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NCT04866264Completed

Electronic-Nutrition-Optimizer for Personalized Prevention

Source: ClinicalTrials.gov · Last updated 7 Aug 2024

Brief summary (registry, in English)

This study aims to develop and validate a tool for immediate nutrition assessment and to test its user feasibility in routine clinical practice for health promotion.

Status (registry)
Completed
Study type
Interventional
Enrollment
88 (actual)
First submitted
1 Apr 2021
Start date
11 Nov 2021
Primary completion date
23 May 2024
Lead sponsor
Heike Bischoff-Ferrari
NCT number
NCT04866264

What you commit to

  • Study type: Interventional
  • Participants enrolled: 88
  • From 11 Nov 2021 to the primary completion date, 23 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Living in a nursing home and/or receiving prepared meals (i.e. usually not eating home cooked meals)

Other illness

  • Patients following a specific diet recommended by a medical professional, due to diseases such as diabetes, chronic diseases of the gastrointestinal tract, severe kidney disease, or patients allergic to the main components of the Mediterranean diet/MINDdiet (olive oil, nuts)
  • Instable clinical conditions (e.g. acute infection) at enrolment
  • Patients with active cancer (except non-melanoma skin cancer) or current cancer treatment or any other advanced severe disease

Lab values

  • Outpatients: HbA1C ≥6.5% Inpatients: HbA1C ≥6.5% or diagnosed diabetes mellitus if HbA1C is not available in KISIM

Other

  • If already involved in another ongoing interventional clinical trial, except an interaction with this intervention can be excluded
  • People with an impaired short-term memory (MMSE \<24)
  • BMI \> 30 kg/m2
  • Individuals per se not willing to change diet
  • Inability to read and or speak German necessary to understand the instructions

Who the study is looking for

  • Stable inpatients from the Department of heart surgery, or Center for senior trauma patient at the university hospital Zurich (inpatient group)
  • Ambulatory volunteers who can visit the center for aging and mobility (CAM) independently ("outpatients" group)
  • ≥50 years

Age in the registry: 50 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre on Aging and Mobility, University of Zurich
Coordinator of this site? Confirm its status
ZurichSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.