOther

    Individual semi-guided face-to-face interview with an experimenter. They will allow us to identify the positive and negative effects of the taste commissions in the establishment as well as the levers and difficulties encountered during the implementation of the taste commissions. These interviews will be recorded using an audio device (dictaphone). Their content will then be transcribed in full.

Study groups in NCT05239442
Study groupRoleWhat they receive
PatientsOtherHospital Patients: - Person hospitalized in one of the following departments: endocrinology-diabetology, geriatric medicine, pulmonology, rheumatology, dermatology, infectious diseases, internal medicine, cardiology, as well as in the rehabilitation department
Receives: Other: Taste Commission; Other: Evaluation of the taste commissions
Institutional staffOtherPerson working in the establishment where the taste commissions have been in place for at least 3 months
Receives: Other: Entretien SWOT
ResidentsOtherPatients residing in nursing home
Receives: Other: Taste Commission; Other: Evaluation of the taste commissions; Other: Entretien SWOT

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. weight of consumed ingesta

    Measured: Change from Baseline to 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Feb 2022
  2. Study start29 Mar 2021
  3. Primary completionMar 2023 (estimated)
  4. Study completionDec 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
640 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05239442
Sponsor's protocol ID
VAN WYMELBEKE I-SITE 2017
Acronym
ENGAGE
Status last verified
Feb 2022
First submitted
27 Oct 2021
Last updated
14 Feb 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Taste Commission, Evaluation of the taste commissions and Entretien SWOT in people with Under-consumption of Food, run by Centre Hospitalier Universitaire Dijon at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 18 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 14 Feb 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Virginie VAN WYMELBEKE (03 80 29 31 55, virginie.vanwymelbeke@chu-dijon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

weight of consumed ingesta (time frame: Change from Baseline to 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Feb 2022.

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