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The "Self Evaluation of Food Intake" (SEFI) as a Screening Test for Hospital Malnutrition in Children Over 10 Years

The "Self Evaluation of Food Intake" (SEFI) as a Screening Test for Hospital Malnutrition in Children Over 10 Years

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04536974
Acronym
SEFI
Enrollment
368
Registered
2020-09-03
Start date
2021-03-10
Completion date
2023-11-08
Last updated
2026-06-12

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

Conditions

Malnutrition, Child

Keywords

MALNUTRITION, CHILDREN, SEFI

Brief summary

The goal is to find a simple tool that can be used by medical and paramedical staff and that is reliable to identify children at risk for malnutrition.

Detailed description

The Ingesta Easy Assessment Score (SEFI®) (formerly "food intake assessment tool or EPA®") is validated in hospitals in adults to detect the risk of malnutrition and guide nutritional management. SEFI® combines a visual analogue scale (VAS) with a visual assessment of the portions consumed (www.sefi-nutrition.com). It comes in the form of a ruler equipped with a cursor and allows a visual assessment, by the patient himself, of his food intake, using an analog scale, or a choice of portions. consumed (see appendix). A score \<7/10 is associated with malnutrition or the risk of malnutrition. The investigators hypothesize that, in pediatric services for children 10 years of age or older, SEFI® would be a feasible and reliable tool for screening for the risk of malnutrition.

Interventions

DIAGNOSTIC_TESTSEFI tool

Detect the risk of malnutrition with the SEFI tool

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 10 to 17 and hospitalized in pediatric or pediatric surgery, regardless of the reason for hospitalization. * Whose holders of parental authority have received information on the protocol and have not expressed their opposition to the child's participation in the study, * Having received information on the protocol and not having expressed opposition to participating in the study.

Exclusion criteria

* Patients whose level of understanding does not allow the use of SEFI®

Design outcomes

Primary

MeasureTime frameDescription
Assess the reliability of SEFI® for detecting the risk of acute malnutrition in pediatrics6 monthrate of agreement between the diagnoses of malnutrition obtained by the SEFI® tool and those obtained by diagnostic tools already validated in children: the Weight to Height ratio (or Waterlow index)

Secondary

MeasureTime frameDescription
reliability of SEFI ® to detect the risk of chronic undernutrition in pediatrics6 monthsrate of agreement between the diagnoses of malnutrition obtained by the SEFI® tool and those obtained by diagnostic tools already validated in children: Weight to Age ratio and Height to Age ratio
feasibility of SEFI®6 monthsPercentage of completion of the test compared to the number of subjects included in the study (if the test is carried out for each person included = 100% feasibility)
correlations of VAS results (score or portions consumed) with occurrence of complications and length of hospital stay9 monthsDuration of hospitalization and complications during hospitalization

Countries

France

Contacts

PRINCIPAL_INVESTIGATORGauthier Foulon, Doctor

Rennes University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026