- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03869658
Food Talk: A New App for Daily Food Monitoring
September 12, 2019 updated by: Susan Roberts, Tufts University
This project will pilot test a new app for self-monitoring food intake using natural spoken language (by voice recognition or text) to provide daily estimates of energy and nutrient intakes with a phone app.
Study Overview
Detailed Description
Self-recording food intake is recommended for weight management and healthy eating.
However, current methods, including web platforms and apps, are often burdensome leading to short-term use by the consumer.
The solution uses cutting-edge speech and language understanding technology to streamline the food logging process.
With this technology, the user simply describes what they ate and the system automatically selects the appropriate items and quantities consumed from the USDA food database, which calculates the nutrition profile of the entry.
Study Type
Observational
Enrollment (Actual)
40
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
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02111
- Human Nutrition Research Center on Aging
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-
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
Potential subjects will be recruited from the local community around Boston, Massachusetts.
Recruitment methods include posting flyers, social and local media advertisements, word of mouth, and emails to HNRCA mailing lists.
Description
Inclusion Criteria:
- Generally healthy men and women 18-65 years if age
- Currently participating in ongoing studies at the HNRCA
- Willing and able to sign written informed consent prior to study entry
- iPhone (iOS 11 or higher) user willing to download the COCO application and record food intake for 5 days
Exclusion Criteria:
- Android or iPhone (iOs 10 or lower) user unable to download and use the COCO application
- Holds a graduate degree in nutrition
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 |
|---|---|---|
|
Change in energy intake using food application COCO
Time Frame: Between days 3 and 7 of the study
|
The primary outcome will be to assess whether food capture using the mobile application is comparable with conventional 24-hour dietary recall.
This will be done by measuring the energy intake (mean of two days) in the two methods.
|
Between days 3 and 7 of the study
|
|
Change in energy intake using 24 hour dietary recall
Time Frame: Between days 3 and 7 of the study
|
The primary outcome will be to assess whether food capture using the mobile application is comparable with conventional 24-hour dietary recall.
This will be done by measuring the energy intake (mean of two days) in the two methods.
|
Between days 3 and 7 of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy of food capture method using mobile application
Time Frame: Between days 3 and 7 of the study
|
The secondary outcome will measure the energy and nutrient content reported by the mobile application over time.
Measured energy intake in a subset of participants in another study that provides dietary intake data will be compared to food intake data using the mobile application.
|
Between days 3 and 7 of the study
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Application feasibility
Time Frame: Betweens days 5 and 7
|
Feasibility of the use of the application to record dietary intake will be measured through a patient satisfaction questionnaire.
|
Betweens days 5 and 7
|
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
- Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of childhood and adult obesity in the United States, 2011-2012. JAMA. 2014 Feb 26;311(8):806-14. doi: 10.1001/jama.2014.732.
- Finkelstein EA, Trogdon JG, Cohen JW, Dietz W. Annual medical spending attributable to obesity: payer-and service-specific estimates. Health Aff (Millwood). 2009 Sep-Oct;28(5):w822-31. doi: 10.1377/hlthaff.28.5.w822. Epub 2009 Jul 27.
- Wang Y, Beydoun MA. The obesity epidemic in the United States--gender, age, socioeconomic, racial/ethnic, and geographic characteristics: a systematic review and meta-regression analysis. Epidemiol Rev. 2007;29:6-28. doi: 10.1093/epirev/mxm007. Epub 2007 May 17.
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)
August 1, 2018
Primary Completion (Actual)
June 1, 2019
Study Completion (Actual)
July 1, 2019
Study Registration Dates
First Submitted
September 19, 2018
First Submitted That Met QC Criteria
March 8, 2019
First Posted (Actual)
March 11, 2019
Study Record Updates
Last Update Posted (Actual)
September 13, 2019
Last Update Submitted That Met QC Criteria
September 12, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 1234 (Department of Defense)
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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