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Intervention of Diet Registration Method for Rehabilitation Patients

NCT04738682 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2022-11-04

No results posted yet for this study

Summary

Study aims to investigate whether dietary registration can be performed with greater precision using digital registration units (mobile devices), rather than conventional paper based dietary registers.

Study intervention is based in the M3 rehabilitation unit, as part of Hobro hospital. The intervention will proceed until 6 full-day dietary registrations have been collected per patient (40 patients total), 3 for each registration method. The estimated time requirement is 30 days.

Conditions

  • Digital Clinical Diet Registrations Advantages
  • Patients in Rehabilitation

Interventions

OTHER

Digital dietary registration

The purpose of the intervention is to test whether digital dietary registration can yield more precise and consistent data, than conventional pen and paper based registration. Furthermore a subjective evaluation of the use of digital registration will be conducted by the staff upon completion of the intervention. The format will be individual interviews held by the investigators.

OTHER

Conventional dietary registration

The conventional way of doing dietary registration. This is done by a paper form, with the dietary options listed. The form is then filled in and logged by staff working in the afternoon.

Sponsors & Collaborators

  • Movesca ApS

    collaborator UNKNOWN

  • Departmen for rehabilitation M3, Hobro Hospital

    collaborator UNKNOWN

  • University of Copenhagen

    lead OTHER

Principal Investigators

  • Nicolaj Nørlem, MSc · University of Copenhagen

  • Ted Rasmussen, MSc · University of Copenhagen

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-15
Primary Completion
2021-03-15
Completion
2021-07-01

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04738682 on ClinicalTrials.gov