Surveying Nutrient Assessment With Photographs of Meals (SNAPMe) Study (SNAPMe)

May 12, 2022 updated by: University of California, Davis
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.

Study Overview

Status

Completed

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/

Study Type

Observational

Enrollment (Actual)

110

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Davis, California, United States, 95616
        • University of California, Davis

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Healthy adults living anywhere in the United States of America between the ages of 18 and 65.

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Primary Study Endpoint
Time Frame: 3 days
Construct a library with thousands of meals and snacks and images of these meals and snacks.
3 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2021

Primary Completion (Actual)

January 28, 2022

Study Completion (Actual)

January 29, 2022

Study Registration Dates

First Submitted

June 28, 2021

First Submitted That Met QC Criteria

August 9, 2021

First Posted (Actual)

August 17, 2021

Study Record Updates

Last Update Posted (Actual)

May 13, 2022

Last Update Submitted That Met QC Criteria

May 12, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Food Characteristics

3
Subscribe