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Surveying Nutrient Assessment With Photographs of Meals (SNAPMe) Study

Surveying Nutrient Assessment With Photographs of Meals (SNAPMe) Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05008653
Acronym
SNAPMe
Enrollment
110
Registered
2021-08-17
Start date
2021-09-01
Completion date
2022-01-29
Last updated
2022-05-13

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

Conditions

Food Characteristics

Keywords

Artificial intelligence, Dietary records, Food systems, Computer science, Sustainability, Nutrition

Brief summary

The SnapMe Study is a single-group, prospective study that requires healthy adults to maintain food diaries in order to develop benchmark data for the prediction of food characteristics.

Detailed description

The purpose of this study is to develop a method that uses photography to accurately calculate the types and amounts of nutrients in meals that are consumed by healthy participants, thereby replacing the use of electronic food records. Researchers expect about 100 healthy individuals at UC Davis and around the U.S. will join to participate in this research. Participation in this study will involve taking pictures of every meal and snack the individual consumes using a smartphone for 3 days (2 weekdays, 1 weekend day) and uploading the images to a mobile phone application called Bitesnap. In addition, the participant will be asked to complete online food records on the same days using the Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24-2020). Each participant will have 4 weeks to complete the study. The study website can be viewed here: https://snapme.ucdavis.edu/

Interventions

None listed

Sponsors

United States Department of Agriculture (USDA)
CollaboratorFED
University of California, Davis
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

1. Healthy adults 2. Has a social security number or Tax ID 3. Age 18-65 years of age 4. Lives anywhere in the United States of America 5. Has been weight-stable (has not lost or gained 10% of body weight) within the past 3 months 6. Currently owns a smart phone (Android or iPhone) 7. Has owned and used a smart phone for at least 12 months 8. Consumes at least 3 meals per day 9. Consumes at least 50% of meals that are prepared at/from home vs. outside the home (dine-in restaurants, take-out, etc.) 10. Prepares at least 50% of the prepared meals within their household 11. Willingness to refrain from participating in any experimental trials during this study period 12. Willingness to refrain from having any non-emergency, elective surgeries during the study period 13. Willingness to eat different/variety of foods for each meal over the three days of dietary record collection 14. Willingness to refrain from consuming meal substitution items (examples: Slimfast shake, Soylent, meal replacement bars) over the three days of dietary record collection 15. Willingness to download and use an app linked to their smart phone's camera and photo storage 16. Willingness to spend 1-2 hours per day on each of the three study days to: 1)enter detailed information about each meal they consume using an online record system and an app on their smart phone and 2) take and upload photos of their meals on their smart phone 17. Willingness to refrain from sharing meals with other participants during data collection 18. Passes a food matching test on the online screening survey with score \>70%.

Exclusion criteria

1. Currently pregnant or plans to become pregnant several weeks prior to enrollment and during the study period 2. History of any type of eating disorder (anorexia nervosa, bulimia, etc.) 3. Use of restrictive diets such as caloric restriction or intermittent fasting of more than 12 hours that has resulted in weight loss greater than 10% of their body weight within the past 3months ordiets 4. Anyone the investigator feels is not an applicable participant.

Design outcomes

Primary

MeasureTime frameDescription
Primary Study Endpoint3 daysConstruct a library with thousands of meals and snacks and images of these meals and snacks.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026