- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05008653
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
Conditions
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:
- Healthy adults
- Has a social security number or Tax ID
- Age 18-65 years of age
- Lives anywhere in the United States of America
- Has been weight-stable (has not lost or gained 10% of body weight) within the past 3 months
- Currently owns a smart phone (Android or iPhone)
- Has owned and used a smart phone for at least 12 months
- Consumes at least 3 meals per day
- Consumes at least 50% of meals that are prepared at/from home vs. outside the home (dine-in restaurants, take-out, etc.)
- Prepares at least 50% of the prepared meals within their household
- Willingness to refrain from participating in any experimental trials during this study period
- Willingness to refrain from having any non-emergency, elective surgeries during the study period
- Willingness to eat different/variety of foods for each meal over the three days of dietary record collection
- Willingness to refrain from consuming meal substitution items (examples: Slimfast shake, Soylent, meal replacement bars) over the three days of dietary record collection
- Willingness to download and use an app linked to their smart phone's camera and photo storage
- 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
- Willingness to refrain from sharing meals with other participants during data collection
- Passes a food matching test on the online screening survey with score >70%.
Exclusion Criteria:
- Currently pregnant or plans to become pregnant several weeks prior to enrollment and during the study period
- History of any type of eating disorder (anorexia nervosa, bulimia, etc.)
- 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
- 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.
Sponsor
Collaborators
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.
General Publications
- Subar AF, Kipnis V, Troiano RP, Midthune D, Schoeller DA, Bingham S, Sharbaugh CO, Trabulsi J, Runswick S, Ballard-Barbash R, Sunshine J, Schatzkin A. Using intake biomarkers to evaluate the extent of dietary misreporting in a large sample of adults: the OPEN study. Am J Epidemiol. 2003 Jul 1;158(1):1-13. doi: 10.1093/aje/kwg092.
- McCullough ML. Dietary assessment in the digital age: the ongoing quest for better methods. Am J Clin Nutr. 2018 Jan 1;107(1):1-2. doi: 10.1093/ajcn/nqx066. No abstract available.
- Timon CM, van den Barg R, Blain RJ, Kehoe L, Evans K, Walton J, Flynn A, Gibney ER. A review of the design and validation of web- and computer-based 24-h dietary recall tools. Nutr Res Rev. 2016 Dec;29(2):268-280. doi: 10.1017/S0954422416000172.
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
Keywords
Other Study ID Numbers
- 1730621
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.
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