Validation of the CONUT Software Tool for Screening Clinical Malnutrition in the University Hospital La Paz
1 other identifier
observational
233
1 country
1
Brief Summary
Nutrition Department of University Hospital La Paz decided to implement some method of screening in our centre which allowed us to detect as many patients with malnutrition risk as possible. Due to the large size of our centre, with about 1,500 beds and the few human resources in our unit, we chose to use the CONUT system (Nutritional Control), a 100% automatic method based on analytical parameters, very easy to use, low cost and whose validity is confirmed, characteristics that fulfilled our needs. The implementation of this nutritional screening method has led to a change in the ìnutritionafi culture of our centre respect to DRM in most of our professionals: doctors and nurses and even in the management team, so all of them understand the importance of the process and know about the available tools and knowledge to indicate an adequate and early nutritional support.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2012
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
July 15, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2012
CompletedFirst Submitted
Initial submission to the registry
September 12, 2019
CompletedFirst Posted
Study publicly available on registry
September 13, 2019
CompletedSeptember 13, 2019
August 1, 2019
2 months
September 12, 2019
September 12, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
To detect as many patients with malnutrition risk as possible
The method collects information from databases of Admission Service (affiliation, age, date) and Laboratory (albumin, cholesterol, total lymphocytes) and generates, in the report of analytical results, "alert" information about each patient's nutritional risk and also nutritional recommendations based on the risk identified. Prior to its implantation several evaluations were performed in order to allow us to better know the extra workload, as it was the main factor that could limit our ability to assume that screening method and also many training activities for doctors and hospital health professionals who were increasingly assuming responsibilities in the nutritional treatment of their patients.
Three months
Interventions
CONUT has been working from june of 2010 and it has detected risk of malnutrition in 32% of the evaluated patients. The method collects information from databases of Admission Service (affiliation, age, date) and Laboratory (albumin, cholesterol, total lymphocytes) and generates, in the report of analytical results, "alert" information about each patient's nutritional risk and also nutritional recommendations based on the risk identified.
Eligibility Criteria
Cross-sectional study in which the nutritional status of patients will be assessed in the first 72 hours of entry.
You may qualify if:
- Patients of both sexes
- Patients older than 15 years
- Patients admitted to the General Hospital or Traumatology area
- Patients who have signed the informed consent to participate in the study
You may not qualify if:
- Pregnant women.
- Patients whose physical and / or psychic capacity prevents them from providing all the data collected by the evaluated methods or who do not have a caregiver.
- Non-collaborating patients in data collection
- Patients in whom a hospital stay of less than 48 hours is expected.
- Patients who at the time of performing the analyzes are in the ICU and OER
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Institute for Health Research IdiPAZ
Madrid, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Carmen Gómez Candela, Msc
Hospital Universitario La Paz
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 12, 2019
First Posted
September 13, 2019
Study Start
July 15, 2012
Primary Completion
September 15, 2012
Study Completion
December 31, 2012
Last Updated
September 13, 2019
Record last verified: 2019-08