Development of a Mobile Application to Represent Food Intake in Inpatients: Dietary Data Systematization

Abstract

Background Nutritional risk situations related to decreased food intake in the hospital environment hinder nutritional care and increase malnutrition in hospitalized patients and are often associated with increased morbidity and mortality. Objective To develop and test the reliability of a mobile application as a virtual instrument to assess the acceptability and quality of hospital diets for inpatients. Methods: This intra- and interobserver development and reliability study investigated an in-hospital food intake monitoring application based on a validated instrument for patients with infectious diseases who were treated at the Evandro Chagas National Institute of Infectious Diseases (INI/FIOCRUZ). The instrument was sequentially administered to patients 48 h after admission to INI hospital units using the printed instrument (paper) and the tested digital application (ARIETI) simultaneously. The tested reliability factor was the consistency of the method in the digital platform, checking whether the application provided equivalent data to the paper instrument, and finally a statistical analysis plan was performed in the R platform version 4.2.0. This project was authorized by the FIOCRUZ/INI Research Ethics Committee under CAAE 35379820.4.0000.5262. Results The ARIETI was developed and tested for reliability in 70 participants, showing similar ability to show caloric intake in Kcal (p = 1.72 E-03), protein intake (g) (p = 0.006362), the proportion of caloric intake (p = 1.54 E-05), and the protein intake (p = 0.003501) relative to the prescribed goal. The application was superior to the paper-based instrument, accelerating the diagnosis of nutritional risk based on food intake by up to 250 s (50–350 min). Conclusions The ARIETI optimized the time between diagnosis of nutritional risk related to dietary intake and the nutritionist’s decision making, showing an improved ability to maintain information quality compared to the paper-based instrument.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

This project was authorized by the FIOCRUZ/INI Research Ethics Committee under CAAE 35379820.4.0000.5262.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

Yes

Data Availability

Data cannot be shared publicly because of Informed Consent Form that guards the participants information and data. Data are available from the Instituto Nacional de Infectologia (contact via 55 (21) 3865-9602 ) for researchers who meet the criteria for access to confidential data. This observational, prospective study conducted a development and reliability assessment of a technological innovation tool for in-hospital dietary anamnesis, and was approved by the FIOCRUZ/INI Research Ethics Committee (CAAE No. 35379820.4.0000.5262). The tool was tested in patients hospitalized at the FIOCRUZ/INI.

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