NCT03555461CompletedNot Applicable
Analysis of EPA® (a Food Intake Assessment Tool) as a Screening Test for Malnutrition in General Medicine
Rennes University Hospital3 sites in 1 country563 target enrollmentStarted: January 22, 2018Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 563
- Locations
- 3
- Primary Endpoint
- presence or absence of malnutrition
Study Overview
Brief Summary
The main objective is to evaluate the sensitivity of the EPA® for screening for malnutrition in general medicine in adults.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •To be an adult,
- •Consulting the principal investigator, a general practitioner in his activity of substitute doctor,
- •During the inclusion period,
- •Not opposed to participating in the study.
Exclusion Criteria
- •Patients benefiting from artificial nutrition,
- •Patients with advanced dementia,
- •Pregnant or postpartum women,
- •Patients who do not understand or speak French,
- •Patients treated with diuretics who have had a change in treatment dosage during the last 6 months,
- •Patients for whom weight measurement is not possible in the office (wheelchair, disability ...),
- •Patients who have already been included once,
- •Patients who have had surgery for obesity,
- •Major persons subject to legal protection (legal safeguards, guardianship, tutorship), persons deprived of their liberty, ...
Outcomes
Primary Outcomes
presence or absence of malnutrition
Time Frame: The inclusion day
presence or absence of malnutrition based on BMI and / or percentage of weight loss
Score EPA
Time Frame: The inclusion day
score obtained with the EPA® tool (assessment of food intake)
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (3)
Loading locations...
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