Descriptive Study on the Evaluation of Well-being in Relation to Diet and Nutrition and Comparison Between Three Care Units in the Dijon University Hospital Centre
ALIMS
1 other identifier
observational
440
1 country
1
Brief Summary
The aim of this study is to qualify patient well-being in relation to diet. The notion of dietary well-being is believed to be subjective and we wish to base it on tangible parameters (presentation of meals, variety of menus, social interaction, environment, convenience, pleasure...) in order to establish a score of dietary well-being that we will then correlate to the patient's nutritional status. This tool can then be used more widely as an assessment tool within health institutions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2018
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 12, 2018
CompletedFirst Submitted
Initial submission to the registry
April 27, 2018
CompletedFirst Posted
Study publicly available on registry
May 9, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 24, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
July 24, 2018
CompletedNovember 26, 2018
April 1, 2018
6 months
April 27, 2018
November 23, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Questionnaire evaluating well-being in relation to diet and nutrition
Baseline
Study Arms (3)
Patients hospitalized in the cardiology unit
Patients hospitalized in the orthopedic surgery unit
Patients hospitalized in the endocrinology unit
Interventions
Questionnaire evaluating well-being in relation to diet and nutrition
Eligibility Criteria
patients hospitalized in cardiology, orthopaedic surgery or endocrinology departments
You may qualify if:
- person who has given oral consent
- adult
- persons admitted to cardiology, orthopaedic surgery and endocrinology units
- absence of cognitive problems
- oral food intake
You may not qualify if:
- no affiliation to a national health insurance scheme
- current pregnancy
- blended diet
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chu Dijon Bourogne
Dijon, 21000, France
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 27, 2018
First Posted
May 9, 2018
Study Start
January 12, 2018
Primary Completion
July 24, 2018
Study Completion
July 24, 2018
Last Updated
November 26, 2018
Record last verified: 2018-04