MedPath

Novel Mobile Application to Assess Dietary Information

Not Applicable
Completed
Conditions
Dietary Assessment
Interventions
Other: subjects will install a mobile app for use
Registration Number
NCT03578458
Lead Sponsor
Société des Produits Nestlé (SPN)
Brief Summary

The study will assess the accuracy of food capture methods using a novel mobile application. This will be done by comparing the energy and nutrient content of reported foods against those of foods actually consumed (i.e., reported vs actual). Two methods of using the application will be tested:

1. During each eating occasion to report foods and amounts consumed

2. By taking photographs of every food consumed, using the camera functionality of the mobile application and using the application the following day (according to the availability of the study subjects) to report foods and amounts consumed. This is to be consistent with the concept of a 24-hour dietary recall.

One group will use a standard 24-hour dietary recall method.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
132
Inclusion Criteria
  • Generally healthy men and women 18-65 years of age
  • Eats a wide variety of foods from all food groups
  • 18 ≤ body mass index (BMI) < 30 kg/m2
  • Ability to read and write in English
  • iPhone (iOS 11 or higher) or Android phone (6 or higher) user willing to download the mobile application
Exclusion Criteria
  • Presence of active disease at screening that would prevent normal dietary intake and/or would result in weight loss (irritable bowel syndrome, Crohn's disease, celiac disease, etc.)
  • Medical complications or chronic illness that would prevent full participation (e.g., active cancer)
  • Pregnant or lactating women
  • Diagnosed eating disorder
  • Vegetarian
  • Special dietary requirements or severe allergies that prevent the consumption of major food groups (e.g., gluten free, lactose free, Halal)
  • Diagnosis of a mental health condition that has not been stable within the past 6 months
  • Current or previous experience with dietary data collection or analysis
  • Concurrent participation in another research study at any point during the study
  • Availability and access to a tablet device (iPad, Android) only
  • Shift workers
  • Plan to partake in vigorous physical training/ exercise during the study period (e.g., training for or running a marathon)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vegetarian dietsubjects will install a mobile app for useSubjects will install a mobile app for use and will be randomly assigned to a vegetarian diet.
US Healthy dietsubjects will install a mobile app for useSubjects will install a mobile app for use and will be randomly assigned to a healthy diet.
Mediterranean dietsubjects will install a mobile app for useSubjects will install a mobile app for use and will be randomly assigned to a Mediterranean diet.
Primary Outcome Measures
NameTimeMethod
Energy and nutrient content captured on the mobile applicationDay 1 intakes recorded on application after meals

During each eating occasion to report foods and amounts consumed

Secondary Outcome Measures
NameTimeMethod
Energy and nutrient content captured on the mobile application by taking photographs of food consumedDay 1 intakes photographed on application after meals

During each eating occasion to report foods and amounts consumed

Assess whether food capture using the mobile application is comparable with a conventional 24-hour recall.Day 1 intakes will be reviewed by recall method

Use of application for food capture versus 24 hour dietary recall in reporting foods and amounts consumed

Trial Locations

Locations (1)

Tufts University USDA Human Nutrition Research Center on Aging (HNRCA)

🇺🇸

Boston, Massachusetts, United States

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