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Preventing Malnutrition and Restoring Nutritional Status in Hospitalized Children

Developing an Organization to Improve the Screening and Care of Starved Children in Hospital

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01081587
Acronym
PREDIRE
Enrollment
1457
Registered
2010-03-05
Start date
2009-10-31
Completion date
2011-10-31
Last updated
2025-12-19

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

Conditions

Nutrition Disorders

Keywords

Non MeSH terms:, Children, Malnutrition, Computer Clinical Decision Support System, Cluster randomized trial, Healthcare workers, Guideline adherence, Patient safety, MeSH terms:, Nutrition Surveys, Secondary Prevention, Pediatrics, Child Care, Health Personnel, Reminder Systems, Intervention Studies, Quality of Health Care

Brief summary

This cluster-randomized trial will evaluate the impact of a multifaceted intervention (including electronic medical alerts) coordinated by a Nutritional Support Team, on adherence to recommended practices for care of starved children, among health personnel of a large university hospital. A key component of the study is to assess whether improved adherence to guidelines leads to a reduction in rates of complications.

Interventions

PROCEDUREAccess to a Computerized Clinical Decision Support System (CCDDS)

Automatic CCDSS will alert physician for each case of malnourished using an algorithm based on age, sex, weight and size of each hospitalized children.

BEHAVIORALEducation of Healthcare workers

Education of the hospital staff to evidence-based practices in malnutrition care will be proposed in the experimental arm. Specific training will be targeted on participants according to their function.

OTHERLocal assistance by a dietician

Assistance will be conducted locally by a local dietician. Periodic multidisciplinary meetings will be attended by the hospital staff belonging to the intervention arm, including the analysis of clinical incidents related to nutrition care.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* medical and surgical units in a large teaching hospital providing pediatric acute care. * any hospital staff with direct patient care who are affiliated with a single unit (includes physicians, nurses, nursing assistants, physiotherapists, dieticians. * all children recorded as malnourished at their entrance in hospital

Exclusion criteria

* neonatal and intensive care units. * any hospital staff with direct patient care who are not affiliated with a single unit. * age under one month, liver or kidney abnormalities, severe heart failure, stay less than 2 days.

Design outcomes

Primary

MeasureTime frame
Adherence to recommended practices (including weigh in, physiotherapy, nutrition survey and monitoring)At least 2 days depending on the hospitalisation time

Secondary

MeasureTime frame
Incidence of complicationsAt least 2 days depending on the hospitalisation time
Nutritional status evolutionAt least 2 days depending on the hospitalisation time
Mean length and cost of stayAt least 2 days depending on the hospitalisation time
Appropriate call-in Nutritional Support TeamAt least 2 days depending on the hospitalisation time

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026