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Novel Mobile Application to Assess Dietary Information

Evaluation of a Novel Mobile Application to Assess Dietary Information

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03578458
Enrollment
132
Registered
2018-07-06
Start date
2018-05-31
Completion date
2018-11-27
Last updated
2019-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Assessment

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.

Interventions

OTHERsubjects will install a mobile app for use

novel mobile application

Sponsors

Société des Produits Nestlé (SPN)
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Energy and nutrient content captured on the mobile applicationDay 1 intakes recorded on application after mealsDuring each eating occasion to report foods and amounts consumed

Secondary

MeasureTime frameDescription
Energy and nutrient content captured on the mobile application by taking photographs of food consumedDay 1 intakes photographed on application after mealsDuring 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 methodUse of application for food capture versus 24 hour dietary recall in reporting foods and amounts consumed

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026